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Previous release (v1)
2025-07-16 04:13:38, GGRNA.v2 : RefSeq release 229 (Mar, 2025)
LOCUS NM_001161346 11228 bp mRNA linear PRI 09-JUN-2024
DEFINITION Homo sapiens checkpoint with forkhead and ring finger domains
(CHFR), transcript variant 3, mRNA.
ACCESSION NM_001161346
VERSION NM_001161346.2
KEYWORDS RefSeq; MANE Select.
SOURCE Homo sapiens (human)
ORGANISM Homo sapiens
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi;
Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini;
Catarrhini; Hominidae; Homo.
REFERENCE 1 (bases 1 to 11228)
AUTHORS He,F., Ye,B., Wu,X., Pan,J., Wang,J. and Wang,X.
TITLE CHFR promotes metastasis of human gastric carcinoma by activating
AKT and ERK via NRF2- ROS axis
JOURNAL BMC Gastroenterol 23 (1), 114 (2023)
PUBMED 37024798
REMARK GeneRIF: CHFR promotes metastasis of human gastric carcinoma by
activating AKT and ERK via NRF2- ROS axis.
Publication Status: Online-Only
REFERENCE 2 (bases 1 to 11228)
AUTHORS Hagiwara,T., Sugimoto,K., Momose,H., Irie,T., Honjo,K.,
Okazawa,Y.U., Kawai,M., Kawano,S., Munakata,S., Takahashi,M.,
Kojima,Y., Serizawa,N., Nagahara,A., Hoffman,R.M., Brock,M.V. and
Sakamoto,K.
TITLE CHFR-Promoter-Methylation Status Is Predictive of Response to
Irinotecan-based Systemic Chemotherapy in Advanced Colorectal
Cancer
JOURNAL Anticancer Res 42 (2), 697-707 (2022)
PUBMED 35093868
REMARK GeneRIF: CHFR-Promoter-Methylation Status Is Predictive of Response
to Irinotecan-based Systemic Chemotherapy in Advanced Colorectal
Cancer.
REFERENCE 3 (bases 1 to 11228)
AUTHORS Lu,Q., Li,Y., Lou,J., Li,P., Gu,Y. and Wang,X.
TITLE Circ-CHFR modulates the proliferation, migration, and invasion of
ox-LDL-induced human aorta vascular smooth muscle cells through the
miR-214-3p/PAPPA axis
JOURNAL Clin Hemorheol Microcirc 80 (4), 399-412 (2022)
PUBMED 34842180
REMARK GeneRIF: Circ-CHFR modulates the proliferation, migration, and
invasion of ox-LDL-induced human aorta vascular smooth muscle cells
through the miR-214-3p/PAPPA axis.
REFERENCE 4 (bases 1 to 11228)
AUTHORS Wu,W., Zhao,J., Xiao,J., Wu,W., Xie,L., Xie,X., Yang,C., Yin,D. and
Hu,K.
TITLE CHFR-mediated degradation of RNF126 confers sensitivity to PARP
inhibitors in triple-negative breast cancer cells
JOURNAL Biochem Biophys Res Commun 573, 62-68 (2021)
PUBMED 34388456
REMARK GeneRIF: CHFR-mediated degradation of RNF126 confers sensitivity to
PARP inhibitors in triple-negative breast cancer cells.
REFERENCE 5 (bases 1 to 11228)
AUTHORS Luo,H., Zhou,Z., Huang,S., Ma,M., Zhao,M., Tang,L., Quan,Y.,
Zeng,Y., Su,L., Kim,J. and Zhang,P.
TITLE CHFR regulates chemoresistance in triple-negative breast cancer
through destabilizing ZEB1
JOURNAL Cell Death Dis 12 (9), 820 (2021)
PUBMED 34462429
REMARK GeneRIF: CHFR regulates chemoresistance in triple-negative breast
cancer through destabilizing ZEB1.
Publication Status: Online-Only
REFERENCE 6 (bases 1 to 11228)
AUTHORS Sanbhnani,S. and Yeong,F.M.
TITLE CHFR: a key checkpoint component implicated in a wide range of
cancers
JOURNAL Cell Mol Life Sci 69 (10), 1669-1687 (2012)
PUBMED 22159584
REMARK GeneRIF: CHFR is thought to contribute towards regulating mitotic
entry and possible explanations for contradictory observations
published on the functions and regulation of CHFR are presented.
[review]
Review article
REFERENCE 7 (bases 1 to 11228)
AUTHORS Mizuno,K., Osada,H., Konishi,H., Tatematsu,Y., Yatabe,Y.,
Mitsudomi,T., Fujii,Y. and Takahashi,T.
TITLE Aberrant hypermethylation of the CHFR prophase checkpoint gene in
human lung cancers
JOURNAL Oncogene 21 (15), 2328-2333 (2002)
PUBMED 11948416
REFERENCE 8 (bases 1 to 11228)
AUTHORS Chaturvedi,P., Sudakin,V., Bobiak,M.L., Fisher,P.W., Mattern,M.R.,
Jablonski,S.A., Hurle,M.R., Zhu,Y., Yen,T.J. and Zhou,B.B.
TITLE Chfr regulates a mitotic stress pathway through its RING-finger
domain with ubiquitin ligase activity
JOURNAL Cancer Res 62 (6), 1797-1801 (2002)
PUBMED 11912157
REMARK GeneRIF: Chfr regulates a mitotic stress pathway through its
RING-finger domain with ubiquitin ligase activity.
REFERENCE 9 (bases 1 to 11228)
AUTHORS Kang,D., Chen,J., Wong,J. and Fang,G.
TITLE The checkpoint protein Chfr is a ligase that ubiquitinates Plk1 and
inhibits Cdc2 at the G2 to M transition
JOURNAL J Cell Biol 156 (2), 249-259 (2002)
PUBMED 11807090
REMARK GeneRIF: checkpoint protein Chfr is a ligase that ubiquitinates
Plk1 and inhibits Cdc2 at the G2 to M transition
REFERENCE 10 (bases 1 to 11228)
AUTHORS Scolnick,D.M. and Halazonetis,T.D.
TITLE Chfr defines a mitotic stress checkpoint that delays entry into
metaphase
JOURNAL Nature 406 (6794), 430-435 (2000)
PUBMED 10935642
COMMENT REVIEWED REFSEQ: This record has been curated by NCBI staff. The
reference sequence was derived from AC127070.10.
This sequence is a reference standard in the RefSeqGene project.
On Aug 2, 2019 this sequence version replaced NM_001161346.1.
Summary: This gene encodes an E3 ubiquitin-protein ligase required
for the maintenance of the antephase checkpoint that regulates cell
cycle entry into mitosis and, therefore, may play a key role in
cell cycle progression and tumorigenesis. The encoded protein has
an N-terminal forkhead-associated domain, a central RING-finger
domain, and a cysteine-rich C-terminal region. Alternatively
spliced transcript variants that encode different protein isoforms
have been described. [provided by RefSeq, Mar 2014].
Sequence Note: The RefSeq transcript and protein were derived from
genomic sequence to make the sequence consistent with the reference
genome assembly. The genomic coordinates used for the transcript
record were based on alignments.
Publication Note: This RefSeq record includes a subset of the
publications that are available for this gene. Please see the Gene
record to access additional publications.
##Evidence-Data-START##
Transcript exon combination :: AK027687.1, SRR11853561.7903.1
[ECO:0000332]
RNAseq introns :: mixed sample support SAMEA1965299,
SAMEA1966682 [ECO:0006172]
##Evidence-Data-END##
##RefSeq-Attributes-START##
MANE Ensembl match :: ENST00000450056.7/ ENSP00000398735.2
RefSeq Select criteria :: based on conservation, expression
##RefSeq-Attributes-END##
COMPLETENESS: complete on the 3' end.
PRIMARY REFSEQ_SPAN PRIMARY_IDENTIFIER PRIMARY_SPAN COMP
1-59 AC127070.10 62213-62271
60-204 AC127070.10 62478-62622
205-304 AC127070.10 72164-72263
305-414 AC127070.10 77424-77533
415-474 AC127070.10 79035-79094
475-654 AC127070.10 80020-80199
655-822 AC127070.10 88184-88351
823-982 AC127070.10 90591-90750
983-1137 AC127070.10 92259-92413
1138-1300 AC127070.10 93188-93350
1301-1443 AC127070.10 96245-96387
1444-1563 AC127070.10 98081-98200
1564-1647 AC127070.10 101094-101177
1648-1718 AC127070.10 101663-101733
1719-1806 AC127070.10 102688-102775
1807-1914 AC127070.10 105684-105791
1915-1987 AC127070.10 106735-106807
1988-11228 AC127070.10 108222-117462
FEATURES Location/Qualifiers
source 1..11228
/organism="Homo sapiens"
/mol_type="mRNA"
/db_xref="taxon:9606"
/chromosome="12"
/map="12q24.33"
gene 1..11228
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/note="checkpoint with forkhead and ring finger domains"
/db_xref="GeneID:55743"
/db_xref="HGNC:HGNC:20455"
/db_xref="MIM:605209"
exon 1..59
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/inference="alignment:Splign:2.1.0"
variation 1
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1951934047"
variation 3
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:534357480"
variation 4
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:570446374"
variation 5
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:896280970"
variation 8
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1951933832"
variation 10
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1452969814"
variation 11
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1468914426"
variation 12
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1951933697"
variation 14
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1951933660"
variation 15..18
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="cagc"
/replace="cagcagc"
/db_xref="dbSNP:1951933544"
variation 16
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1403273314"
variation 17..28
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="gcggcggcg"
/replace="gcggcggcggcg"
/replace="gcggcggcggcggcg"
/db_xref="dbSNP:1462255454"
variation 17
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1052274666"
variation 18
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2137089264"
variation 19
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1023737356"
variation 20
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1951933454"
variation 21
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2137089243"
variation 22
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1177915172"
variation 23
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1305328622"
variation 24
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1043377910"
variation 25
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:942391667"
variation 26
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:910903529"
variation 27..29
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="cgc"
/replace="cgccgc"
/db_xref="dbSNP:1951933091"
variation 27
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:986491943"
variation 28
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1593552393"
variation 29
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1951933065"
variation 30
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:867733545"
variation 31
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:866582582"
variation 32
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1184602056"
variation 33
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1457982394"
variation 34
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1180202481"
variation 35
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1951932815"
variation 36
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:955129324"
variation 37
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1418375663"
variation 39
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:918721775"
variation 40
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1379340094"
variation 41
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:558080896"
variation 42
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1401227842"
variation 45
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1203285887"
variation 46
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1373084089"
variation 47
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1460094658"
variation 48
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1951932409"
variation 49
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:972910573"
variation 50
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:962990830"
variation 51
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1951932291"
variation 53
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2543427215"
variation 55
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1210883392"
variation 56
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1261984726"
variation 57
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1951932164"
variation 58
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1318118652"
variation 59
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1307468722"
exon 60..204
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/inference="alignment:Splign:2.1.0"
variation 62
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1951922592"
misc_feature 63..65
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/note="upstream in-frame stop codon"
variation 63
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1951922549"
variation 64
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:2543424906"
variation 66
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:2543424904"
variation 68..70
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="cc"
/replace="ccc"
/db_xref="dbSNP:1000300479"
variation 68
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:756050840"
variation 69
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1200689283"
variation 70
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:745782659"
variation 71
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1951922329"
CDS 72..2030
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/EC_number="2.3.2.27"
/note="isoform 3 is encoded by transcript variant 3; RING
finger protein 196; checkpoint with forkhead and ring
finger domains, E3 ubiquitin protein ligase; RING-type E3
ubiquitin transferase CHFR"
/codon_start=1
/product="E3 ubiquitin-protein ligase CHFR isoform 3"
/protein_id="NP_001154818.1"
/db_xref="CCDS:CCDS53848.1"
/db_xref="GeneID:55743"
/db_xref="HGNC:HGNC:20455"
/db_xref="MIM:605209"
/translation="
MERPEEGKQSPPPQPWGRLLRLGAEEGEPHVLLRKREWTIGRRRGCDLSFPSNKLVSGDHCRIVVDEKSGQVTLEDTSTSGTVINKLKVVKKQTCPLQTGDVIYLVYRKNEPEHNVAYLYESLSEKQGMTQESFDTSGAGAGRGADPRVPPSSPATQVCFEEPQPSTSTSDLFPTASASSTEPSPAGRERSSSCGSGGGGISPKGSGPSVASDEVSSFASALPDRKTASFSSLEPQDQEDLEPVKKKMRGDGDLDLNGQLLVAQPRRNAQTVHEDVRAAAGKPDKMEETLTCIICQDLLHDCVSLQPCMHTFCAACYSGWMERSSLCPTCRCPVERICKNHILNNLVEAYLIQHPDKSRSEEDVQSMDARNKITQDMLQPKVRRSFSDEEGSSEDLLELSDVDSESSDISQPYVVCRQCPEYRRQAAQPPHCPAPEGEPGAPQALGDAPSTSVSLTTAVQDYVCPLQGSHALCTCCFQPMPDRRAEREQDPRVAPQQCAVCLQPFCHLYWGCTRTGCYGCLAPFCELNLGDKCLDGVLNNNSYESDILKNYLATRGLTWKNMLTESLVALQRGVFLLSDYRVTGDTVLCYCCGLRSFRELTYQYRQNIPASELPVAVTSRPDCYWGRNCRTQVKAHHAMKFNHICEQTRFKN"
misc_feature 72..134
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/note="propagated from UniProtKB/Swiss-Prot (Q96EP1.2);
Region: Disordered. /evidence=ECO:0000256|SAM:MobiDB-lite"
misc_feature 114..443
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/note="forkhead associated (FHA) domain found in
checkpoint with forkhead and RING finger domains protein
(CHFR); Region: FHA_CHFR; cd22672"
/db_xref="CDD:438724"
misc_feature order(114..137,189..191,213..215,219..221,228..230,
234..239,249..254,285..305,309..347,354..365,372..395,
417..443)
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/note="homodimer interface [polypeptide binding]; other
site"
/db_xref="CDD:438724"
misc_feature 162..>794
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/note="Predicted component of the type VI protein
secretion system, contains a FHA domain [Signal
transduction mechanisms, Intracellular trafficking,
secretion, and vesicular transport]; Region: COG3456"
/db_xref="CDD:442679"
misc_feature order(192..200,240..245,249..251,303..314)
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/note="putative phosphopeptide binding site [polypeptide
binding]; other site"
/db_xref="CDD:438724"
misc_feature 765..767
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/note="Phosphoserine.
/evidence=ECO:0007744|PubMed:23186163; propagated from
UniProtKB/Swiss-Prot (Q96EP1.2); phosphorylation site"
misc_feature 927..>1541
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/note="DNA repair protein rad18; Region: rad18; TIGR00599"
/db_xref="CDD:273165"
misc_feature 933..1094
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/note="RING finger, HC subclass, found in checkpoint with
forkhead and RING finger domains protein (CHFR); Region:
RING-HC_CHFR; cd16503"
/db_xref="CDD:438166"
misc_feature 1191..1193
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/note="Phosphothreonine.
/evidence=ECO:0000250|UniProtKB:Q810L3; propagated from
UniProtKB/Swiss-Prot (Q96EP1.2); phosphorylation site"
misc_feature 1197..1286
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/note="propagated from UniProtKB/Swiss-Prot (Q96EP1.2);
Region: Disordered. /evidence=ECO:0000256|SAM:MobiDB-lite"
misc_feature 1350..1418
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/note="propagated from UniProtKB/Swiss-Prot (Q96EP1.2);
Region: Disordered. /evidence=ECO:0000256|SAM:MobiDB-lite"
misc_feature 1425..1895
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/note="Cysteine rich domain with multizinc binding
regions; Region: zf-CRD; pfam17979"
/db_xref="CDD:465602"
misc_feature 1929..2000
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/note="PBZ domain; Region: zf-CCHH; pfam10283"
/db_xref="CDD:463043"
variation 72
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1951922287"
variation 74
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1323042743"
variation 76
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:780919643"
variation 78
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:2543424863"
variation 79
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:757065782"
variation 80
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:879451433"
variation 81
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1252988651"
variation 82
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2543424843"
variation 83
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2543424839"
variation 84
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:2543424835"
variation 85
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:2543424828"
variation 86
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2543424819"
variation 87
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1285867152"
variation 90
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2543424805"
variation 91
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1453369842"
variation 92
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2543424792"
variation 94
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1381686714"
variation 96
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1334460653"
variation 99
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2543424779"
variation 100..111
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="cgccgccgc"
/replace="cgccgccgccgc"
/replace="cgccgccgccgccgc"
/db_xref="dbSNP:765917829"
variation 100
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:752932212"
variation 102
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:372093401"
variation 103
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2543424767"
variation 104
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1566211828"
variation 105
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1459172597"
variation 106
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:2543424751"
variation 107
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:2543424745"
variation 108
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1022133046"
variation 109
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1407689006"
variation 110
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1415407421"
variation 111
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1951921415"
variation 112
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2543424721"
variation 113
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1184750358"
variation 114
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1444571399"
variation 115
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2543424709"
variation 116
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:547086677"
variation 118..121
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="ggg"
/replace="gggg"
/db_xref="dbSNP:1180924768"
variation 118
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1951921231"
variation 120
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:2543424694"
variation 121
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:2543424681"
variation 123
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1481059648"
variation 124
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1951921084"
variation 125
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1593551043"
variation 126
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1951920986"
variation 128
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1327949016"
variation 129
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1250940821"
variation 130
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:2137086568"
variation 131
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:2543424661"
variation 132
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1951920825"
variation 133
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1202757955"
variation 134
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:2543424645"
variation 135
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1323574369"
variation 137
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:2543424636"
variation 138
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1292594475"
variation 140
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1246548917"
variation 141
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2543424629"
variation 142
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1951920619"
variation 143
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:753867941"
variation 144
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1312590714"
variation 145
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2543424617"
variation 146
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1448675201"
variation 148
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1373843772"
variation 149
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:2543424610"
variation 151
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2543424605"
variation 152
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1297235638"
variation 155
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2543424597"
variation 156
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:766461060"
variation 157
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1242357676"
variation 158
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:889736424"
variation 159
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1050716303"
variation 160
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:2543424583"
variation 161
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1163686245"
variation 162
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1424534907"
variation 163..169
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="tcct"
/replace="tcctcct"
/db_xref="dbSNP:2543424553"
variation 164
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:761126986"
variation 165
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:896897715"
variation 166
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:2543424568"
variation 167
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1161017404"
variation 168
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:558346895"
variation 170
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1291046887"
variation 171
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:2543424545"
variation 172
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2543424541"
variation 173
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:994965729"
variation 176
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1250327307"
variation 177
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1951919733"
variation 178
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1037164725"
variation 179
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1175632960"
variation 180
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2543424527"
variation 182..184
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="gtg"
/db_xref="dbSNP:2543424523"
variation 182
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:2137086327"
variation 184..185
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="gg"
/db_xref="dbSNP:2543424521"
variation 185
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1489596045"
variation 186..191
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="accatc"
/db_xref="dbSNP:2543424502"
variation 187
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2543424514"
variation 188
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1269637112"
variation 189
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1329871429"
variation 190
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:2543424504"
variation 191
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="c"
/db_xref="dbSNP:2043630516"
variation 192
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1220935343"
variation 193
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2543424495"
variation 194
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1360131934"
variation 195
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:941122476"
variation 197
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:2543424487"
variation 198
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:2543424485"
variation 199
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1951919358"
variation 200
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2543424480"
variation 201
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1221878184"
variation 202
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1951919241"
exon 205..304
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/inference="alignment:Splign:2.1.0"
variation 206..207
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="t"
/replace="tt"
/db_xref="dbSNP:1566203316"
variation 208
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:762757910"
variation 209
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:775199616"
variation 210
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1016169013"
variation 213
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:370348872"
variation 214..216
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="ttt"
/replace="tttt"
/db_xref="dbSNP:2543406849"
variation 216
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1184762410"
variation 217
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:2543406838"
variation 218
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:2543406835"
variation 219
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:776467669"
variation 221..224
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="ccc"
/replace="cccc"
/db_xref="dbSNP:2137047496"
variation 221
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1371415158"
variation 222
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:765839818"
variation 223
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:770855105"
variation 225
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:146088609"
variation 226
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1951658569"
variation 226
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="gg"
/db_xref="dbSNP:1951658615"
variation 228
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:77052806"
variation 229
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2543406808"
variation 230
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1951658472"
variation 231
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:540426488"
variation 234
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2543406801"
variation 236
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:771849929"
variation 237
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1951658327"
variation 239
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1951658293"
variation 240
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1951658241"
variation 241
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1325393287"
variation 244
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:573017098"
variation 245
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:780255609"
variation 246
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:956973617"
variation 247
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2543406789"
variation 249
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:756177652"
variation 250
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1336502857"
variation 251
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1468386635"
variation 252
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2543406776"
variation 254
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2543406774"
variation 256
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2543406772"
variation 259
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:750466757"
variation 260
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2543406771"
variation 261
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:781107351"
variation 262
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:142824452"
variation 263
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2543406767"
variation 264..267
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="gtgg"
/db_xref="dbSNP:2543406752"
variation 264
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1372280960"
variation 265
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:752104453"
variation 268
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2543406750"
variation 270
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1190933998"
variation 276..286
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="tcaggt"
/replace="tcaggtcaggt"
/db_xref="dbSNP:1951657458"
variation 277
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:2543406746"
variation 278
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1446377947"
variation 279
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:764607751"
variation 280
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2543406738"
variation 283
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:763356188"
variation 285
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2543406731"
variation 287
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2543406726"
variation 289
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1436266778"
variation 290
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:115711908"
variation 291
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1252203966"
variation 293
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1951657255"
variation 294
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:2543406709"
variation 296
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1390531305"
variation 301
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1196075617"
variation 302
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:764905392"
variation 303
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:2543406694"
variation 304
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:996565819"
exon 305..414
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/inference="alignment:Splign:2.1.0"
variation 305
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2543398237"
variation 307
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1405603798"
variation 308
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:200283117"
variation 311
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1951510439"
variation 312
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2543398225"
variation 313
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1951510403"
variation 314
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2543398217"
variation 317
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:138320999"
variation 318
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2543398211"
variation 320
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1262248032"
variation 322
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2543398203"
variation 326
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:2543398200"
variation 328
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1403538188"
variation 329
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1593510822"
variation 335
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:2543398192"
variation 336..341
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="gtt"
/replace="gttgtt"
/db_xref="dbSNP:749471534"
variation 338
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1026698840"
variation 339
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2543398183"
variation 340
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2543398181"
variation 341
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:2543398178"
variation 343
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1951510106"
variation 345
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:753427887"
variation 347
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1409273260"
variation 348
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:765931951"
variation 349
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:145622325"
variation 350
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:896801495"
variation 353
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1951509886"
variation 354
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2543398161"
variation 356
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2543398157"
variation 357
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1220821081"
variation 358
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1951509767"
variation 361
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2543398147"
variation 362
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1951509715"
variation 364
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:773164146"
variation 366
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:1285340068"
variation 369
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2543398140"
variation 370
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:2543398137"
variation 375
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1593510705"
variation 377
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:2543398133"
variation 378
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1204882792"
variation 382
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1349041006"
variation 384
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:767392115"
variation 386
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:761633567"
variation 387
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:774239471"
variation 388
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2543398120"
variation 391
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:2543398118"
variation 392
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:768330210"
variation 394
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1951509269"
variation 395
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2543398108"
variation 397
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2543398102"
variation 398
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2543398098"
variation 400
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1281470229"
variation 402
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1036686943"
variation 404
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1277101257"
variation 406
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:377703818"
variation 407
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:771143796"
variation 411
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:201058448"
variation 412
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:778449705"
variation 413
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="c"
/db_xref="dbSNP:2543398074"
variation 413
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1951508921"
variation 414
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:758996497"
exon 415..474
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/inference="alignment:Splign:2.1.0"
variation 415
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2543395291"
variation 416
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:368692761"
variation 417
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:765096474"
variation 419
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2543395281"
variation 420
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1300704622"
variation 422
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:761045629"
variation 423
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1402185439"
variation 424
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:2543395264"
variation 426
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:773555344"
variation 427
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:2543395260"
variation 428
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:2543395256"
variation 429..431
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="t"
/replace="tat"
/db_xref="dbSNP:2543395249"
variation 429
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1951471364"
variation 430
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:772208422"
variation 433
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2543395245"
variation 435
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:2543395241"
variation 437..439
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="ttt"
/replace="tttt"
/db_xref="dbSNP:2137020043"
variation 438
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1428337510"
variation 439
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2543395236"
variation 440
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:2543395232"
variation 441
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1387598301"
variation 442
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1951471200"
variation 447..453
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="aag"
/replace="aagcaag"
/db_xref="dbSNP:2543395221"
variation 448
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2543395224"
variation 449
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1164831443"
variation 453
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:202105666"
variation 454
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:769092725"
variation 456
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1415955003"
variation 459
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1312795252"
variation 461
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:374502930"
variation 462
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:761297928"
variation 463
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1481092256"
variation 465
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:780460479"
variation 467
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:773617187"
variation 470
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1443614623"
variation 471
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:2543395191"
variation 473
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1951470668"
exon 475..654
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/inference="alignment:Splign:2.1.0"
variation 475..482
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="atacctca"
/replace="atacctcatacctca"
/db_xref="dbSNP:2543393349"
variation 475
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:1415698891"
variation 476..478
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="tac"
/replace="tactac"
/db_xref="dbSNP:2543393355"
variation 477
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2543393357"
variation 478..481
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="cctc"
/db_xref="dbSNP:1951442868"
variation 478
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1951442959"
variation 480
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:1951442927"
variation 481..496
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="caggtgcagg"
/replace="caggtgcaggtgcagg"
/replace="caggtgcaggtgcaggtgcagg"
/db_xref="dbSNP:1566196191"
variation 482
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1951442837"
variation 484
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2543393344"
variation 485
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1345035376"
variation 486
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2543393341"
variation 489
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:529705996"
variation 490
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:968187911"
variation 491
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1053846225"
variation 496..497
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="tgcagt"
/db_xref="dbSNP:1951442404"
variation 496
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1430015478"
variation 497
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1566196184"
variation 498
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2543393312"
variation 499
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:761341813"
variation 501..504
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="gggg"
/replace="ggggg"
/db_xref="dbSNP:1431549533"
variation 501
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:2543393305"
variation 504
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:2543393301"
variation 506
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1265155365"
variation 507
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:768775618"
variation 510
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:565366267"
variation 511
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1267263973"
variation 512
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:547367271"
variation 513
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:746187833"
variation 514
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:780923793"
variation 515
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1951441836"
variation 516
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1951441794"
variation 518
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2543393280"
variation 520
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1231852845"
variation 521
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1309985498"
variation 523
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1298364440"
variation 524
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1951441603"
variation 525
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1951441554"
variation 526
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1030329804"
variation 527
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:199790262"
variation 528
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1318983295"
variation 529
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:371470066"
variation 530
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:777219646"
variation 532
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1176037831"
variation 533
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1422710949"
variation 534
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:998173223"
variation 535
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1951441033"
variation 537
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1359228046"
variation 538
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:757969077"
variation 540
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:748110156"
variation 541
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1951440849"
variation 542
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:991093892"
variation 543
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:775208965"
variation 545
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1186481589"
variation 547
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1462519990"
variation 548
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1951440598"
variation 549
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:2543393223"
variation 551
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:2543393221"
variation 552..554
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="gag"
/replace="gagag"
/db_xref="dbSNP:2543393214"
variation 553
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:2543393219"
variation 558
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2543393212"
variation 559
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1951440531"
variation 560
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1212965676"
variation 561
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1243354590"
variation 562
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:756710137"
variation 564
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1951440329"
variation 565
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1951440283"
variation 568
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1951440243"
variation 569
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1951440193"
variation 570
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2543393183"
variation 571
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:959491929"
variation 572
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:753235007"
variation 574
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:778929950"
variation 575
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:909400005"
variation 576
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:2543393168"
variation 577
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1252563891"
variation 578
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:754853631"
variation 580
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2543393162"
variation 585
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1342113004"
variation 590
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1296093228"
variation 591
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:368788828"
variation 593
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2543393152"
variation 594
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1398898916"
variation 595
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1951439655"
variation 598
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:984493040"
variation 599
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2543393144"
variation 601
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1048846757"
variation 602
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:528825047"
variation 603
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:564810555"
variation 604
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1382340206"
variation 608
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:751789347"
variation 609
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1298843354"
variation 610
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:546136386"
variation 611
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1430290279"
variation 612
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:2543393117"
variation 613
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:541715629"
variation 614
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:75391939"
variation 615
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1593503337"
variation 616
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1166700448"
variation 617
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1951438999"
variation 618
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2543393101"
variation 619
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:2543393097"
variation 620
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1446218228"
variation 622..626
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="ct"
/replace="ctcct"
/db_xref="dbSNP:1593503293"
variation 623
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:2543393088"
variation 624
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1385634222"
variation 625
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:2543393083"
variation 627
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1951438819"
variation 628
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2543393076"
variation 629
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:965751134"
variation 630
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:2543393072"
variation 632
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:563840755"
variation 633
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:745321936"
variation 634
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:776005190"
variation 638
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2543393056"
variation 639
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1042155534"
variation 640
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:765687815"
variation 641
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2543393046"
variation 643
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:2543393042"
variation 644
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:2543393040"
variation 645
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:1460603946"
variation 646
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1951438339"
variation 647
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:2543393033"
variation 648
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1381533831"
variation 649
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:2543393030"
variation 652
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1225450271"
exon 655..822
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/inference="alignment:Splign:2.1.0"
variation 655
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:2543364670"
variation 658
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1038150337"
variation 660..664
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="ggggg"
/replace="gggggg"
/db_xref="dbSNP:2543364624"
variation 660
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:370517411"
variation 661
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1951211639"
variation 663
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1438318944"
variation 664
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:777186106"
variation 665
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:2543364593"
variation 666..667
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="gg"
/db_xref="dbSNP:1189456093"
variation 666
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:766667278"
variation 668
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2543364550"
variation 669
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:761034338"
variation 670
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1593482765"
variation 672
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:138637226"
variation 674
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1951211154"
variation 675
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1387477118"
variation 676
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2543364484"
variation 677
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2543364472"
variation 678
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:34220055"
variation 679
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:761525824"
variation 680
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2136982888"
variation 684
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:2543364419"
variation 685
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1951210868"
variation 688..692
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="gtggt"
/replace="gtggtggt"
/db_xref="dbSNP:2543364376"
variation 688
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:774070010"
variation 689
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1419993206"
variation 690
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1951210693"
variation 691
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:201192149"
variation 692
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:989203291"
variation 694
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1951210512"
variation 695
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2543364365"
variation 696
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2543364361"
variation 697
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2543364355"
variation 698
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:796201985"
variation 699
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1163339779"
variation 706
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2543364338"
variation 707
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:749192848"
variation 708
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2543364322"
variation 710
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2543364318"
variation 711
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:374107669"
variation 713
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:769505625"
variation 716..730
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="ctc"
/replace="ctccagctttgcctc"
/db_xref="dbSNP:2543364248"
variation 716..719
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="ctcc"
/db_xref="dbSNP:2543364278"
variation 716
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2543364296"
variation 718
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:780945230"
variation 719
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2543364271"
variation 721
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2543364264"
variation 722
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1951210091"
variation 730
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2543364239"
variation 731
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1951210040"
variation 734
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2543364222"
variation 735
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:35206714"
variation 737
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1951209926"
variation 738
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1366834805"
variation 739
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2543364205"
variation 740
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1038008124"
variation 742
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:560433355"
variation 744..750
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="aga"
/replace="agaaaga"
/db_xref="dbSNP:1951209560"
variation 746
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2543364172"
variation 747
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:201727566"
variation 751
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:2136982730"
variation 752
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:758662673"
variation 753
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:533118486"
variation 754
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:150995074"
variation 755
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:755027328"
variation 756..760
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="t"
/replace="tcctt"
/db_xref="dbSNP:2136982677"
variation 758
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:908433616"
variation 761
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:200213031"
variation 763
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:754307363"
variation 764
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:145246258"
variation 766
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:141183005"
variation 767
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:767988129"
variation 768..769
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="t"
/replace="tt"
/db_xref="dbSNP:766718829"
variation 768
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2543364036"
variation 769
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2543364017"
variation 770
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1566189184"
variation 771
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1423637297"
variation 774..777
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="ccc"
/replace="cccc"
/db_xref="dbSNP:762524769"
variation 774
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:751592981"
variation 776
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1951208832"
variation 778
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:373754363"
variation 779
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:761615752"
variation 780
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:147803776"
variation 782
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1566189143"
variation 784
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1951208615"
variation 785
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:2543363936"
variation 786
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2543363927"
variation 788
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:774088595"
variation 789
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1472958431"
variation 792
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2543363887"
variation 797
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:768052255"
variation 798..800
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="cc"
/replace="ccc"
/db_xref="dbSNP:2136982524"
variation 798
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:2543363872"
variation 799
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:762481129"
variation 800
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1025589682"
variation 801
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:775309126"
variation 803
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:764279540"
variation 804
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1951208249"
variation 805
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1463671908"
variation 807
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:974854406"
variation 809
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:2543363800"
variation 810
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1221100387"
variation 811
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1951208117"
variation 812
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:1238379063"
variation 813
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1951208036"
variation 814
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1566189061"
variation 815
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2543363750"
variation 819
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:745763828"
variation 820
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:2543363733"
exon 823..982
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/inference="alignment:Splign:2.1.0"
variation 823
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1951157533"
variation 824
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:756088633"
variation 827
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1951157390"
variation 828
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:563202190"
variation 831
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:2136974267"
variation 832
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1360404336"
variation 833
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2543354199"
variation 835
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1951157150"
variation 836
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:781748631"
variation 837
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2543354173"
variation 838
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2543354169"
variation 839
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:757715316"
variation 840
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2543354149"
variation 841
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:752016583"
variation 842
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:377318460"
variation 843
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:115096950"
variation 844
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1593477819"
variation 845
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1393923793"
variation 846..847
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="t"
/db_xref="dbSNP:776753889"
variation 847
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:1311480210"
variation 848
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:758139441"
variation 849
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:973250523"
variation 851
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1021390710"
variation 855
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:752281100"
variation 857
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:115431373"
variation 858
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:148618944"
variation 859
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2543353949"
variation 860
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:369526598"
variation 863
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:769878915"
variation 864
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:540759128"
variation 865
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:760584451"
variation 866
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:773102049"
variation 867
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:749537035"
variation 868
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:375174098"
variation 870
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="aa"
/db_xref="dbSNP:2543353872"
variation 870
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:770024903"
variation 872
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:2543353859"
variation 873
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1951155348"
variation 874
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:2543353847"
variation 876
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:188170704"
variation 877
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:745889598"
variation 878
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1951155139"
variation 879
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:781395404"
variation 881
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:757876886"
variation 882
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1593477690"
variation 883
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1951154950"
variation 884
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:747517165"
variation 885
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:199761208"
variation 888
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1951154859"
variation 890
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1380131918"
variation 891
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:144838296"
variation 893
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1449844658"
variation 895
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1000960906"
variation 896
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:371434249"
variation 897
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:764757412"
variation 898
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="t"
/db_xref="dbSNP:768680290"
variation 898
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1464052810"
variation 900
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:754506935"
variation 901
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:149862277"
variation 903
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2543353724"
variation 904
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2136973920"
variation 905
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:765845584"
variation 907
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1277312621"
variation 908
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:746414469"
variation 909
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1341883561"
variation 910
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:2136973888"
variation 911
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1295926976"
variation 912
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2543353667"
variation 913
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1306779303"
variation 915
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1593477559"
variation 916
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1375950961"
variation 917
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:2543353625"
variation 918
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:2543353610"
variation 919
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2136973857"
variation 920
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:35011845"
variation 921
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1341253353"
variation 923
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1951153923"
variation 924
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2543353510"
variation 926
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1312306793"
variation 927
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:767348322"
variation 928
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2543353481"
variation 929
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1352413194"
variation 932
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2136973793"
variation 935
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:2136973786"
variation 937
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:761474515"
variation 938
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:775799321"
variation 939
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2136973760"
variation 940
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:2543353424"
variation 941
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1951153687"
variation 942
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1951153632"
variation 943
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:2543353402"
variation 944
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1369689338"
variation 946
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2136973741"
variation 948
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1951153534"
variation 950
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:770185579"
variation 951
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1252007101"
variation 953
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:12315353"
variation 954
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:2543353342"
variation 955
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:2543353332"
variation 956
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:146107503"
variation 958
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2543353313"
variation 962
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1368629651"
variation 965
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1186411942"
variation 966..977
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="ctgcacgactgc"
/replace="ctgcacgactgcacgactgc"
/db_xref="dbSNP:2543353240"
variation 966
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1951153233"
variation 967
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:759798633"
variation 968
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:2136973671"
variation 969
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1951153155"
variation 971
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1253421391"
variation 972
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1951153058"
variation 974
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:2543353253"
variation 975
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2543353246"
variation 977
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:776915637"
variation 978
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="g"
/db_xref="dbSNP:2543353225"
variation 978
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:771123706"
variation 980
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1469130916"
variation 981
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2543353205"
exon 983..1137
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/inference="alignment:Splign:2.1.0"
variation 983
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:560066373"
variation 987
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1213141444"
variation 990
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2543345061"
variation 991
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:780721649"
variation 992
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:565644778"
variation 996
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:987211916"
variation 999
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1566185781"
variation 1000
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1174814592"
variation 1001
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1478670195"
variation 1002
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2543345020"
variation 1003
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:751498855"
variation 1004
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:142975525"
variation 1007
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1466544467"
variation 1008
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2543344987"
variation 1010
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:138280939"
variation 1011
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:754144763"
variation 1012
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:921635691"
variation 1013
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:766660009"
variation 1014
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:760933260"
variation 1015
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1221124973"
variation 1018
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:2543344929"
variation 1021
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:368405665"
variation 1022
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:767634272"
variation 1024
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:762287710"
variation 1025
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1367099211"
variation 1026
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2543344893"
variation 1027
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:774770261"
variation 1028
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1951109519"
variation 1030
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2543344874"
variation 1032
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1433978124"
variation 1034
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:553735979"
variation 1036
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:968563777"
variation 1038
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:749601873"
variation 1039
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:775805064"
variation 1042
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1402056016"
variation 1043
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:769371058"
variation 1044
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1593473549"
variation 1046
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:745529097"
variation 1047..1048
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="ct"
/db_xref="dbSNP:1951108714"
variation 1047
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2543344762"
variation 1048
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:2543344746"
variation 1050
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1951108652"
variation 1051
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2543344729"
variation 1052
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:780623191"
variation 1055
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:2543344698"
variation 1056
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:535313174"
variation 1057
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:756736276"
variation 1059
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1474574138"
variation 1061
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2543344650"
variation 1062
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:770034782"
variation 1063
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:146343801"
variation 1064
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2543344627"
variation 1065
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2543344621"
variation 1066
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1441931198"
variation 1068
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:571101753"
variation 1069
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:2543344593"
variation 1070
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:115029653"
variation 1071
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1344021759"
variation 1073
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2543344552"
variation 1076
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2543344541"
variation 1077
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:182092641"
variation 1078
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:756361707"
variation 1081
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:2543344517"
variation 1082
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1359376881"
variation 1084
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:141404869"
variation 1086
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1951107709"
variation 1087
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:767497782"
variation 1089
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1313496770"
variation 1090
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1319716667"
variation 1091
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1339366523"
variation 1093
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1951107360"
variation 1094
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1951107293"
variation 1097
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:375199215"
variation 1100
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:2543344426"
variation 1101
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:2543344414"
variation 1102
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:774858017"
variation 1103
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1951107092"
variation 1104
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1371529354"
variation 1105
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:764629991"
variation 1106
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:2543344348"
variation 1107
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1255988921"
variation 1109
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:191062458"
variation 1110
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:775898959"
variation 1113
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1182669640"
variation 1114
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2543344289"
variation 1116
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1213131732"
variation 1117
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1241168194"
variation 1118
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:2543344223"
variation 1120
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1593473382"
variation 1121
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:148311652"
variation 1124
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:143181439"
variation 1125
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1241159400"
variation 1126
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1593473335"
variation 1127
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:770380694"
variation 1129
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:2543344140"
variation 1131
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:746470663"
variation 1132
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:370386571"
variation 1133
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2136966487"
variation 1134
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2543344087"
variation 1135
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1951106171"
exon 1138..1300
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/inference="alignment:Splign:2.1.0"
variation 1139
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1227736511"
variation 1140..1141
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="aa"
/db_xref="dbSNP:777961507"
variation 1140
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:2543338742"
variation 1144..1147
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="gtcg"
/replace="gtcgtcg"
/db_xref="dbSNP:2543338691"
variation 1144
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:2543338713"
variation 1146
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1210874026"
variation 1147
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:2543338682"
variation 1148
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:928539042"
variation 1152..1159
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="gaaga"
/replace="gaagaaga"
/db_xref="dbSNP:1951075030"
variation 1152
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1951075098"
variation 1154
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1566184554"
variation 1161
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:879123151"
variation 1162
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:2543338640"
variation 1163
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1229649968"
variation 1164
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:2543338608"
variation 1165
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:777930523"
variation 1166
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1566184534"
variation 1168
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1293723698"
variation 1170
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:377225060"
variation 1174
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:748309050"
variation 1175
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:778828908"
variation 1176
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1434082116"
variation 1177
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:200764395"
variation 1178
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:369063253"
variation 1179
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:1026572995"
variation 1180
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:766865645"
variation 1181
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:2062163"
variation 1188
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2543338442"
variation 1189
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1047280041"
variation 1190
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:750119581"
variation 1191
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2543338420"
variation 1192
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:760238279"
variation 1194
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:761337268"
variation 1198
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2543338402"
variation 1200
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:150467142"
variation 1204
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:2543338381"
variation 1206
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2543338378"
variation 1207
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2543338376"
variation 1208
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:763498728"
variation 1209
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2543338359"
variation 1210
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2543338353"
variation 1212
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1951074170"
variation 1217
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:930183182"
variation 1218
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1322357484"
variation 1219
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:762961678"
variation 1220
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:879252133"
variation 1221
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:920205326"
variation 1222
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:201828860"
variation 1223
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2543338319"
variation 1224
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1593470536"
variation 1225
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:769607729"
variation 1226
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:745615761"
variation 1229
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:776390811"
variation 1231
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2543338293"
variation 1233
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:974463026"
variation 1235
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:2543338283"
variation 1236..1242
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="gaag"
/replace="gaagaag"
/db_xref="dbSNP:1434190222"
variation 1241
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:2543338280"
variation 1243
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:772321674"
variation 1246
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1315657949"
variation 1249
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="cc"
/db_xref="dbSNP:1951073572"
variation 1249
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1413044699"
variation 1250
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2543338254"
variation 1253
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1353432969"
variation 1257
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1951073448"
variation 1260
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1309789349"
variation 1262
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2543338209"
variation 1263
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2543338206"
variation 1265
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:748314312"
variation 1271
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="aa"
/db_xref="dbSNP:2543338195"
variation 1271
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1283784330"
variation 1272
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1951073286"
variation 1274
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1395585538"
variation 1275
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1165776578"
variation 1281
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1951073172"
variation 1282
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2543338155"
variation 1283
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1951073138"
variation 1284
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2543338148"
variation 1285
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:779111370"
variation 1286
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1951073053"
variation 1289
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1368718436"
variation 1291
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1951072973"
variation 1295
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2543338118"
variation 1298
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:754958760"
variation 1299
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="a"
/db_xref="dbSNP:2543338100"
exon 1301..1443
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/inference="alignment:Splign:2.1.0"
variation 1301
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2543324234"
variation 1302
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2543324220"
variation 1304
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1286314037"
variation 1305
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1020597739"
variation 1307
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:748419509"
variation 1308
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:372270460"
variation 1309
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="aa"
/db_xref="dbSNP:2543324171"
variation 1309
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1013270057"
variation 1310
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1438322046"
variation 1311
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:768814594"
variation 1312
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1318363216"
variation 1313
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:749373830"
variation 1314
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:150627547"
variation 1316
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:368755833"
variation 1318
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2543324120"
variation 1319
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2543324116"
variation 1320
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1435723841"
variation 1321
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:746360566"
variation 1322
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1191956640"
variation 1324
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:2543324077"
variation 1328
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1451601823"
variation 1330
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:781699438"
variation 1331
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2543324059"
variation 1333
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:757496767"
variation 1334
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2543324051"
variation 1337
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1192492326"
variation 1338
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2543324037"
variation 1339
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950995102"
variation 1341
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1445358565"
variation 1342
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950994995"
variation 1344
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2543324010"
variation 1347
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2543324005"
variation 1348
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:374229656"
variation 1349
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:777240371"
variation 1350
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1303770543"
variation 1351
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:371541325"
variation 1352
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:563852229"
variation 1356
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1231849613"
variation 1357
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1950994654"
variation 1358
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2543323920"
variation 1359..1362
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="ccc"
/replace="cccc"
/db_xref="dbSNP:2543323875"
variation 1359
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1366854652"
variation 1360
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1270421677"
variation 1361
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1429332642"
variation 1362
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:2543323862"
variation 1363
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1176161885"
variation 1364
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:764723102"
variation 1367
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:2543323834"
variation 1370
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2136951422"
variation 1371
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2543323815"
variation 1372
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:2543323804"
variation 1373
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:2543323795"
variation 1374
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1237028076"
variation 1376
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:759529335"
variation 1377
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:753721064"
variation 1379
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1375184437"
variation 1380
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1950993996"
variation 1381
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:367968934"
variation 1382
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:374006779"
variation 1383
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:774658371"
variation 1384
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1167629443"
variation 1385
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1566181842"
variation 1386
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:924051400"
variation 1387
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1593463729"
variation 1388
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1041545091"
variation 1389
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2543323672"
variation 1392
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:768798394"
variation 1393..1396
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="ccc"
/replace="cccc"
/db_xref="dbSNP:2543323625"
variation 1394
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1239336733"
variation 1398
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:2543323616"
variation 1399
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1950993248"
variation 1401
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2543323587"
variation 1403
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:2543323578"
variation 1405
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:2543323565"
variation 1406..1410
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="gggg"
/replace="ggggg"
/db_xref="dbSNP:2543323517"
variation 1407
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950993189"
variation 1409
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1189940191"
variation 1410
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2543323506"
variation 1411
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:2543323497"
variation 1412
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1950993053"
variation 1413
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2543323464"
variation 1414
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:138207644"
variation 1415
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1593463695"
variation 1416
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1256747525"
variation 1417
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:2543323408"
variation 1418
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1379314322"
variation 1419
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:775767314"
variation 1422
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1196421815"
variation 1423
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:769933100"
variation 1424
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:746380972"
variation 1425
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:1215461680"
variation 1427
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:781511228"
variation 1428
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:141835819"
variation 1430
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:2543323304"
variation 1431
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2543323293"
variation 1432
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:747380214"
variation 1433
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:2543323273"
variation 1435
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:778169456"
variation 1437
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1355326421"
variation 1438
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="c"
/db_xref="dbSNP:2543323253"
variation 1438
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:752333209"
variation 1439
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:536396076"
variation 1441
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:2543323215"
exon 1444..1563
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/inference="alignment:Splign:2.1.0"
variation 1444
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1402157616"
variation 1445
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:757077660"
variation 1446
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1950950768"
variation 1448
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:146976267"
variation 1450
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:765605647"
variation 1451
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1408464611"
variation 1453
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2543314607"
variation 1455
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2136945225"
variation 1457
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:141349945"
variation 1458
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:776642806"
variation 1462
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1593459784"
variation 1463
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1306934237"
variation 1464
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:764423128"
variation 1465
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1950950185"
variation 1467
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:766469365"
variation 1469
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:761102171"
variation 1470
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2136945164"
variation 1472
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2543314555"
variation 1474
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1304421220"
variation 1478
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:773703522"
variation 1479
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:772460210"
variation 1481
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:147791929"
variation 1482
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1454391193"
variation 1485
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2543314519"
variation 1486
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1345653105"
variation 1487
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:116286061"
variation 1488
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2543314500"
variation 1490
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:768361418"
variation 1491
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1593459724"
variation 1492
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1396714833"
variation 1493..1500
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="ctgct"
/replace="ctgctgct"
/db_xref="dbSNP:1363396811"
variation 1493
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:748952886"
variation 1494
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:763257394"
variation 1496
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1278317795"
variation 1500
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2543314453"
variation 1502
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1950949058"
variation 1503
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1593459675"
variation 1504
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:779441212"
variation 1505
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:775978433"
variation 1508
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2543314418"
variation 1509
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:2543314409"
variation 1511
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:2543314404"
variation 1512
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1187706335"
variation 1514
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:781224248"
variation 1515
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:757239007"
variation 1516
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1593459653"
variation 1518
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:936864653"
variation 1519
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:969442993"
variation 1520
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:2543314352"
variation 1521
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:2543314348"
variation 1522
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:751440176"
variation 1524
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1950948312"
variation 1525
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2306541"
variation 1526..1527
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="gg"
/replace="ggg"
/db_xref="dbSNP:2543314313"
variation 1526
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:755310429"
variation 1527
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1298012137"
variation 1529
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950947947"
variation 1530
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:754035414"
variation 1531
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:944300584"
variation 1532
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:766376169"
variation 1533
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:150920425"
variation 1536
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1015010652"
variation 1537
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:773617183"
variation 1539
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950947517"
variation 1541
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2136944907"
variation 1543
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:768065335"
variation 1544
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:142511371"
variation 1545
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:114117795"
variation 1546..1549
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="gt"
/replace="gtgt"
/db_xref="dbSNP:1950947070"
variation 1546
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:201454195"
variation 1547
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1172173801"
variation 1548
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:200436687"
variation 1550..1555
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="cgcccc"
/db_xref="dbSNP:2543314175"
variation 1550
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:920038038"
variation 1551
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:746554223"
variation 1553
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:973207321"
variation 1557
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1486915053"
variation 1559
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1346472721"
variation 1560
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1258850426"
variation 1561
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2543314164"
variation 1562
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:769207559"
variation 1563
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:2543314150"
exon 1564..1647
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/inference="alignment:Splign:2.1.0"
variation 1566
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:372012714"
variation 1567
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:201350082"
variation 1568
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:7975454"
variation 1571
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:375656978"
variation 1572
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2543298870"
variation 1575
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2543298866"
variation 1577
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1335016856"
variation 1578
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2543298855"
variation 1579
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:201237898"
variation 1580
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1442703181"
variation 1581..1582
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="cc"
/db_xref="dbSNP:2543298823"
variation 1581
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:765505226"
variation 1582
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1324580295"
variation 1583..1585
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="ttt"
/replace="tttt"
/db_xref="dbSNP:2543298814"
variation 1585
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2543298809"
variation 1586
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950877727"
variation 1588
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950877687"
variation 1589
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950877658"
variation 1591
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1403110794"
variation 1592
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:2543298788"
variation 1598
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:759242088"
variation 1599
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:2543298779"
variation 1600..1603
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="ggg"
/replace="gggg"
/db_xref="dbSNP:1950877531"
variation 1601
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:2543298775"
variation 1603
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:953787024"
variation 1607
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:546055046"
variation 1608
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1593453012"
variation 1609
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:766020195"
variation 1611
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:371092913"
variation 1612
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:146156998"
variation 1613
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1454840670"
variation 1614
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:979112170"
variation 1615
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1252629926"
variation 1616
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:772089817"
variation 1617
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1448818469"
variation 1619
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1593452935"
variation 1620
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1950876982"
variation 1621
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:2543298675"
variation 1622
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1249069969"
variation 1623
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2543298661"
variation 1624
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:767140702"
variation 1625
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:765611625"
variation 1626
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1349644861"
variation 1627
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2543298627"
variation 1631
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:189987561"
variation 1632
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1236250946"
variation 1634
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:966632867"
variation 1635
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:2543298606"
variation 1637
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950876673"
variation 1638
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1348083185"
variation 1639
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1302248351"
variation 1640
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1433674477"
variation 1643
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1327743680"
exon 1648..1718
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/inference="alignment:Splign:2.1.0"
variation 1648
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2543295705"
variation 1649
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:777921940"
variation 1652..1653
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="ca"
/replace="caca"
/db_xref="dbSNP:2543295692"
variation 1652
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="cgccatcacagtccatcac"
/db_xref="dbSNP:2543295695"
variation 1653
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:2543295687"
variation 1654
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1950866672"
variation 1655
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:200853567"
variation 1656
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2543295665"
variation 1657
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:2543295654"
variation 1658
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:748721756"
variation 1659
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1179840200"
variation 1661
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950866525"
variation 1662
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950866486"
variation 1663
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:2543295611"
variation 1664
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1471040037"
variation 1665
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1950866384"
variation 1666
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2543295575"
variation 1667
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1415191475"
variation 1669
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1233090445"
variation 1671
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2543295547"
variation 1676
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:372404283"
variation 1677
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:755522022"
variation 1678
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:754297675"
variation 1679
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1323808548"
variation 1680
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2543295514"
variation 1686..1695
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="aacaaca"
/replace="aacaacaaca"
/db_xref="dbSNP:1950865942"
variation 1686
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:2543295506"
variation 1687
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2543295502"
variation 1688
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1213796881"
variation 1689
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:780565079"
variation 1690
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1288355908"
variation 1692..1693
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="aa"
/replace="aaa"
/db_xref="dbSNP:2543295471"
variation 1693
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1225827826"
variation 1694
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:755891788"
variation 1696
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1288380542"
variation 1700
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:749973618"
variation 1701
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950865817"
variation 1702
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:1379904886"
variation 1703
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:767082498"
variation 1707
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1950865707"
variation 1708
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:1950865670"
variation 1709
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1416698488"
variation 1710
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2543295374"
variation 1712
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2543295362"
variation 1713
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:761176081"
variation 1716
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:2543295342"
variation 1718
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1326600805"
exon 1719..1806
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/inference="alignment:Splign:2.1.0"
variation 1719
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2543288794"
variation 1720
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1432073088"
variation 1721
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950847784"
variation 1724
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1422500887"
variation 1725
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:899072283"
variation 1726
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1008556440"
variation 1729
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950847611"
variation 1731
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:776466473"
variation 1733
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1950847509"
variation 1735
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:576074865"
variation 1737..1748
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="gg"
/replace="ggtttgacatgg"
/db_xref="dbSNP:1950847213"
variation 1737
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:2543288713"
variation 1738
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:2543288687"
variation 1739
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:2543288674"
variation 1740
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:2306537"
variation 1745
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:536151635"
variation 1746
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1281285798"
variation 1747
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1378971375"
variation 1749..1753
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="aaaa"
/replace="aaaaa"
/replace="aaaaaa"
/db_xref="dbSNP:1224656808"
variation 1753
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1232869629"
variation 1754
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2543288535"
variation 1755
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:200187965"
variation 1758
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2543288518"
variation 1760
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:2543288509"
variation 1761
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:2136929281"
variation 1762..1763
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="cc"
/replace="ccc"
/db_xref="dbSNP:2543288489"
variation 1763
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:749821203"
variation 1764
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:780655269"
variation 1770
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:770399858"
variation 1772
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:899313894"
variation 1773
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:2306536"
variation 1776
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1485801990"
variation 1777
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:781614371"
variation 1778
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:756917083"
variation 1779
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:2543288393"
variation 1781
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950846511"
variation 1782
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2543288381"
variation 1783
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1313082363"
variation 1784
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1465200907"
variation 1785
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1357095646"
variation 1786
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:558156375"
variation 1789
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:2543288351"
variation 1793
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1363290036"
variation 1796
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:2543288344"
variation 1797
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="c"
/db_xref="dbSNP:1428595949"
variation 1797
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2543288329"
variation 1799
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2543288322"
variation 1802
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2543288317"
variation 1804
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1423530802"
variation 1806
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1950846204"
exon 1807..1914
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/inference="alignment:Splign:2.1.0"
variation 1807
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1265969471"
variation 1811
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950758429"
variation 1812..1815
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="ag"
/replace="agag"
/db_xref="dbSNP:1950758380"
variation 1813
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:2543275608"
variation 1814
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:2543275605"
variation 1815
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2543275594"
variation 1816
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:2543275584"
variation 1819
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:115684143"
variation 1820
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1222086097"
variation 1821
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950758289"
variation 1828
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2543275553"
variation 1829
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:115566777"
variation 1830
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:758025460"
variation 1832
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:976650599"
variation 1833
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:747697880"
variation 1834
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:1566173893"
variation 1835
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:2543275512"
variation 1837
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1950757987"
variation 1838
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2543275506"
variation 1840
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="aa"
/db_xref="dbSNP:2136917535"
variation 1840
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1356919481"
variation 1841
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2543275494"
variation 1842
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:778392987"
variation 1843
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:754931883"
variation 1844
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1442480016"
variation 1846
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2543275462"
variation 1849
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2543275457"
variation 1853
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:937547511"
variation 1854
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:961309862"
variation 1855
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:557461509"
variation 1856
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1456695524"
variation 1858
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:766096241"
variation 1859
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:2136917474"
variation 1863
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:376798546"
variation 1864
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950757414"
variation 1865
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2543275394"
variation 1868
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950757365"
variation 1869
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1439266364"
variation 1871
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2543275383"
variation 1873
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:764448295"
variation 1874
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950757240"
variation 1875
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1220708351"
variation 1876
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:2543275358"
variation 1877
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1195509679"
variation 1878
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:2136917397"
variation 1879
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:114483951"
variation 1880
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1950757063"
variation 1882
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2543275326"
variation 1883
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2543275320"
variation 1884
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:775769340"
variation 1885
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:144644143"
variation 1891
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950756927"
variation 1892
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1950756882"
variation 1896
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:2543275301"
variation 1897
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2543275299"
variation 1904
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:373411620"
variation 1905
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:777155485"
variation 1911
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:76224039"
variation 1913
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2543275274"
variation 1914
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:2543275269"
exon 1915..1987
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/inference="alignment:Splign:2.1.0"
variation 1915
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="t"
/replace="tt"
/db_xref="dbSNP:2543271170"
variation 1917
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2543271165"
variation 1918
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2543271163"
variation 1919
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:772354359"
variation 1920
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:761464761"
variation 1921
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2543271137"
variation 1921
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="t"
/replace="tt"
/db_xref="dbSNP:1476434657"
variation 1923
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1425682767"
variation 1926
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1593440414"
variation 1928
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1194364986"
variation 1929
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2543271122"
variation 1930
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:2543271114"
variation 1934
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:774002945"
variation 1937
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1260717996"
variation 1938
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1212784968"
variation 1940
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:2543271093"
variation 1941
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2543271090"
variation 1943
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:768078789"
variation 1944
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950735401"
variation 1949
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2543271079"
variation 1950
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:192495200"
variation 1951
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:779420556"
variation 1952
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2543271060"
variation 1954
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1950735266"
variation 1957..1961
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="gc"
/replace="gccgc"
/db_xref="dbSNP:1218603125"
variation 1959
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:769922499"
variation 1960
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:745735958"
variation 1962
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2543271039"
variation 1963
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1339131647"
variation 1966
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:1188833829"
variation 1967
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950735030"
variation 1968
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1295444518"
variation 1970..1974
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="gaaag"
/replace="gaaagaaag"
/db_xref="dbSNP:2543271017"
variation 1970
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1449229353"
variation 1975
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1950734903"
variation 1976
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1340024053"
variation 1979
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950734826"
variation 1982
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:146332668"
variation 1983
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:371841032"
variation 1985
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1401175113"
variation 1986
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:752894210"
variation 1987
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:779235326"
exon 1988..11228
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/inference="alignment:Splign:2.1.0"
variation 1988
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2543265833"
variation 1991
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2543265831"
variation 1994
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1456116703"
variation 1995..1996
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="aa"
/replace="aaa"
/db_xref="dbSNP:2543265813"
variation 1996
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:549826875"
variation 1998
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1950704889"
variation 1999
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1223009144"
variation 2000
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:772496941"
variation 2001
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2543265793"
variation 2003
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1950704757"
variation 2007
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1950704725"
variation 2008
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950704692"
variation 2010
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:2543265773"
variation 2012
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2543265769"
variation 2013
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1288110354"
variation 2014
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1190631767"
variation 2016
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2543265756"
variation 2018
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:200441646"
variation 2019
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:2543265747"
variation 2026
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2136907624"
variation 2027
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:2543265744"
variation 2028
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:2543265741"
variation 2030
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:1950704521"
variation 2031
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1242787279"
variation 2032
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950704441"
variation 2033
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2543265729"
variation 2035
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2543265725"
variation 2036
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2543265720"
variation 2037
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="aa"
/db_xref="dbSNP:2543265715"
variation 2037
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2543265708"
variation 2038
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:776670620"
variation 2039
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:770961851"
variation 2042..2044
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="cc"
/replace="ccc"
/db_xref="dbSNP:2543265676"
variation 2042
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1238046110"
variation 2043
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2543265683"
variation 2045
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:746869999"
variation 2046
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:777416500"
variation 2047
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:755292850"
variation 2048
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:973123804"
variation 2050
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:375664747"
variation 2052
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2543265648"
variation 2053..2055
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="tt"
/replace="ttt"
/db_xref="dbSNP:1566171684"
variation 2053
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:2543265645"
variation 2056
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:780118329"
variation 2057
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2543265634"
variation 2060
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1293032557"
variation 2061
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:756135373"
variation 2062..2063
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="tg"
/db_xref="dbSNP:1950704004"
variation 2062
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2543265622"
variation 2063
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2543265619"
variation 2067
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:750955936"
variation 2068
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1157735470"
variation 2069
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:531300162"
variation 2072
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:757695645"
variation 2073
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:113800546"
variation 2074
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:2543265597"
variation 2076
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:752032125"
variation 2077
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:549782692"
variation 2078..2081
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="gt"
/replace="gtgt"
/db_xref="dbSNP:2543265574"
variation 2078
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:762683133"
variation 2081
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2543265571"
variation 2085
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2543265566"
variation 2091..2093
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="aca"
/db_xref="dbSNP:2543265555"
variation 2092
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:2543265561"
variation 2093
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2543265548"
variation 2094
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2543265545"
variation 2095
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1314603974"
variation 2096
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950703637"
variation 2099..2100
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="aa"
/replace="aaa"
/db_xref="dbSNP:1950703539"
variation 2099
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1353651008"
variation 2100
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1286369531"
variation 2101
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1045979"
variation 2102
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:2543265480"
variation 2104
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:954494653"
variation 2105
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:749186808"
variation 2107
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1283042988"
variation 2109
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2543265457"
variation 2110
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1237120100"
variation 2111
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1348995249"
variation 2112
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2136907397"
variation 2113
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1593437486"
variation 2115
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2543265433"
variation 2116
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1030178377"
variation 2120
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2543265418"
variation 2121
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="a"
/db_xref="dbSNP:1950703000"
variation 2121
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2543265409"
variation 2122
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="g"
/db_xref="dbSNP:1950702946"
variation 2122
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:2543265398"
variation 2123..2127
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="ccccc"
/replace="ccccccc"
/db_xref="dbSNP:1950702782"
variation 2123
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:2543265392"
variation 2124
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950702902"
variation 2125
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1950702832"
variation 2127
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2543265377"
variation 2128
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:925838751"
variation 2129
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:2543265363"
variation 2131
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1361292300"
variation 2132
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:2543265345"
variation 2133
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1593437462"
variation 2135
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:2543265335"
variation 2137
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:974644686"
variation 2138
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2543265327"
variation 2139..2143
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="acgca"
/db_xref="dbSNP:1950702436"
variation 2139
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2543265322"
variation 2140..2142
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="cgc"
/replace="cgcgc"
/db_xref="dbSNP:2543265289"
variation 2140
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:567430632"
variation 2141
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1341331550"
variation 2142
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:2543265277"
variation 2145
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:911586191"
variation 2148
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:542153503"
variation 2149
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:2543265251"
variation 2151
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1156419163"
variation 2152
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1435059615"
variation 2153
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1593437426"
variation 2155
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:370209943"
variation 2157
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:950536054"
variation 2158
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950702021"
variation 2159
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2543265211"
variation 2162
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:559705268"
variation 2164
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1010901456"
variation 2166
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2543265196"
variation 2167
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950701848"
variation 2168
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1298882440"
variation 2170
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:893810615"
variation 2174
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2543265177"
variation 2176
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:963549804"
variation 2178
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:2543265171"
variation 2180
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:2543265168"
variation 2182
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2543265159"
variation 2183
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:2543265152"
variation 2184..2185
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="ct"
/replace="ctct"
/db_xref="dbSNP:2136907189"
variation 2184
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="c"
/db_xref="dbSNP:2543265147"
variation 2184
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:2543265140"
variation 2185..2187
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="t"
/replace="ttt"
/replace="ttttt"
/db_xref="dbSNP:3832804"
variation 2185
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2543265128"
variation 2185
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="t"
/replace="tgt"
/db_xref="dbSNP:2136907182"
variation 2186
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="t"
/replace="tat"
/db_xref="dbSNP:2136907172"
variation 2188
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1593437365"
variation 2189
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:111820152"
variation 2190
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1052601435"
variation 2191
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1950701329"
variation 2192
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1414983132"
variation 2193
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950701238"
variation 2194
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="t"
/replace="tt"
/db_xref="dbSNP:1950701181"
variation 2195
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:2543265067"
variation 2197
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2543265057"
variation 2198
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:935595520"
variation 2199..2202
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="gaga"
/replace="gagaga"
/db_xref="dbSNP:1950701113"
variation 2202
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:2543265041"
variation 2203..2205
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="cc"
/replace="ccc"
/db_xref="dbSNP:1418783722"
variation 2205
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:2543265024"
variation 2207
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:2543265019"
variation 2208
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950701021"
variation 2209
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1002477975"
variation 2211
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2543265006"
variation 2212
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:2543265002"
variation 2216
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1278595598"
variation 2218
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1347878070"
variation 2219..2223
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="gggg"
/replace="ggggg"
/db_xref="dbSNP:1950700679"
variation 2219
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:541179525"
variation 2220
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1950700733"
variation 2223
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:576945941"
variation 2225
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:769326943"
variation 2226
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:892514179"
variation 2227
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1054288089"
variation 2231
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:2543264947"
variation 2232
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:367620504"
variation 2233
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:916367947"
variation 2234..2239
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="ccctcc"
/db_xref="dbSNP:2543264923"
variation 2236
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:973064787"
variation 2237
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:2543264926"
variation 2240
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:2543264920"
variation 2242
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1038910312"
variation 2243
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:963001005"
variation 2244..2245
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="cc"
/replace="ga"
/db_xref="dbSNP:796574941"
variation 2244
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950700117"
variation 2245
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:943323229"
variation 2246
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2543264904"
variation 2247
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950699977"
variation 2248
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950699935"
variation 2250
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2543264891"
variation 2252
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950699905"
variation 2254
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2543264881"
variation 2255
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1950699872"
variation 2258
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:370314942"
variation 2259
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="cc"
/db_xref="dbSNP:2543264865"
variation 2259
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950699794"
variation 2260
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950699755"
variation 2261
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:182916402"
variation 2262
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:3741490"
variation 2266..2286
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="tggcatcagcagcagagacga"
/db_xref="dbSNP:2543264795"
variation 2267
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1443374356"
variation 2268
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:2543264830"
variation 2269
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950699663"
variation 2271
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2136906865"
variation 2273
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:983339952"
variation 2276
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1950699592"
variation 2278
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1301770978"
variation 2284
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:987116079"
variation 2285
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950699497"
variation 2287
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:554895850"
variation 2289
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2136906816"
variation 2290
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950699427"
variation 2294
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1950699392"
variation 2299
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1298316988"
variation 2302
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950699320"
variation 2304
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:75237791"
variation 2305
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:746850522"
variation 2307
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1353265460"
variation 2308
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:777597930"
variation 2309
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:973165920"
variation 2313
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:758214417"
variation 2314
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:996057076"
variation 2316
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:192844482"
variation 2317..2321
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="gag"
/replace="gagag"
/db_xref="dbSNP:1423726431"
variation 2317
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:547619077"
variation 2323
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:2136906701"
variation 2324
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:2543264711"
variation 2325
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1010952147"
variation 2326
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1002451487"
variation 2329
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950698849"
variation 2331
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2543264691"
variation 2332
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:893777773"
variation 2336
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1030977492"
variation 2338
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1163686844"
variation 2339
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:2543264681"
variation 2343
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:2543264679"
variation 2345..2348
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="ttt"
/replace="tttt"
/db_xref="dbSNP:2543264673"
variation 2348
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950698740"
variation 2349
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1950698712"
variation 2350
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:781543889"
variation 2351
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:906815915"
variation 2352
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:2136906626"
variation 2355
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1415593537"
variation 2357
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1046993159"
variation 2367
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1334852400"
variation 2368
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:3741489"
variation 2371
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:2543264628"
variation 2374
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950698472"
variation 2377
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950698451"
variation 2378
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1270832087"
variation 2379
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1450666893"
variation 2381
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:4758909"
variation 2389
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1201112509"
variation 2390
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:2543264580"
variation 2391
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:2543264576"
variation 2392
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1192780707"
variation 2395
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2543264567"
variation 2399
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1950698208"
variation 2403
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1258321216"
variation 2405
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:2543264554"
variation 2407
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:112870346"
variation 2409
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1593437106"
variation 2412
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1476204979"
variation 2413
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1163079471"
variation 2415
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1593437086"
variation 2418
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:754605513"
variation 2419
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:549889950"
variation 2422
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1458219528"
variation 2429
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1413405596"
variation 2430..2434
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="ag"
/replace="aggag"
/db_xref="dbSNP:1950697843"
variation 2437
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1037421988"
variation 2439..2441
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="gag"
/db_xref="dbSNP:1272645289"
variation 2439
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950697778"
variation 2443
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1053774837"
variation 2448
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1401470577"
variation 2452
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950697578"
variation 2453
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1231595234"
variation 2456
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1161815482"
variation 2461
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1950697422"
variation 2462
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1343788492"
variation 2463
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1593437040"
variation 2464
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:941773272"
variation 2465
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:907515157"
variation 2466
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:142376269"
variation 2469
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950697143"
variation 2471..2472
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="aa"
/replace="aaa"
/db_xref="dbSNP:36039891"
variation 2471
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950697092"
variation 2475
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950696998"
variation 2479
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1950696954"
variation 2482
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:933225060"
variation 2492
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1355291257"
variation 2494
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1223981564"
variation 2504
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:923251377"
variation 2505
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:1950696730"
variation 2506
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1950696680"
variation 2508
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:755120503"
variation 2509
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:2136906288"
variation 2511
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950696585"
variation 2512
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1566171220"
variation 2516
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:964542689"
variation 2520
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:1021425081"
variation 2526..2528
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="tt"
/replace="ttt"
/db_xref="dbSNP:1950696422"
variation 2526
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950696455"
variation 2533..2540
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="ctt"
/replace="cttatctt"
/db_xref="dbSNP:943198387"
variation 2533
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1950696399"
variation 2538
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:989498094"
variation 2543
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1215845332"
variation 2546..2549
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="aaga"
/db_xref="dbSNP:2543264296"
variation 2553
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950696268"
variation 2555
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1258077252"
variation 2556
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950696224"
variation 2557
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950696187"
variation 2559
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950696162"
variation 2561
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1296311836"
variation 2563
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2136906187"
variation 2566..2568
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="t"
/replace="tgt"
/db_xref="dbSNP:2543264255"
variation 2567
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:958138392"
variation 2570
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950696070"
variation 2575..2581
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="aata"
/replace="aataata"
/db_xref="dbSNP:1950695982"
variation 2576..2585
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="ataat"
/replace="ataatataat"
/db_xref="dbSNP:1950695893"
variation 2578
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:1950696039"
variation 2580..2595
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="tataattta"
/replace="tataatttataattta"
/db_xref="dbSNP:1401013436"
variation 2580
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1486597998"
variation 2583
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950695953"
variation 2584
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:1593436977"
variation 2588
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950695859"
variation 2591
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1950695816"
variation 2592
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1030946220"
variation 2596
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950695735"
variation 2600
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1236969685"
variation 2603
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1950695685"
variation 2605
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:911779056"
variation 2606..2607
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="t"
/db_xref="dbSNP:1950695597"
variation 2606
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:1950695623"
variation 2607
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:1950695572"
variation 2608
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1179105860"
variation 2610
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1950695511"
variation 2612
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1406240647"
variation 2614
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:560709767"
variation 2615
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1950695431"
variation 2619
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:999568389"
variation 2621
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950695356"
variation 2623
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:548922117"
variation 2624
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1377843900"
variation 2625..2628
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="t"
/replace="tatt"
/db_xref="dbSNP:1950695202"
variation 2626
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:1950695263"
variation 2627
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950695232"
variation 2628..2631
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="ttga"
/db_xref="dbSNP:1950695140"
variation 2630
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1025188661"
variation 2631..2633
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="aa"
/replace="aaa"
/db_xref="dbSNP:1950695100"
variation 2639
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1331697816"
variation 2640
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:973134921"
variation 2641
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1012923039"
variation 2642
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:2136905955"
variation 2643
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950694997"
variation 2644
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:895287582"
variation 2646
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950694939"
variation 2647
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1950694917"
variation 2648
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2136905920"
variation 2649..2650
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="g"
/db_xref="dbSNP:34409499"
variation 2650
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1165063779"
variation 2655..2657
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="t"
/replace="tat"
/db_xref="dbSNP:1950694812"
variation 2656
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:2136905904"
variation 2657
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950694782"
variation 2659..2665
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="aaaaaaa"
/replace="aaaaaaaa"
/db_xref="dbSNP:1350044921"
variation 2659
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1374414628"
variation 2660
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:926776920"
variation 2665
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1280739400"
variation 2666
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1593436904"
variation 2669
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1593436894"
variation 2670
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:530330334"
variation 2671
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:971314022"
variation 2677
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1438398757"
variation 2678
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950694458"
variation 2692
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1950694435"
variation 2694
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1206923715"
variation 2695
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1231446323"
variation 2696
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1406251214"
variation 2698
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:941743070"
variation 2699
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950694296"
variation 2701
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:115799873"
variation 2702
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:541241838"
variation 2705
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950694155"
variation 2706
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:2136905761"
variation 2707
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950694126"
variation 2708
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950694099"
variation 2717
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1047424647"
variation 2719
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:932962176"
variation 2720
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:753996875"
variation 2721
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1211863620"
variation 2723
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950693980"
variation 2724
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1397721159"
variation 2725
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1489535422"
variation 2727
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1266210457"
variation 2730..2734
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="aaccg"
/db_xref="dbSNP:1950693729"
variation 2732..2733
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="atgctgctcccttgtgtgagtgaccacggccccgagcctggggctgga
cgcaggtcccagga"
/replace="gcaggtcccagga"
/replace="gtgctgctccctt"
/db_xref="dbSNP:1950693826"
variation 2732
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1316055975"
variation 2733..2734
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="acggccccgagcctggggctggacgcaggtcccaggacgtgct"
/db_xref="dbSNP:1441439409"
variation 2733
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:766575351"
variation 2734..2735
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="agcctggggctggacgcaggtcccaggacgtgctgctcccttct"
/replace="caggtcccaggacgtgctgctcccttct"
/replace="ctcccttct"
/replace="tgcattcccttct"
/replace="tgctgctcccttct"
/db_xref="dbSNP:rs1336309071"
variation 2734
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:2543263956"
variation 2735
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950693572"
variation 2735
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="gacatgctgctcccttgtgtgagtgaccacggccccgagcctggggct
ggacgcaggtcccaggacgtgctgctcccttctg"
/replace="gacgtgctgctcccttctg"
/replace="gccccgagcctggggctggacgcaggtcccaggacgtgctgctccctt
ctg"
/replace="ggctggacgcaggtcccaggacgtgctgctcccttctg"
/replace="gggctggacgcaggtcccaggacgtgctgctcccttctg"
/db_xref="dbSNP:rs1566171025"
variation 2736
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:974656529"
variation 2737
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1304579464"
variation 2740
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1593436768"
variation 2742
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1593436758"
variation 2744
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:577007021"
variation 2745
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:60054929"
variation 2746..2782
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="cggccccgagcctggggctggacgcaggtcccaggac"
/replace="cggccccgagcctggggctggacgcaggtcccaggacgtgctgctccc
ttctgtgagtgaccacggccccgagcctggggctggacgcaggtcccaggac"
/db_xref="dbSNP:1566170955"
variation 2746
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:137860747"
variation 2747
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:543507917"
variation 2748
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1339972650"
variation 2750
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1950693259"
variation 2752
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:576425597"
variation 2753
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:978587251"
variation 2756..2757
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="cc"
/db_xref="dbSNP:1950693096"
variation 2756
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:970720837"
variation 2757
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950693066"
variation 2765
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1000902244"
variation 2768
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1025409954"
variation 2769
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1012477120"
variation 2770
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="cc"
/db_xref="dbSNP:1722609409"
variation 2775
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950692922"
variation 2776
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1452627569"
variation 2777
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1950692858"
variation 2779
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:899887350"
variation 2782
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950692769"
variation 2783
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:373137192"
variation 2784..2870
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="tgctgctcccttgtgtgagtgacc"
/replace="tgctgctcccttgtgtgagtgaccgcggccccgagcctggggctggac
gcaggtcccaggacgtgctgctcccttgtgtgagtgacc"
/db_xref="dbSNP:1950691334"
variation 2786
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:554677515"
variation 2789
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:377537751"
variation 2793
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1420814830"
variation 2795..2796
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="ac"
/db_xref="dbSNP:1950692612"
variation 2796
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:796139459"
variation 2797
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1006432643"
variation 2803
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1950692520"
variation 2806
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1396446600"
variation 2807..2808
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="acggccccgagcctggggctggacgcaggtcccaggacgtgctgctcc
cttctgtgagt"
/replace="acggccccgagcctggggctggacgcaggtcccaggacgtgctgctcc
cttgtgtgagt"
/db_xref="dbSNP:1566170899"
variation 2807
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1384812230"
variation 2808..2809
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="acca"
/db_xref="dbSNP:1566170888"
variation 2808
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:15638"
variation 2809..2858
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="cggccccgagcctggggctggacgcaggtcccaggacgtgctgctccc
tt"
/replace="cggccccgagcctggggctggacgcaggtcccaggacgtgctgctccc
ttctgtgagtgaccacggccccgagcctggggctggacgcaggtcccaggacatgctg
ctcccttgtgtgagtgaccacggccccgagcctggggctggacgcaggtcccaggacg
tgctgctccctt"
/db_xref="dbSNP:2543263653"
variation 2809
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:111799372"
variation 2810
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:572274927"
variation 2811..2858
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="gccccgagcctggggctggacgcaggtcccaggacgtgctgctccctt
"
/replace="gccccgagcctggggctggacgcaggtcccaggacgtgctgctccctt
ctgtgagtgaccacggccccgagcctggggctggacgcaggtcccaggacatgctgct
cccttgtgtgagtgaccacagccccgagcctggggctggacgcaggtcccaggacgtg
ctgctccctt"
/db_xref="dbSNP:2543263649"
variation 2812
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950692211"
variation 2813
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:997687935"
variation 2815
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:376925671"
variation 2816
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1039131607"
variation 2820
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950692083"
variation 2821..2871
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="tggggctggacgcaggtcccaggacgtgctgctcccttgtgtgagtga
cca"
/db_xref="dbSNP:1566170810"
variation 2821
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:373528706"
variation 2822
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1593436635"
variation 2823..2893
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="gggctgga"
/replace="gggctggacgcaggtcccaggacgtgctgctcccttgtgtgagtgacc
acggccccaagcccagggctgga"
/db_xref="dbSNP:2543263520"
variation 2826
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1354479573"
variation 2827
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="t"
/replace="tt"
/db_xref="dbSNP:1192334475"
variation 2831
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:369891917"
variation 2832
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1950691911"
variation 2833
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1950691881"
variation 2835
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1950691853"
variation 2836
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:867795922"
variation 2843
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:187667016"
variation 2845
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1186063298"
variation 2846
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:111786421"
variation 2847..2858
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="tgctgctccctt"
/replace="tgctgctcccttctgtgagtgaccacggccccgagcctggggctggac
gcaggtcccaggacatgctgctccctt"
/db_xref="dbSNP:1950691518"
variation 2847
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950691632"
variation 2849..2850
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="a"
/db_xref="dbSNP:1950691609"
variation 2851..2852
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="gc"
/db_xref="dbSNP:1950691577"
variation 2854
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1485012640"
variation 2858
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1054216011"
variation 2859
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:75167846"
variation 2862
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950691423"
variation 2863
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950691387"
variation 2866
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950691364"
variation 2871
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1456063340"
variation 2872
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:538873969"
variation 2873
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:117246365"
variation 2874..2886
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="gccccaagcccag"
/db_xref="dbSNP:1230976787"
variation 2874
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1566170789"
variation 2875
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950691154"
variation 2876
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950691128"
variation 2877
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1007364269"
variation 2878
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1218487646"
variation 2879
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:111338463"
variation 2880
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950690986"
variation 2884
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:978174785"
variation 2885
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:8021"
variation 2887
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:917908364"
variation 2892
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950690803"
variation 2894
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1332266605"
variation 2895
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:890301777"
variation 2896
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1301350623"
variation 2900
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1593436516"
variation 2902
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950690645"
variation 2905
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1950690593"
variation 2906
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1051667411"
variation 2907
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950690530"
variation 2908
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:991258229"
variation 2909
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:959608059"
variation 2910
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1016485269"
variation 2911
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1006486333"
variation 2913
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:73489148"
variation 2914
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950690229"
variation 2917
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1950690169"
variation 2918
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1364197764"
variation 2919
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1455110594"
variation 2927
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1026915435"
variation 2929
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1359866417"
variation 2930
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1566170710"
variation 2931
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1172254217"
variation 2932
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1468017193"
variation 2933
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1950689734"
variation 2934
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1376990440"
variation 2939
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950689662"
variation 2940
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:997254637"
variation 2943
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1395673079"
variation 2944
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1378783852"
variation 2949
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="cggtc"
/db_xref="dbSNP:1950689542"
variation 2952
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950689502"
variation 2953
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:941680964"
variation 2954
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="a"
/db_xref="dbSNP:2136904893"
variation 2956
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:535014873"
variation 2958
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:2543263272"
variation 2959
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1950689402"
variation 2964
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1950689380"
variation 2965
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950689346"
variation 2972..2984
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="tg"
/replace="tggcttccgcctg"
/db_xref="dbSNP:1950689207"
variation 2972
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:1238486499"
variation 2979
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1038687461"
variation 2980
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1007221366"
variation 2981
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:182104463"
variation 2984
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:980532486"
variation 2985
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1349314061"
variation 2987
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950689114"
variation 2989
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1213577280"
variation 2995
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1436173408"
variation 2997
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950689033"
variation 2998
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:764304023"
variation 3003
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2136904817"
variation 3006
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:566065778"
variation 3008
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:2543263167"
variation 3010
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1481966746"
variation 3013
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1950688911"
variation 3016
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2136904799"
variation 3017
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950688886"
variation 3021
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1950688853"
variation 3024
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1199546557"
variation 3027
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1950688798"
variation 3028
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:892808322"
variation 3029..3033
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="ttttt"
/replace="tttttt"
/db_xref="dbSNP:1950688694"
variation 3032
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:949556782"
variation 3034..3035
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="gg"
/db_xref="dbSNP:1176616028"
variation 3036..3043
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="aaaa"
/replace="aaaaaa"
/replace="aaaaaaa"
/replace="aaaaaaaa"
/replace="aaaaaaaaa"
/db_xref="dbSNP:rs957212862"
variation 3036
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1265543823"
variation 3037
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1054268966"
variation 3038
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:934594162"
variation 3039
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1488453973"
variation 3044
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:191072646"
variation 3045..3050
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="ttttt"
/replace="tttttt"
/replace="ttttttt"
/db_xref="dbSNP:1566170618"
variation 3047
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1256563011"
variation 3049..3055
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="tt"
/replace="ttatctt"
/db_xref="dbSNP:1950688278"
variation 3051
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:566122046"
variation 3054
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:949484292"
variation 3055
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1950688259"
variation 3056
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950688232"
variation 3068
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950688210"
variation 3069
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1018288530"
variation 3070
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1950688147"
variation 3071
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950688117"
variation 3076
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1299758456"
variation 3077
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:549120489"
variation 3085
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950688014"
variation 3087
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:2543263003"
variation 3090
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:918030300"
variation 3092
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:565128269"
variation 3096
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1458856890"
variation 3104..3111
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="cttct"
/replace="cttcttct"
/db_xref="dbSNP:1468716986"
variation 3105
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:937960418"
variation 3106
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:909224402"
variation 3107
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1226033314"
variation 3110
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1046106"
variation 3112
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950687714"
variation 3117
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1315555821"
variation 3118
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950687665"
variation 3119
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1279655347"
variation 3120
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1950687603"
variation 3121
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:985017981"
variation 3122
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1950687569"
variation 3129
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:1950687539"
variation 3130
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1432491382"
variation 3133
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:753726528"
variation 3135
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1950687442"
variation 3143
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1425798710"
variation 3145
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2136904528"
variation 3149
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950687386"
variation 3151
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:529547282"
variation 3154..3171
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="ctg"
/replace="ctgagaagcagcaatctg"
/db_xref="dbSNP:1950687169"
variation 3154
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:148270257"
variation 3156
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:11542904"
variation 3157
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2543262835"
variation 3166
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2543262832"
variation 3167
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:2136904496"
variation 3169
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:976689419"
variation 3170
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950687203"
variation 3171
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:2136904480"
variation 3172
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950687133"
variation 3173
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1950687101"
variation 3175
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:2543262791"
variation 3177
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:965819930"
variation 3179
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1950687045"
variation 3180
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2543262776"
variation 3187
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="g"
/db_xref="dbSNP:897708347"
variation 3187
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1367604138"
variation 3190
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1037632913"
variation 3192
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950686909"
variation 3194
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950686881"
variation 3195
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950686849"
variation 3201
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2543262737"
variation 3203
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2543262728"
variation 3205
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:941651179"
variation 3206
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1046130"
regulatory 3208..3213
/regulatory_class="polyA_signal_sequence"
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/note="hexamer: AATAAA"
variation 3208
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1950686736"
variation 3209
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950686709"
variation 3214
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:904877930"
variation 3215
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1017734390"
variation 3219
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:376262240"
variation 3220
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1007273719"
variation 3221
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:892777244"
variation 3222
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:561407931"
variation 3226
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1244757352"
variation 3227
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2543262675"
variation 3228
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1298125618"
variation 3229
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:998710936"
variation 3231
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950686377"
polyA_site 3233
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/note="major polyA site"
variation 3233
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:903128041"
variation 3234
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1425875346"
variation 3236
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1950686306"
variation 3237
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1950686271"
variation 3239
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1045562980"
variation 3240
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1418900738"
variation 3242
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1052992664"
variation 3243
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1474998170"
variation 3246
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1349601661"
variation 3248
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1950686130"
variation 3250
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:542673371"
variation 3251
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:55996389"
variation 3252
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1355766739"
variation 3253
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1235119201"
variation 3255
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1055589435"
variation 3256
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="t"
/db_xref="dbSNP:2136904288"
variation 3256
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="t"
/replace="tt"
/db_xref="dbSNP:3832803"
variation 3257
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:202138339"
variation 3259
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950685865"
variation 3261..3262
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="ct"
/db_xref="dbSNP:1216443038"
variation 3263
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1288137232"
variation 3265
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1950685799"
variation 3266
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950685779"
variation 3268
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1593435993"
variation 3269
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1487250355"
variation 3272..3275
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="cccc"
/replace="ccccc"
/db_xref="dbSNP:979672401"
variation 3274
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:865810935"
variation 3275
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:2136904228"
variation 3277
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1256714665"
variation 3279
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:963993261"
variation 3280
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:911248729"
variation 3282
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:909191674"
variation 3283
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1259444324"
variation 3284
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1950685535"
variation 3286
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2543262419"
variation 3289
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1218782120"
variation 3290..3291
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="gg"
/db_xref="dbSNP:1359225076"
variation 3291
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:554139960"
variation 3293
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1419620172"
variation 3295
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1297103590"
variation 3296
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2136904163"
variation 3303
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2543262386"
variation 3304
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2543262382"
variation 3308
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2543262377"
variation 3309
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1950685428"
variation 3311
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:545310763"
variation 3312
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1282117653"
variation 3321
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:745444738"
variation 3329
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950685332"
variation 3340
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1950685303"
variation 3341
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="t"
/replace="tt"
/db_xref="dbSNP:1282020007"
variation 3351
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:1950685254"
variation 3352
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950685233"
variation 3354
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1950685209"
variation 3355
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950685189"
variation 3360
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1950685164"
variation 3361
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950685145"
variation 3365
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:577967891"
variation 3375
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2136904095"
variation 3381
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1240653048"
variation 3385..3442
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="t"
/replace="tctcttcattctgccaatgctgggaagccacaacctgttcatccagtg
tggaggcttt"
/db_xref="dbSNP:1950684561"
variation 3386
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1311180255"
variation 3390
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:2543262310"
variation 3391
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950685066"
variation 3393
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1247374518"
variation 3396
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1950685020"
variation 3398..3401
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="ccaa"
/db_xref="dbSNP:1950684955"
variation 3398
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950685000"
variation 3400
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1485422316"
variation 3401
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:556395444"
variation 3402
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:1950684899"
variation 3404
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1281132291"
variation 3406
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1566170285"
variation 3412
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:966577614"
variation 3414
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1017787041"
variation 3416..3417
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="aa"
/replace="aaa"
/db_xref="dbSNP:1208309050"
variation 3424
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950684763"
variation 3425
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:776204190"
variation 3430
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950684723"
variation 3431
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950684699"
variation 3432
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1445228645"
variation 3434
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:866682414"
variation 3437
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:985821899"
variation 3439
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1332126659"
variation 3440
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1593435782"
variation 3445
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950684532"
variation 3447
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:2543262223"
variation 3451
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1461026396"
variation 3452
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:117630891"
variation 3453
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:961887868"
variation 3456
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:749026459"
variation 3457
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1016168618"
variation 3460
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1165245685"
variation 3461
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1950684334"
variation 3462
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1174773582"
variation 3465
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1950684286"
variation 3466
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1425293288"
variation 3469
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1950684242"
variation 3473
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1415734691"
variation 3474
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1006166894"
variation 3475
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1473634704"
variation 3476
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1032626970"
variation 3477
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1447047391"
variation 3483
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:567264574"
variation 3484
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:555424343"
variation 3485
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950684045"
variation 3487..3680
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="agtttgtgca"
/replace="agtttgtgcaagggtggggctgagaggggaggtcccgtgttagtgcag
gggtgaggccgggaggggaggtcccgagtttgtgtaggggcgaggctgagcagggagg
ttctgagttagtgcaggggcgaggctgagcagggaggtcccgagttagtgcaggggcg
aggctaagggggaggtcccaagtttgtgca"
/db_xref="dbSNP:2543261537"
variation 3487
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1275321275"
variation 3490
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950683990"
variation 3492
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950683960"
variation 3495
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1239986132"
variation 3498
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2543262106"
variation 3502..3576
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="ggggctgagaggggaggtcccgtgttagtgcaggggtgaggccgggag
gggaggtcccgagtttgtgtaggggcg"
/db_xref="dbSNP:2543261929"
variation 3502
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950683909"
variation 3503
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1347008032"
variation 3504..3780
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="ggctgagaggggaggtccc"
/replace="ggctgagaggggaggtcccgtgttagtgcaggggtgaggccgggaggg
gaggtcccgagtttgtgtaggggcgaggctgagcagggaggttctgagttagtgcagg
ggcgaggctgagcagggaggtcccgagttagtgcaggggcgaggctaagggggaggtc
ccaagtttgtgcaggggtgaggctgagcagggaggtcccaagttagtgcaggggcgag
gctgagaggggagatcccgagtttgtgcaggggcgaggctgagaggggaggtccc"
/db_xref="dbSNP:1950678192"
variation 3504..3738
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="ggctgagaggggag"
/replace="ggctgagaggggaggtcccgtgttagtgcaggggtgaggccgggaggg
gaggtcccgagtttgtgtaggggcgaggctgagcagggaggttctgagttagtgcagg
ggcgaggctgagcagggaggtcccgagttagtgcaggggcgaggctaagggggaggtc
ccaagtttgtgcaggggtgaggctgagcagggaggtcccaagttagtgcaggggcgag
gctgagaggggag"
/db_xref="dbSNP:1950679060"
variation 3504
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1217580586"
variation 3507
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1277993800"
variation 3508..3512
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="gag"
/replace="gagag"
/db_xref="dbSNP:1198698360"
variation 3510
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1024607726"
variation 3512..3669
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="ggggaggtccc"
/replace="ggggaggtcccgtgttagtgcaggggtgaggccgggaggggaggtccc
gagtttgtgtaggggcgaggctgagcagggaggttctgagttagtgcaggggcgaggc
tgagcagggaggtcccgagttagtgcaggggcgaggctaagggggaggtccc"
/db_xref="dbSNP:2543261579"
variation 3512
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1438663278"
variation 3513..3634
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="gggaggtcccg"
/replace="gggaggtcccgtgttagtgcaggggtgaggccgggaggggaggtcccg
agtttgtgtaggggcgaggctgagcagggaggttctgagttagtgcaggggcgaggct
gagcagggaggtcccg"
/db_xref="dbSNP:2543261747"
variation 3517..3520
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="ggtc"
/replace="ggtcggtc"
/db_xref="dbSNP:1950683709"
variation 3519
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1834228183"
variation 3522
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1467655689"
variation 3523..3597
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="gtgttagtgcaggggtgaggccgggaggggaggtcccgagtttgtgta
ggggcgaggctgagcagggaggttctg"
/db_xref="dbSNP:2543261887"
variation 3523
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:533581400"
variation 3524..3707
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="tgttagtgcaggggtgaggccgggaggggaggtcccgagtttgtgtag
gggcgaggctgagcagggaggttctgagttagtgcaggggcgaggctgagcagggagg
tcccgagttagtgcaggggcgaggctaagggggaggtcccaagtttgtgcaggggtga
ggctgagcagggaggtccca"
/db_xref="dbSNP:2543261408"
variation 3524
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:1211266849"
variation 3525..3803
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="gttagtgcaggggtgaggccg"
/replace="gttagtgcaggggtgaggccgggaggggaggtcccgagtttgtgtagg
ggcgaggctgagcagggaggttctgagttagtgcaggggcgaggctgagcagggaggt
cccgagttagtgcaggggcgaggctaagggggaggtcccaagtttgtgcaggggtgag
gctgagcagggaggtcccaagttagtgcaggggcgaggctgagaggggagatcccgag
tttgtgcaggggcgaggctgagaggggaggtccctagttagtgcaggggtgaggccg"
/db_xref="dbSNP:2543261065"
variation 3525..3721
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="gttagtgcagggg"
/replace="gttagtgcaggggtgaggccgggaggggaggtcccgagtttgtgtagg
ggcgaggctgagcagggaggttctgagttagtgcaggggcgaggctgagcagggaggt
cccgagttagtgcaggggcgaggctaagggggaggtcccaagtttgtgcaggggtgag
gctgagcagggaggtcccaagttagtgcagggg"
/db_xref="dbSNP:2543261356"
variation 3525
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1477323731"
variation 3528
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:1950683507"
variation 3529..3690
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="gtgcaggggtgaggc"
/replace="gtgcaggggtgaggccgggaggggaggtcccgagtttgtgtaggggcg
aggctgagcagggaggttctgagttagtgcaggggcgaggctgagcagggaggtcccg
agttagtgcaggggcgaggctaagggggaggtcccaagtttgtgcaggggtgaggc"
/db_xref="dbSNP:2543261483"
variation 3529
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1950683465"
variation 3532
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950683433"
variation 3534..3552
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="ggg"
/replace="ggggtgaggccgggagggg"
/db_xref="dbSNP:2543261969"
variation 3535
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950683395"
variation 3536
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950683352"
variation 3538
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:57466534"
variation 3539..3654
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="gaggc"
/replace="gaggccgggaggggaggtcccgagtttgtgtaggggcgaggctgagca
gggaggttctgagttagtgcaggggcgaggctgagcagggaggtcccgagttagtgca
ggggcgaggc"
/db_xref="dbSNP:2543261653"
variation 3543
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950683265"
variation 3544
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1357421669"
variation 3545..3547
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="ggg"
/db_xref="dbSNP:1950683096"
variation 3545
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:566128545"
variation 3546
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1465823754"
variation 3547..3738
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="gaggggag"
/replace="gaggggaggtcccgagtttgtgtaggggcgaggctgagcagggaggtt
ctgagttagtgcaggggcgaggctgagcagggaggtcccgagttagtgcaggggcgag
gctaagggggaggtcccaagtttgtgcaggggtgaggctgagcagggaggtcccaagt
tagtgcaggggcgaggctgagaggggag"
/db_xref="dbSNP:2543261294"
variation 3547
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2543261989"
variation 3549..3669
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="ggggaggtccc"
/replace="ggggaggtcccgagtttgtgtaggggcgaggctgagcagggaggttct
gagttagtgcaggggcgaggctgagcagggaggtcccgagttagtgcaggggcgaggc
taagggggaggtccc"
/db_xref="dbSNP:2543261575"
variation 3549..3550
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="ca"
/db_xref="dbSNP:1950683001"
variation 3549
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1172319141"
variation 3553
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1950682967"
variation 3555
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1950682929"
variation 3556..3752
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="tcccgagtttgtg"
/replace="tcccgagtttgtgtaggggcgaggctgagcagggaggttctgagttag
tgcaggggcgaggctgagcagggaggtcccgagttagtgcaggggcgaggctaagggg
gaggtcccaagtttgtgcaggggtgaggctgagcagggaggtcccaagttagtgcagg
ggcgaggctgagaggggagatcccgagtttgtg"
/db_xref="dbSNP:1950678806"
variation 3557
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1593435609"
variation 3559
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1397873854"
variation 3560
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1238517384"
variation 3561..3711
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="agtt"
/replace="agtttgtgtaggggcgaggctgagcagggaggttctgagttagtgcag
gggcgaggctgagcagggaggtcccgagttagtgcaggggcgaggctaagggggaggt
cccaagtttgtgcaggggtgaggctgagcagggaggtcccaagtt"
/db_xref="dbSNP:1950679736"
variation 3561..3678
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="agtttgtg"
/replace="agtttgtgtaggggcgaggctgagcagggaggttctgagttagtgcag
gggcgaggctgagcagggaggtcccgagttagtgcaggggcgaggctaagggggaggt
cccaagtttgtg"
/db_xref="dbSNP:2543261549"
variation 3563..3565
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="t"
/replace="tt"
/replace="ttt"
/db_xref="dbSNP:1332824647"
variation 3565
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:60360004"
variation 3566..3715
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="gtg"
/replace="gtgtaggggcgaggctgagcagggaggttctgagttagtgcaggggcg
aggctgagcagggaggtcccgagttagtgcaggggcgaggctaagggggaggtcccaa
gtttgtgcaggggtgaggctgagcagggaggtcccaagttagtg"
/db_xref="dbSNP:2543261377"
variation 3566
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1379727237"
variation 3568
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1055659515"
variation 3569
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="t"
/db_xref="dbSNP:1950682702"
variation 3569
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:60941050"
variation 3570..3768
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="aggggcgaggctgag"
/replace="aggggcgaggctgagcagggaggttctgagttagtgcaggggcgaggc
tgagcagggaggtcccgagttagtgcaggggcgaggctaagggggaggtcccaagttt
gtgcaggggtgaggctgagcagggaggtcccaagttagtgcaggggcgaggctgagag
gggagatcccgagtttgtgcaggggcgaggctgag"
/db_xref="dbSNP:1950678568"
variation 3570..3731
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="aggggcgaggctgag"
/replace="aggggcgaggctgagcagggaggttctgagttagtgcaggggcgaggc
tgagcagggaggtcccgagttagtgcaggggcgaggctaagggggaggtcccaagttt
gtgcaggggtgaggctgagcagggaggtcccaagttagtgcaggggcgaggctgag"
/db_xref="dbSNP:1950679211"
variation 3570..3655
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="aggggcgaggct"
/replace="aggggcgaggctgagcagggaggttctgagttagtgcaggggcgaggc
tgagcagggaggtcccgagttagtgcaggggcgaggct"
/db_xref="dbSNP:2543261647"
variation 3570..3630
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="aggggcgaggctgagcagggaggt"
/replace="aggggcgaggctgagcagggaggttctgagttagtgcaggggcgaggc
tgagcagggaggt"
/db_xref="dbSNP:2543261795"
variation 3572
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950682654"
variation 3575
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:186414211"
variation 3576..3703
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="gaggctgagcagggaggt"
/replace="gaggctgagcagggaggttctgagttagtgcaggggcgaggctgagca
gggaggtcccgagttagtgcaggggcgaggctaagggggaggtcccaagtttgtgcag
gggtgaggctgagcagggaggt"
/db_xref="dbSNP:1950679907"
variation 3576
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:887894348"
variation 3577
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950682562"
variation 3585
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1325703753"
variation 3586
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1593435541"
variation 3587
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2543261908"
variation 3588..3625
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="gg"
/replace="ggaggttctgagttagtgcaggggcgaggctgagcagg"
/db_xref="dbSNP:1200441061"
variation 3589
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1950682527"
variation 3592
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1950682500"
variation 3594
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:117183760"
variation 3595
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950682449"
variation 3596
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:117783146"
variation 3597..3655
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="gagttagtgcaggggcgaggct"
/replace="gagttagtgcaggggcgaggctgagcagggaggtcccgagttagtgca
ggggcgaggct"
/db_xref="dbSNP:2543261645"
variation 3597
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950682399"
variation 3598..3795
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="agttagtgcagggg"
/replace="agttagtgcaggggcgaggctgagcagggaggtcccgagttagtgcag
gggcgaggctaagggggaggtcccaagtttgtgcaggggtgaggctgagcagggaggt
cccaagttagtgcaggggcgaggctgagaggggagatcccgagtttgtgcaggggcga
ggctgagaggggaggtccctagttagtgcagggg"
/db_xref="dbSNP:1950677974"
variation 3598..3731
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="agttagtgcaggggcgaggctgag"
/replace="agttagtgcaggggcgaggctgagcagggaggtcccgagttagtgcag
gggcgaggctaagggggaggtcccaagtttgtgcaggggtgaggctgagcagggaggt
cccaagttagtgcaggggcgaggctgag"
/db_xref="dbSNP:1950679195"
variation 3601
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1049087786"
variation 3603..3768
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="gtgcaggggcgaggctgag"
/replace="gtgcaggggcgaggctgagcagggaggtcccgagttagtgcaggggcg
aggctaagggggaggtcccaagtttgtgcaggggtgaggctgagcagggaggtcccaa
gttagtgcaggggcgaggctgagaggggagatcccgagtttgtgcaggggcgaggctg
ag"
/db_xref="dbSNP:1950678534"
variation 3603..3684
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="gtgcagggg"
/replace="gtgcaggggcgaggctgagcagggaggtcccgagttagtgcaggggcg
aggctaagggggaggtcccaagtttgtgcagggg"
/db_xref="dbSNP:2543261525"
variation 3605
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:183198904"
variation 3612
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:532675767"
variation 3613..3706
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="gaggctgagcagggaggtccc"
/replace="gaggctgagcagggaggtcccgagttagtgcaggggcgaggctaaggg
ggaggtcccaagtttgtgcaggggtgaggctgagcagggaggtccc"
/db_xref="dbSNP:1950679836"
variation 3613
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="g"
/db_xref="dbSNP:1382041557"
variation 3613
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:61466030"
variation 3615
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:2543261857"
variation 3616
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:571562352"
variation 3617
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1179209743"
variation 3621
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="gaagggaggtcccgagttagtgcagggg"
/db_xref="dbSNP:2136903562"
variation 3622..3623
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="ca"
/db_xref="dbSNP:1244486668"
variation 3622
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="c"
/db_xref="dbSNP:1950682173"
variation 3622
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:60471631"
variation 3623
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1464771766"
variation 3624..3780
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="gggaggtccc"
/replace="gggaggtcccgagttagtgcaggggcgaggctaagggggaggtcccaa
gtttgtgcaggggtgaggctgagcagggaggtcccaagttagtgcaggggcgaggctg
agaggggagatcccgagtttgtgcaggggcgaggctgagaggggaggtccc"
/db_xref="dbSNP:1950678162"
variation 3624..3649
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="gggaggtcccgagttagtgcaggggc"
/replace="gggaggtcccgagttagtgcaggggcaacgctgagaaggggaggtccc
gagttagtgcaggggc"
/replace="gggaggtcccgagttagtgcaggggcaaggctgagaaggggaggtccc
gagttagtgcaggggc"
/db_xref="dbSNP:57154544"
variation 3624..3633
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="gggaggtccc"
/replace="gggaggtcccaagttagtgcaggggcaaggctgagaaggggaggtccc
"
/db_xref="dbSNP:1950681703"
variation 3624..3632
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="gggaggtcc"
/replace="gggaggtccagagttagtgcaggggcaaggctgagaaggggaggtcc"
/replace="gggaggtccggagttagtgcagggacaaggctgagaaggggaggtcc"
/replace="gggaggtccggagttagtgcaggggcaaggctgagaaggggaggtcc"
/db_xref="dbSNP:1223022795"
variation 3624..3631
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="gggaggtc"
/replace="gggaggtctggagttagtgcaggggcaaggctgagaaggggaggtc"
/db_xref="dbSNP:1950681772"
variation 3624..3630
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="gggaggt"
/replace="gggaggttctgagttagtgcaggggcaaggctgagaaggggaggt"
/db_xref="dbSNP:2543261791"
variation 3624..3627
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="ggga"
/replace="gggatgtcccgagttagtgcaggggcaaggctgagaagggga"
/db_xref="dbSNP:1950681946"
variation 3624..3626
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="ggg"
/replace="gggg"
/replace="gggtcccgagttagtgcaggggcaaggctgagaagggg"
/db_xref="dbSNP:66881773"
variation 3624..3625
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="gg"
/replace="ggaaggtcccgagttagtgcaggggcaaggctgagaaggg"
/db_xref="dbSNP:1950682049"
variation 3625..3629
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="gg"
/replace="ggagg"
/db_xref="dbSNP:1950681843"
variation 3626..3627
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="t"
/db_xref="dbSNP:1555268058"
variation 3626
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1950681984"
variation 3627..3649
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="aggtcccgagttagtgcaggggc"
/replace="aggtcccgagttagtgcaggggcaaggctgagaagggaaggtcccgag
ttagtgcaggggc"
/db_xref="dbSNP:1950681403"
variation 3627
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="aa"
/db_xref="dbSNP:1950681919"
variation 3627
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1593435441"
variation 3628..3649
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="ggtcccgagttagtgcaggggc"
/replace="ggtcccgagttagtgcaggggcaaggctgagaagggggggtcccgagt
tagtgcaggggc"
/db_xref="dbSNP:1950681382"
variation 3628..3629
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="gg"
/replace="ggg"
/db_xref="dbSNP:1950681817"
variation 3628
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1403536986"
variation 3629..3649
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="gtcccgagttagtgcaggggc"
/replace="gtcccgagttagtgcaggggcaaggctgagaaggggaagtcccgagtt
agtgcaggggc"
/db_xref="dbSNP:1950681357"
variation 3629..3632
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="gtcc"
/replace="gtccggagttagtgcaggggcaaggctgagaaggggaagtcc"
/db_xref="dbSNP:2543261765"
variation 3630..3748
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="tcccgagtt"
/replace="tcccgagttagtgcaggggcgaggctaagggggaggtcccaagtttgt
gcaggggtgaggctgagcagggaggtcccaagttagtgcaggggcgaggctgagaggg
gagatcccgagtt"
/db_xref="dbSNP:1950678909"
variation 3630
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1322760725"
variation 3631..3649
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="cccgagttagtgcaggggc"
/replace="cccgagttagtgcaggggcaaggctgagaaggggagggcccgagttag
tgcaggggc"
/db_xref="dbSNP:1950681334"
variation 3632
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1341031292"
variation 3633
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:116330402"
variation 3634..3649
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="gagttagtgcaggggc"
/replace="gagttagtgcaggggcaaggctgagaaggggaggtccagagttagtgc
aggggc"
/replace="gagttagtgcaggggcaaggctgagaaggggaggtcctgagttagtgc
aggggc"
/db_xref="dbSNP:767254938"
variation 3634
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1041001432"
variation 3635..3795
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="agttagtgcagggg"
/replace="agttagtgcaggggcgaggctaagggggaggtcccaagtttgtgcagg
ggtgaggctgagcagggaggtcccaagttagtgcaggggcgaggctgagaggggagat
cccgagtttgtgcaggggcgaggctgagaggggaggtccctagttagtgcagggg"
/db_xref="dbSNP:2543261102"
variation 3635..3728
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="agttagtgcaggggcgaggct"
/replace="agttagtgcaggggcgaggctaagggggaggtcccaagtttgtgcagg
ggtgaggctgagcagggaggtcccaagttagtgcaggggcgaggct"
/db_xref="dbSNP:1950679314"
variation 3635..3649
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="agttagtgcaggggc"
/replace="agttagtgcaggggcaaggctgagaaggggaggtcccaagttagtgca
ggggc"
/db_xref="dbSNP:1950681285"
variation 3635
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950681618"
variation 3638
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1267613131"
variation 3639..3649
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="agtgcaggggc"
/replace="agtgcaggggcaaggctgagaaggggaggtcccgagtcagtgcagggg
c"
/replace="agtgcaggggcaaggctgagaaggggaggtcccgagtgagtgcagggg
c"
/db_xref="dbSNP:1950681268"
variation 3639
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:1593435402"
variation 3640..3765
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="gtgcaggggcgaggct"
/replace="gtgcaggggcgaggctaagggggaggtcccaagtttgtgcaggggtga
ggctgagcagggaggtcccaagttagtgcaggggcgaggctgagaggggagatcccga
gtttgtgcaggggcgaggct"
/db_xref="dbSNP:2543261221"
variation 3640..3684
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="gtgcagggg"
/replace="gtgcaggggcgaggctaagggggaggtcccaagtttgtgcagggg"
/db_xref="dbSNP:2543261519"
variation 3640..3649
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="gtgcaggggc"
/replace="gtgcaggggcaaggctgagaaggggaggtcccgagtttgtgcaggggc
"
/db_xref="dbSNP:2136903384"
variation 3642
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950681563"
variation 3643
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950681543"
variation 3644..3649
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="aggggc"
/replace="aggggcaaggctgagaaggggaggtcccgagttagtgtaggggc"
/db_xref="dbSNP:1950681240"
variation 3645..3649
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="ggggc"
/replace="ggggcaaggctgagaaggggaggtcccgagttattgctggggc"
/db_xref="dbSNP:2543261689"
variation 3646
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1354640319"
variation 3647..3649
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="ggc"
/replace="ggcaaggctgagaaggggaggtcccgagttagtgcagaggc"
/db_xref="dbSNP:1950681211"
variation 3647
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950681496"
variation 3648..3753
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="gc"
/replace="gcgaggctaagggggaggtcccaagtttgtgcaggggtgaggctgagc
agggaggtcccaagttagtgcaggggcgaggctgagaggggagatcccgagtttgtgc
"
/db_xref="dbSNP:2543261253"
variation 3648..3716
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="gc"
/replace="gcgaggctaagggggaggtcccaagtttgtgcaggggtgaggctgagc
agggaggtcccaagttagtgc"
/db_xref="dbSNP:1950679583"
variation 3648..3649
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="gc"
/replace="gcaaggctgagaaggggaggtcccgagttagtgcaggagc"
/db_xref="dbSNP:1950681189"
variation 3648
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1950681472"
variation 3649..3650
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="aaggctgagaaggg"
/replace="aaggctgagaaggggaggtcccgagttagtgcaggg"
/replace="aaggctgagaaggggaggtcccgagttagtgcaggggt"
/db_xref="dbSNP:1950681131"
variation 3649
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1209790050"
variation 3650..3651
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="ca"
/db_xref="dbSNP:1950681073"
variation 3650
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:79786051"
variation 3651
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950681054"
variation 3652
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1489538599"
variation 3653..3654
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="tcccgagttagtgcaggggcgaga"
/db_xref="dbSNP:1950681008"
variation 3655..3656
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="ga"
/replace="gag"
/replace="gagaaggggaggtcccgagttagtgcaggggcgaggcg"
/db_xref="dbSNP:376942538"
variation 3656..3661
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="aagggg"
/db_xref="dbSNP:1214880110"
variation 3656
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:74997048"
variation 3658..3662
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="ggggg"
/replace="gggggg"
/db_xref="dbSNP:1370003023"
variation 3658..3659
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="a"
/replace="aa"
/db_xref="dbSNP:146529068"
variation 3658
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950680921"
variation 3659..3660
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="a"
/db_xref="dbSNP:1950680838"
variation 3659
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1950680858"
variation 3661
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1187726554"
variation 3662
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950680751"
variation 3663
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="a"
/db_xref="dbSNP:1950680726"
variation 3663
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1950680698"
variation 3664..3669
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="ggtccc"
/db_xref="dbSNP:1950680582"
variation 3664
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950680662"
variation 3665..3669
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="gtccc"
/db_xref="dbSNP:1593435321"
variation 3665
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1950680632"
variation 3666
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1471717974"
variation 3669
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1162405102"
variation 3670..3671
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="aa"
/db_xref="dbSNP:1950680473"
variation 3670
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:111391889"
variation 3673..3696
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="tttgtgcaggggtgaggctgagca"
/db_xref="dbSNP:1950680011"
variation 3675
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1018371243"
variation 3676..3801
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="gtgcaggggtgaggc"
/replace="gtgcaggggtgaggctgagcagggaggtcccaagttagtgcaggggcg
aggctgagaggggagatcccgagtttgtgcaggggcgaggctgagaggggaggtccct
agttagtgcaggggtgaggc"
/db_xref="dbSNP:2543261078"
variation 3678
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="g"
/db_xref="dbSNP:1296435999"
variation 3679
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950680393"
variation 3681
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950680364"
variation 3682
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:186710929"
variation 3683
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1396861662"
variation 3684
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950680288"
variation 3685
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1338902286"
variation 3686
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1287322125"
variation 3687
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950680191"
variation 3688
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1234210210"
variation 3691
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1310445090"
variation 3692
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1383169442"
variation 3692
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="ggg"
/db_xref="dbSNP:2543261473"
variation 3693
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:1950680091"
variation 3694
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1215009558"
variation 3695..3696
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="ca"
/db_xref="dbSNP:1950679982"
variation 3695
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1342889968"
variation 3696..3822
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="agggaggtcccaagtt"
/replace="agggaggtcccaagttagtgcaggggcgaggctgagaggggagatccc
gagtttgtgcaggggcgaggctgagaggggaggtccctagttagtgcaggggtgaggc
cgagaagggaggtcccaagtt"
/db_xref="dbSNP:2543261012"
variation 3696..3698
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="agg"
/db_xref="dbSNP:2543261434"
variation 3696
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="a"
/db_xref="dbSNP:1257887581"
variation 3696
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1200514084"
variation 3700
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:2543261430"
variation 3703..3707
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="tccca"
/db_xref="dbSNP:2543261397"
variation 3703
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1276676568"
variation 3704
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950679861"
variation 3706
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1437330525"
variation 3707
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:2076920"
variation 3708..3795
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="agttagtgcagggg"
/replace="agttagtgcaggggcgaggctgagaggggagatcccgagtttgtgcag
gggcgaggctgagaggggaggtccctagttagtgcagggg"
/db_xref="dbSNP:2543261095"
variation 3708
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:2543261396"
variation 3711
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950679702"
variation 3712
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:12825925"
variation 3713..3775
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="gtgcaggggcgaggctgagaggggag"
/replace="gtgcaggggcgaggctgagaggggagatcccgagtttgtgcaggggcg
aggctgagaggggag"
/replace="gtgcaggggcgaggctgagaggggagatcccgagtttgtgcaggggcg
aggctgagaggggagatcccgagtttgtgcaggggcgaggctgagaggggag"
/db_xref="dbSNP:1950678298"
variation 3714
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1950679634"
variation 3715
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1397864908"
variation 3716..3717
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="ca"
/db_xref="dbSNP:2543261365"
variation 3716
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1362220342"
variation 3718..3723
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="ggggcg"
/db_xref="dbSNP:1413823394"
variation 3718
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950679517"
variation 3719
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1950679493"
variation 3720..3727
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="ggcgaggc"
/replace="ggcgaggcgaggc"
/db_xref="dbSNP:1950679340"
variation 3720
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1770518966"
variation 3722
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:12815689"
variation 3723
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1466658513"
variation 3724
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950679385"
variation 3725
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950679364"
variation 3727
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:2543261332"
variation 3728
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1423053920"
variation 3729..3733
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="gag"
/replace="gagag"
/db_xref="dbSNP:1261959191"
variation 3729
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1400416338"
variation 3730
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1173793788"
variation 3731..3732
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="c"
/db_xref="dbSNP:2543261309"
variation 3732..3849
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="aggggag"
/replace="aggggagatcccgagtttgtgcaggggcgaggctgagaggggaggtcc
ctagttagtgcaggggtgaggccgagaagggaggtcccaagtttgtgcatggatgaag
ccaaaaggggag"
/db_xref="dbSNP:1950677296"
variation 3732..3769
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="aggggagatcccgagtttgtgcaggggcgaggctgaga"
/db_xref="dbSNP:1950678454"
variation 3732
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="a"
/db_xref="dbSNP:1332470640"
variation 3732
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="aa"
/db_xref="dbSNP:1566169698"
variation 3732
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:12825913"
variation 3733..3768
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="ggggagatcccgagtttgtgcaggggcgaggctgag"
/db_xref="dbSNP:1950678519"
variation 3733..3734
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="c"
/db_xref="dbSNP:2543261301"
variation 3733
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:12810751"
variation 3736
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2543261298"
variation 3739..3743
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="atccc"
/db_xref="dbSNP:2543261280"
variation 3739
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:12825910"
variation 3740
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1489438002"
variation 3741
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2543261283"
variation 3742
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950679002"
variation 3743
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1287398147"
variation 3744
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:375600964"
variation 3745..3828
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="agtttgtgca"
/replace="agtttgtgcaggggcgaggctgagaggggaggtccctagttagtgcag
gggtgaggccgagaagggaggtcccaagtttgtgca"
/db_xref="dbSNP:2543261002"
variation 3745
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:1950678934"
variation 3746..3869
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="gtttgtgcagggg"
/replace="gtttgtgcaggggcgaggctgagaggggaggtccctagttagtgcagg
ggtgaggccgagaagggaggtcccaagtttgtgcatggatgaagccaaaaggggagtt
tgcacgtttgtgcagggg"
/db_xref="dbSNP:2543260926"
variation 3749
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:12819811"
variation 3750..3795
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="gtgcagggg"
/replace="gtgcaggggcgaggctgagaggggaggtccctagttagtgcagggg"
/db_xref="dbSNP:1950677957"
variation 3750..3784
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="gt"
/replace="gtgcaggggcgaggctgagaggggaggtccctagt"
/db_xref="dbSNP:2543261127"
variation 3750
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1950678836"
variation 3753
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1441189960"
variation 3754
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:2136902940"
variation 3755..3760
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="ggggcg"
/db_xref="dbSNP:1950678673"
variation 3755
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1281409644"
variation 3756
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:944998475"
variation 3757
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1950678732"
variation 3758
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1219837449"
variation 3759
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1013335573"
variation 3760
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:112739529"
variation 3761
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:896188758"
variation 3765
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1593435121"
variation 3766..3770
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="gag"
/replace="gagag"
/db_xref="dbSNP:1375942068"
variation 3766
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2543261218"
variation 3767
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950678590"
variation 3768
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="g"
/db_xref="dbSNP:1950678498"
variation 3768
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1593435116"
variation 3769
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="a"
/db_xref="dbSNP:2543261186"
variation 3769
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="aa"
/db_xref="dbSNP:2543261184"
variation 3769
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1950678435"
variation 3770
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1276462086"
variation 3772
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1593435113"
variation 3773
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1469486487"
variation 3774
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1171600400"
variation 3775
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1052202826"
variation 3776
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:139162096"
variation 3777..3781
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="tccct"
/db_xref="dbSNP:1950678107"
variation 3778
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1368989720"
variation 3779
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:986290603"
variation 3780
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1447071019"
variation 3781..3812
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="tagttagtgcaggggtgaggccgagaagggag"
/db_xref="dbSNP:2543261041"
variation 3781
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:113103891"
variation 3782
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:1357340571"
variation 3783
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1937327190"
variation 3786
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:1222552020"
variation 3787..3876
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="gtgcaggggtgaggcc"
/replace="gtgcaggggtgaggccgagaagggaggtcccaagtttgtgcatggatg
aagccaaaaggggagtttgcacgtttgtgcaggggtgaggcc"
/db_xref="dbSNP:2543260924"
variation 3787
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2543261118"
variation 3789
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:2543261114"
variation 3790
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950678033"
variation 3791..3796
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="aggggt"
/db_xref="dbSNP:1950677940"
variation 3792..3797
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="ggggtg"
/db_xref="dbSNP:2543261085"
variation 3792
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2543261109"
variation 3794
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:925478263"
variation 3796
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1319519569"
variation 3797
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2136902781"
variation 3798
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2543261081"
variation 3801..3807
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="ccgagaa"
/db_xref="dbSNP:2543261052"
variation 3801..3802
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="cc"
/db_xref="dbSNP:1950677865"
variation 3802
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:117032655"
variation 3803
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:555579771"
variation 3804
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1422296608"
variation 3806..3807
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="aa"
/db_xref="dbSNP:1950677775"
variation 3806
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:2543261054"
variation 3807
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1168025000"
variation 3808
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1265396408"
variation 3809
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:556388372"
variation 3811
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:977147944"
variation 3812
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950677652"
variation 3814
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1194441851"
variation 3815
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:2543261030"
variation 3816
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1426132806"
variation 3818
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1478590998"
variation 3819
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1170206328"
variation 3821
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:111779210"
variation 3823
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:1950677555"
variation 3824
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1181615742"
variation 3825
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950677523"
variation 3826
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2543261004"
variation 3828..3834
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="atg"
/replace="atggatg"
/db_xref="dbSNP:1403839408"
variation 3828
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950677501"
variation 3829
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1459929360"
variation 3830
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1950677469"
variation 3832
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2543260992"
variation 3834
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:771994478"
variation 3836
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1278270568"
variation 3837
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950677371"
variation 3838
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1342048529"
variation 3840..3843
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="aaa"
/replace="aaaa"
/db_xref="dbSNP:2543260964"
variation 3841
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950677337"
variation 3842
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2136902664"
variation 3843
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2543260958"
variation 3849
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950677281"
variation 3851
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1014568743"
variation 3856
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:958676046"
variation 3857
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1272028323"
variation 3860
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1322057406"
variation 3861..3982
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="gtgcaggggtgaggcc"
/replace="gtgcaggggtgaggccaagaagggaagtcttgagttggtgcaggggtg
agggagaggggaggtcctgagtttgtgcagaggcgaggctgagaggggaggtccctaa
gtgcaggggtgaggcc"
/db_xref="dbSNP:2543260450"
variation 3865
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1950677203"
variation 3866
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1223703877"
variation 3867
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:200773842"
variation 3868
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1211443458"
variation 3877..3911
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="aagaagggaagtcttgagttggtgcaggggtgagg"
/db_xref="dbSNP:2543260870"
variation 3877
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950677139"
variation 3879
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1490165451"
variation 3880
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950677104"
variation 3881
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1437252573"
variation 3882
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950677073"
variation 3886
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1256219527"
variation 3887
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950677037"
variation 3890
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1200671899"
variation 3891..4039
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="tgagtt"
/replace="tgagttggtgcaggggtgagggagaggggaggtcctgagtttgtgcag
aggcgaggctgagaggggaggtccctaagtgcaggggtgaggccgagaggggaggttg
caaatttgtgcaggggtgaggccaagaggggaggtcctgagtt"
/db_xref="dbSNP:1950675161"
variation 3891
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2136902583"
variation 3892
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="g"
/db_xref="dbSNP:1950677006"
variation 3893
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:2543260897"
variation 3894
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:2136902575"
variation 3897..3965
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="ggtgcaggggtgagggagaggggaggtcctgagtttgtgcagaggcga
ggctgagaggggaggtcccta"
/db_xref="dbSNP:2543260624"
variation 3897
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1318829314"
variation 3898
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:146473933"
variation 3900
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:573757831"
variation 3901
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1950676905"
variation 3902
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1376745696"
variation 3903
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2136902556"
variation 3904
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1950676869"
variation 3906
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1950676853"
variation 3907
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1317131032"
variation 3908..3918
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="gaggg"
/replace="gagggagaggg"
/db_xref="dbSNP:1448687386"
variation 3909
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2136902542"
variation 3911..3912
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="cc"
/replace="ct"
/db_xref="dbSNP:1410612498"
variation 3911
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:987168605"
variation 3912..3962
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="gagaggggaggtcc"
/replace="gagaggggaggtcctgagtttgtgcagaggcgaggctgagaggggagg
tcc"
/db_xref="dbSNP:2543260641"
variation 3912
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:534014192"
variation 3913
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:2136902518"
variation 3915
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="a"
/db_xref="dbSNP:1298285389"
variation 3916..3917
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="ca"
/db_xref="dbSNP:1950676726"
variation 3917
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:2543260774"
variation 3918
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1683942538"
variation 3920
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:2543260756"
variation 3922
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:540537253"
variation 3923
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1269174524"
variation 3924
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1328684765"
variation 3925
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1229889316"
variation 3926
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1466769906"
variation 3927
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950676602"
variation 3928
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:2543260731"
variation 3932
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:1400510999"
variation 3933
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1950676568"
variation 3936
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950676555"
variation 3937
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1240700253"
variation 3938
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1288293843"
variation 3939
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="a"
/db_xref="dbSNP:2543260714"
variation 3939
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1163671172"
variation 3940
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2543260707"
variation 3941
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1593434959"
variation 3942
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1422364269"
variation 3943
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1238311304"
variation 3944
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1593434947"
variation 3949..3953
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="gag"
/replace="gagag"
/db_xref="dbSNP:1484355663"
variation 3949
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2136902416"
variation 3951..3952
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="c"
/db_xref="dbSNP:2543260690"
variation 3952
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="a"
/db_xref="dbSNP:1950676403"
variation 3952
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="aa"
/db_xref="dbSNP:1950676389"
variation 3952
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1950676366"
variation 3953..3956
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="gggg"
/replace="ggggg"
/db_xref="dbSNP:1950676277"
variation 3953
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1950676337"
variation 3954
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950676316"
variation 3955
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1180533723"
variation 3958
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1190190262"
variation 3959
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1440847228"
variation 3960
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:2543260654"
variation 3961
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950676221"
variation 3962
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1593434933"
variation 3963..3964
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="atg"
/replace="gagtt"
/replace="gtg"
/db_xref="dbSNP:1950676165"
variation 3963
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1160931747"
variation 3964..3965
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="ta"
/replace="tagta"
/db_xref="dbSNP:2543260621"
variation 3964
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1950676147"
variation 3965..3966
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="gtt"
/db_xref="dbSNP:1416423908"
variation 3965..3966
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="aa"
/db_xref="dbSNP:2543260613"
variation 3965..3966
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="aa"
/db_xref="dbSNP:1950676100"
variation 3965
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:1950676129"
variation 3966..3967
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="ttt"
/db_xref="dbSNP:1950676079"
variation 3967..4019
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="gtgcaggggtgaggcc"
/replace="gtgcaggggtgaggccgagaggggaggttgcaaatttgtgcaggggtg
aggcc"
/replace="gtgcaggggtgaggccgagaggggaggttgcaaatttgtgcaggggtg
aggccgagaggggaggttgcaaatttgtgcaggggtgaggcc"
/db_xref="dbSNP:1950675595"
variation 3967
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950676059"
variation 3969
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1182861753"
variation 3971
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:955411091"
variation 3972..4068
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="ggggtgaggccgagaggggaggt"
/replace="ggggtgaggccgagaggggaggttgcaaatttgtgcaggggtgaggcc
aagaggggaggtcctgagttagtgcgggggtgaggccgagaggggaggt"
/db_xref="dbSNP:1566169391"
variation 3972
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2543260485"
variation 3974
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950676022"
variation 3975
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950675998"
variation 3976
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1316977979"
variation 3978
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2543260462"
variation 3979
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950675954"
variation 3980
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1359442719"
variation 3982
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1439615312"
variation 3983..3987
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="gag"
/replace="gagag"
/db_xref="dbSNP:1236924109"
variation 3983
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:533877400"
variation 3984
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2543260445"
variation 3986
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1593434916"
variation 3987
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950675858"
variation 3988
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950675840"
variation 3989
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1180566500"
variation 3990
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950675803"
variation 3993..4000
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="gttgcaaa"
/db_xref="dbSNP:2543260420"
variation 3993
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1950675784"
variation 3994
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1348419019"
variation 3995
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1593434903"
variation 3996
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1593434899"
variation 3997..4003
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="caaattt"
/db_xref="dbSNP:1950675664"
variation 3999
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950675715"
variation 4000
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1458291288"
variation 4001..4246
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="tttgtgcaggggtgaggccaagaggggaggtcctgagttagtgcgggg
gtgaggccgagaggggag"
/replace="tttgtgcaggggtgaggccaagaggggaggtcctgagttagtgcgggg
gtgaggccgagaggggaggtcctgagtttgtgcagaggcgaggctgagaggggaggtc
cttagtgcaggggtgaggctgagagggggaggtcccaagtttgtgcaggggtgaggcc
gaggggaggttgcaagtttgtgcaggggtgaggccaagaggggaggtcctgagttagt
gcgggggtgaggccgagaggggag"
/db_xref="dbSNP:1950671843"
variation 4003
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:2543260140"
variation 4009
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2543260137"
variation 4013
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1279403593"
variation 4015
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2543260131"
variation 4018
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:2543260128"
variation 4019..4020
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="ca"
/db_xref="dbSNP:2543260114"
variation 4019
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1265047653"
variation 4020..4021
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="aa"
/db_xref="dbSNP:1950675512"
variation 4020..4021
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="aa"
/db_xref="dbSNP:1950675492"
variation 4020
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1314175824"
variation 4021..4076
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="agaggggaggtcctgagtt"
/replace="agaggggaggtcctgagttagtgcgggggtgaggccgagaggggaggt
cctgagtt"
/db_xref="dbSNP:1950674266"
variation 4021
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2543260098"
variation 4022
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1208198011"
variation 4023
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="a"
/db_xref="dbSNP:2136902231"
variation 4024..4027
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="gggg"
/replace="ggggg"
/db_xref="dbSNP:1458457254"
variation 4024..4025
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="ca"
/db_xref="dbSNP:2543260088"
variation 4024
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1593434882"
variation 4025
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:918640529"
variation 4027
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1950675342"
variation 4029
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1593434876"
variation 4030
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2543260079"
variation 4031
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1950675299"
variation 4032..4041
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="cctgagttag"
/db_xref="dbSNP:1950675094"
variation 4032
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1180874604"
variation 4033
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1593434867"
variation 4034
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1219656801"
variation 4035..4036
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="ca"
/db_xref="dbSNP:1950675211"
variation 4035
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1319641468"
variation 4036..4042
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="agt"
/replace="agttagt"
/db_xref="dbSNP:1950675047"
variation 4036
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:2136902182"
variation 4037
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1950675197"
variation 4038
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:1157498980"
variation 4039
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1950675142"
variation 4040
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1291745659"
variation 4041
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950675069"
variation 4044
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1415853224"
variation 4045..4064
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="gggggtgaggccgagagggg"
/db_xref="dbSNP:1950674551"
variation 4045..4049
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="gggg"
/replace="ggggg"
/replace="gggggg"
/db_xref="dbSNP:1333964449"
variation 4045
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:59036121"
variation 4046
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1404878482"
variation 4047
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1376022691"
variation 4049
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1333117363"
variation 4050
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1441314678"
variation 4051..4092
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="gaggccgagaggggaggtcctgagtttgtgcagaggcgaggc"
/replace="gaggccgagaggggaggtcctgagtttgtgcagaggcgaggccgagag
gggaggtcctgagtttgtgcagaggcgaggc"
/db_xref="dbSNP:2543259923"
variation 4051
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950674830"
variation 4052
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2543260015"
variation 4053
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1275513725"
variation 4055..4056
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="cc"
/db_xref="dbSNP:1950674783"
variation 4056
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1307019957"
variation 4057..4061
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="gag"
/replace="gagag"
/db_xref="dbSNP:1318830997"
variation 4057
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1221935495"
variation 4058
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1448297550"
variation 4060
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="aa"
/db_xref="dbSNP:1950674664"
variation 4060
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:2136902097"
variation 4061..4064
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="gggg"
/replace="ggggg"
/db_xref="dbSNP:1950674522"
variation 4061
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950674609"
variation 4062
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1200988270"
variation 4064
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1593434802"
variation 4066..4072
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="ggtcctg"
/db_xref="dbSNP:1950674301"
variation 4066
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950674478"
variation 4067
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1377000379"
variation 4068..4285
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="tcctgagtttgtgcagaggcgaggctgagaggggaggt"
/replace="tcctgagtttgtgcagaggcgaggctgagaggggaggtccttagtgca
ggggtgaggctgagagggggaggtcccaagtttgtgcaggggtgaggccgaggggagg
ttgcaagtttgtgcaggggtgaggccaagaggggaggtcctgagttagtgcgggggtg
aggccgagaggggagttcctgagtttgtgcagaggcgaggctgagaggggaggt"
/db_xref="dbSNP:2543259463"
variation 4069
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950674392"
variation 4070
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950674365"
variation 4071
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1292522956"
variation 4072
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1593434793"
variation 4077
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:1456049142"
variation 4080
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1200150075"
variation 4081
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2543259945"
variation 4082..4099
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="agagg"
/replace="agaggcgaggctgagagg"
/db_xref="dbSNP:2543259909"
variation 4082
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950674211"
variation 4083
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2543259940"
variation 4084
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:551161492"
variation 4087
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1478755130"
variation 4088
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950674119"
variation 4089
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2543259931"
variation 4091
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1566169380"
variation 4093
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1196615271"
variation 4094..4098
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="gag"
/replace="gagag"
/db_xref="dbSNP:2543259912"
variation 4094
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1428251879"
variation 4097
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="a"
/db_xref="dbSNP:2543259920"
variation 4097
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="aa"
/db_xref="dbSNP:2543259917"
variation 4097
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1593434772"
variation 4098..4101
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="ggg"
/replace="gggg"
/db_xref="dbSNP:1950673966"
variation 4098
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1465808749"
variation 4103
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950673936"
variation 4104
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1950673909"
variation 4105
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1593434768"
variation 4106
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:2136901986"
variation 4107..4108
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="caag"
/replace="cgag"
/replace="cgtg"
/replace="ctag"
/replace="ggag"
/db_xref="dbSNP:rs1950673795"
variation 4107
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1950673828"
variation 4108
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1593434763"
variation 4108
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="t"
/replace="tgagt"
/db_xref="dbSNP:2543259891"
variation 4109
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1950673742"
variation 4110
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="aa"
/db_xref="dbSNP:1593434760"
variation 4110
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:1172569152"
variation 4111
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2543259882"
variation 4115
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1593434755"
variation 4116
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950673652"
variation 4118
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1393975699"
variation 4119
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:533049613"
variation 4120
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1419529037"
variation 4121
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:557336198"
variation 4122
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1593434740"
variation 4124
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:972863275"
variation 4125
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1950673455"
variation 4126
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1593434734"
variation 4127..4131
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="gag"
/replace="gagag"
/db_xref="dbSNP:1268819461"
variation 4127
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="g"
/db_xref="dbSNP:2136901914"
variation 4128
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2543259852"
variation 4129..4139
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="gagggggaggt"
/db_xref="dbSNP:1950673245"
variation 4129..4132
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="gagg"
/db_xref="dbSNP:1950673366"
variation 4129
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="g"
/db_xref="dbSNP:2136901910"
variation 4129
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1220626370"
variation 4130
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="a"
/db_xref="dbSNP:1950673399"
variation 4131..4135
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="gggg"
/replace="ggggg"
/replace="gggggg"
/db_xref="dbSNP:1210790352"
variation 4131
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2136901892"
variation 4135
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1440328813"
variation 4136
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1593434723"
variation 4137
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1950673279"
variation 4138
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1593434721"
variation 4139
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1950673231"
variation 4140
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1292696118"
variation 4141
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1490002407"
variation 4142..4199
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="caagtttgtgcaggggtgaggcc"
/replace="caagtttgtgcaggggtgaggccgaggggaggttgcaagtttgtgcag
gggtgaggcc"
/db_xref="dbSNP:1950672632"
variation 4143
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1593434710"
variation 4144
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:2543259813"
variation 4145
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950673167"
variation 4148
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:1593434706"
variation 4149
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1219697025"
variation 4154
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:2136901850"
variation 4155
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1267479516"
variation 4156
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1477944783"
variation 4157
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2136901840"
variation 4158
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2543259796"
variation 4159
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1195341655"
variation 4160
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1593434694"
variation 4161..4165
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="ggccg"
/db_xref="dbSNP:1950673007"
variation 4161
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2136901833"
variation 4162
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950673054"
variation 4163..4164
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="cc"
/db_xref="dbSNP:2136901824"
variation 4164..4192
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="cgaggggaggttgcaagtttgtgcagggg"
/db_xref="dbSNP:2543259725"
variation 4164
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:539019801"
variation 4165..4288
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="gaggggaggttgc"
/replace="gaggggaggttgcaagtttgtgcaggggtgaggccaagaggggaggtc
ctgagttagtgcgggggtgaggccgagaggggagttcctgagtttgtgcagaggcgag
gctgagaggggaggttgc"
/db_xref="dbSNP:2543259447"
variation 4165..4167
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="gag"
/replace="gagag"
/db_xref="dbSNP:1489586238"
variation 4165
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1189606159"
variation 4166
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="aaa"
/db_xref="dbSNP:2136901813"
variation 4167..4170
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="gggg"
/replace="ggggg"
/db_xref="dbSNP:1163590651"
variation 4167..4168
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="aa"
/replace="ca"
/db_xref="dbSNP:2543259769"
variation 4173
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1247553086"
variation 4175
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1392874465"
variation 4176
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:2136901796"
variation 4177
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1950672904"
variation 4178..4179
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="gagaccctg"
/db_xref="dbSNP:2543259749"
variation 4178
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:2136901787"
variation 4179
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:961855476"
variation 4180
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1352754472"
variation 4181..4183
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="ttt"
/db_xref="dbSNP:2543259738"
variation 4183
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:2543259735"
variation 4184
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950672827"
variation 4188
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1361205708"
variation 4189..4236
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="ggggtgaggcc"
/replace="ggggtgaggccaagaggggaggtcctgagttagtgcgggggtgaggcc
"
/db_xref="dbSNP:1950671995"
variation 4189..4192
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="gggg"
/replace="ggggg"
/db_xref="dbSNP:2543259723"
variation 4189
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1950672787"
variation 4190
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1950672762"
variation 4191
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1016134331"
variation 4192
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1950672727"
variation 4193
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1950672714"
variation 4194
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950672697"
variation 4195
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2543259715"
variation 4197..4198
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="gc"
/db_xref="dbSNP:2543259684"
variation 4197
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1950672677"
variation 4198..4236
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="ccaagaggggaggtcctgagttagtgcgggggtgaggcc"
/db_xref="dbSNP:2543259568"
variation 4198
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1283712461"
variation 4199..4200
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="ca"
/db_xref="dbSNP:2136901743"
variation 4199
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1242241448"
variation 4200..4201
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="aa"
/db_xref="dbSNP:2543259664"
variation 4200
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1326048176"
variation 4201..4204
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="agag"
/db_xref="dbSNP:2543259656"
variation 4201..4204
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="ag"
/replace="agag"
/db_xref="dbSNP:1299979347"
variation 4201
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2543259662"
variation 4203
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="a"
/db_xref="dbSNP:2543259658"
variation 4204..4207
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="ggg"
/replace="gggg"
/replace="ggggg"
/db_xref="dbSNP:1286311811"
variation 4204..4205
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="ca"
/db_xref="dbSNP:2543259648"
variation 4204
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1354394467"
variation 4207
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2543259645"
variation 4209
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1384607504"
variation 4211..4256
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="tcctgagttagtgcgggggtgaggccgagaggggagttcctgagtt"
/replace="tcctgagttagtgcgggggtgaggccgagaggggagttcctgagttag
tgcgggggtgaggccgagaggggagttcctgagtt"
/db_xref="dbSNP:1950671733"
variation 4211
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1593434643"
variation 4212
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950672446"
variation 4213..4249
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="ctgagttagtgcgggggtgaggccgagaggggagttc"
/db_xref="dbSNP:2543259536"
variation 4213
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1369255281"
variation 4214..4218
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="t"
/replace="tgagt"
/db_xref="dbSNP:2543259624"
variation 4214
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:2136901722"
variation 4215
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:2136901720"
variation 4216
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:2543259631"
variation 4217
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1293776851"
variation 4219
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950672400"
variation 4220
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1399742668"
variation 4221..4261
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="gtgc"
/replace="gtgcgggggtgaggccgagaggggagttcctgagtttgtgc"
/db_xref="dbSNP:2543259509"
variation 4223..4228
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="gcgggg"
/db_xref="dbSNP:1950672195"
variation 4223
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950672335"
variation 4224
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1359038245"
variation 4225..4239
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="gggggtgaggccgag"
/db_xref="dbSNP:2136901637"
variation 4225..4229
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="gggg"
/replace="ggggg"
/db_xref="dbSNP:1950672153"
variation 4225
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1034174540"
variation 4227
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:760290"
variation 4228
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1206357308"
variation 4229
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1259280928"
variation 4230
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1420827353"
variation 4231
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950672050"
variation 4232
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:888282078"
variation 4234..4235
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="gc"
/db_xref="dbSNP:1950672011"
variation 4234
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:2136901662"
variation 4235..4236
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="cc"
/db_xref="dbSNP:1293783486"
variation 4235..4236
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="cc"
/db_xref="dbSNP:1006135819"
variation 4236
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1188065644"
variation 4237..4283
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="gagaggggag"
/replace="gagaggggagttcctgagtttgtgcagaggcgaggctgagaggggag"
/db_xref="dbSNP:1950671519"
variation 4237..4241
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="gag"
/replace="gagag"
/db_xref="dbSNP:1174007358"
variation 4237
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1442738081"
variation 4238
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1162800549"
variation 4240
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="aa"
/db_xref="dbSNP:2543259557"
variation 4240
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:2136901635"
variation 4241
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2136901629"
variation 4243..4266
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="gg"
/replace="ggagttcctgagtttgtgcagagg"
/db_xref="dbSNP:2543259494"
variation 4244
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1950671867"
variation 4247
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:879410312"
variation 4248
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1435030866"
variation 4249..4250
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="cc"
/db_xref="dbSNP:1426083991"
variation 4249
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1950671784"
variation 4250
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2543259531"
variation 4251
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="t"
/db_xref="dbSNP:2543259529"
variation 4251
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:2136901599"
variation 4252
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2543259518"
variation 4253
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950671758"
variation 4257
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:1950671716"
variation 4260
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:753905691"
variation 4261
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2543259505"
variation 4262
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950671678"
variation 4263
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2543259497"
variation 4264
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1384599528"
variation 4266..4321
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="gcgaggctgagaggggagg"
/replace="gcgaggctgagaggggaggttgccagtttgtgcaggtgcgaggctgag
aggggagg"
/db_xref="dbSNP:1283455357"
variation 4267
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:115482424"
variation 4268
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:538087058"
variation 4269
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2543259485"
variation 4272
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:897799162"
variation 4273
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1950671607"
variation 4274..4278
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="gag"
/replace="gagag"
/db_xref="dbSNP:1336559145"
variation 4277
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="aa"
/db_xref="dbSNP:2543259477"
variation 4277
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:2543259476"
variation 4278
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2543259473"
variation 4279
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1260746049"
variation 4281..4303
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="gaggttgccagtttgtgcaggtg"
/db_xref="dbSNP:2543259406"
variation 4281
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1023559578"
variation 4284
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2136901554"
variation 4285
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1593434561"
variation 4286..4287
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="tg"
/db_xref="dbSNP:2136901550"
variation 4286
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2543259455"
variation 4286
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="t"
/replace="tct"
/db_xref="dbSNP:2543259460"
variation 4287
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:2543259450"
variation 4288..4289
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="cc"
/db_xref="dbSNP:2543259443"
variation 4289..4290
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="ca"
/replace="cg"
/replace="cta"
/replace="g"
/db_xref="dbSNP:rs2136901546"
variation 4291..4296
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="gt"
/replace="gtttgt"
/db_xref="dbSNP:2543259431"
variation 4291
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1310687810"
variation 4293
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:2543259433"
variation 4294..4297
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="tg"
/replace="tgtg"
/db_xref="dbSNP:773514601"
variation 4294
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:2136901537"
variation 4296
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:114830287"
variation 4298
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="c"
/db_xref="dbSNP:2543259416"
variation 4298
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2543259415"
variation 4302
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1258417521"
variation 4304
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1349518248"
variation 4305
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:879680270"
variation 4306
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950671377"
variation 4307
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:944940871"
variation 4311..4315
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="gag"
/replace="gagag"
/db_xref="dbSNP:1682846501"
variation 4311
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:2543259392"
variation 4314
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="aa"
/db_xref="dbSNP:2543259386"
variation 4315
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1950671340"
variation 4317
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1244772415"
variation 4321
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1313476649"
variation 4330
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:185106633"
variation 4331
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:149983112"
variation 4332
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1593434527"
variation 4334
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:2136901477"
variation 4335
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1157033776"
variation 4339
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1363235316"
variation 4340
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1593434516"
variation 4344
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2136901464"
variation 4347
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950671154"
variation 4354
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1466770465"
variation 4356
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1174483648"
variation 4359
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:75850993"
variation 4360
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1401035351"
variation 4361..4363
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="t"
/replace="tct"
/db_xref="dbSNP:2543259334"
variation 4362
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1332452920"
variation 4365
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:2543259331"
variation 4368
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1950671026"
variation 4369..4370
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="tt"
/db_xref="dbSNP:2543259324"
variation 4370
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950671009"
variation 4371..4377
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="aga"
/replace="agagaga"
/db_xref="dbSNP:546713382"
variation 4371
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="aa"
/db_xref="dbSNP:1402095148"
variation 4371
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950670964"
variation 4373
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1390109583"
variation 4377
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1304233997"
variation 4378
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:926136213"
variation 4379
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1467589437"
variation 4380
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1320972360"
variation 4384
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1593434465"
variation 4387..4394
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="actc"
/replace="actcactc"
/db_xref="dbSNP:1950670811"
variation 4388
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:977550932"
variation 4390
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:767662065"
variation 4398
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1950670792"
variation 4399
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1359827174"
variation 4400
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1258408575"
variation 4403
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:904020201"
variation 4404
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:967177707"
variation 4405
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950670720"
variation 4406
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:916888296"
variation 4408
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1175367086"
variation 4410
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1043909610"
variation 4416
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950670636"
variation 4418
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1433891462"
variation 4419
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:942872747"
variation 4421..4423
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="aaa"
/replace="aaaa"
/db_xref="dbSNP:1950670592"
variation 4424
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:992538650"
variation 4427
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1480223893"
variation 4430
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950670542"
variation 4431
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1171847444"
variation 4432
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="c"
/db_xref="dbSNP:1051366099"
variation 4432
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:79091287"
variation 4433
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950670468"
variation 4435
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950670451"
variation 4438
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1298155520"
variation 4441
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:1566169107"
variation 4442
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:933964127"
variation 4443
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2543259256"
variation 4447
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1386916818"
variation 4449
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1284634327"
variation 4450
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950670362"
variation 4456..4458
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="ttt"
/replace="tttt"
/db_xref="dbSNP:1391346519"
variation 4461
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:533347982"
variation 4463
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950670314"
variation 4468
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1343274450"
variation 4469
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:918622061"
variation 4474
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950670251"
variation 4476
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1034228365"
variation 4477
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:941460149"
variation 4482
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950670137"
variation 4484
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950670122"
variation 4485
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1428918922"
variation 4486
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:751911378"
variation 4488
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:562666893"
variation 4491
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950670047"
variation 4492
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1566169073"
variation 4495
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1483915895"
variation 4498
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1950669999"
variation 4501..4506
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="ag"
/replace="agag"
/replace="agagag"
/db_xref="dbSNP:1950669923"
variation 4501
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1263207873"
variation 4502
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:544491093"
variation 4505
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:952496090"
variation 4507
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:2543259191"
variation 4510
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:984585236"
variation 4511
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:2136901229"
variation 4512
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1197532742"
variation 4514
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1593434338"
variation 4518
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1315650857"
variation 4520
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1480235247"
variation 4521
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1025502443"
variation 4522
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1593434322"
variation 4525
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950669767"
variation 4533
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1279754561"
variation 4538..4549
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="tcctgcttcctt"
/replace="tcctgcttcctttcctgcttcctt"
/db_xref="dbSNP:1228554287"
variation 4539
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1421889876"
variation 4542
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:2136901197"
variation 4545
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950669723"
variation 4546
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1427150820"
variation 4547
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1170185669"
variation 4553
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950669649"
variation 4557
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1593434300"
variation 4560
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:561272589"
variation 4567
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1427046283"
variation 4568..4569
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="ctgtggcccactgtgaagaggatttctcttcac"
/db_xref="dbSNP:1304440762"
variation 4568..4569
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="aa"
/db_xref="dbSNP:1950669553"
variation 4569
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:764656153"
variation 4570
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950669514"
variation 4572..4573
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="cc"
/db_xref="dbSNP:1298479999"
variation 4572
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1403974116"
variation 4573
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:897938058"
variation 4575
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1363593177"
variation 4576
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:992112257"
variation 4577
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1311130846"
variation 4580
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1322269082"
variation 4583
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:747672649"
variation 4584
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:763423700"
variation 4586
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1950669350"
variation 4587
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1950669333"
variation 4588
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1950669319"
variation 4589
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:1950669301"
variation 4591
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1566168993"
variation 4593
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:1407556289"
variation 4594..4601
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="t"
/replace="ttctacct"
/db_xref="dbSNP:1950669191"
variation 4596
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950669250"
variation 4598
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:573795105"
variation 4599
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1217393564"
variation 4600
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:561929414"
variation 4603
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:889119182"
variation 4606
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950669165"
variation 4607
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1950669146"
variation 4610
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:960638758"
variation 4611
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1464173934"
variation 4615
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1950669103"
variation 4616
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1950669088"
variation 4617
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1030698389"
variation 4618
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:140647039"
variation 4623
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1162174725"
variation 4629
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1385130212"
variation 4630
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950668992"
variation 4638
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:903571906"
variation 4639
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:1950668960"
variation 4642
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1367694666"
variation 4645
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950668921"
variation 4648
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1950668904"
variation 4650
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1022010021"
variation 4653
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1428143702"
variation 4660
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1288074825"
variation 4662
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:936273874"
variation 4665
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950668851"
variation 4666..4667
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="ga"
/db_xref="dbSNP:1950668835"
variation 4668
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1185224037"
variation 4669
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:572626236"
variation 4671
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1006985916"
variation 4673
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950668763"
variation 4674
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1241038347"
variation 4675
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:904679113"
variation 4678
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1286363295"
variation 4679..4747
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="gtggtaaggagccgtgttttatggaggcagggagatcagggcagttac
tcctcgggtgtggtaaggagc"
/replace="gtggtaaggagccgtgttttatggaggcagggagatcagggcagttac
tcctcgggtgtggtaaggagccgtgttttatggaggcagggagatcagggcagttact
cctcgggtgtggtaaggagc"
/db_xref="dbSNP:1950668050"
variation 4679
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1041915475"
variation 4681
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2543258904"
variation 4682
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1462972086"
variation 4686
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1456086661"
variation 4688
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1051765251"
variation 4691
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:369500865"
variation 4692..4760
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="gtgttttatgga"
/replace="gtgttttatggaggcagggagatcagggcagttactcctcgggtgtgg
taaggagctgtgttttatgga"
/replace="gtgttttatggaggcagggagatcagggcagttactcctcgggtgtgg
taaggagctgtgttttatggaggcagggagatcagggcagttactcctcgggtgtggt
aaggagctgtgttttatgga"
/db_xref="dbSNP:1950667953"
variation 4692
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1259546719"
variation 4693
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1196028133"
variation 4695
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:945778666"
variation 4698
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1398626160"
variation 4702
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950668500"
variation 4704
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1355276417"
variation 4708
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1264044106"
variation 4715
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:917044204"
variation 4716
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1950668429"
variation 4717
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950668405"
variation 4719
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1950668388"
variation 4722
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1334434312"
variation 4723
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:897142595"
variation 4725
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950668330"
variation 4726..4731
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="ctc"
/replace="ctcctc"
/db_xref="dbSNP:1593434128"
variation 4726
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1442757448"
variation 4728
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:557398453"
variation 4731
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1371218105"
variation 4732
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:936955964"
variation 4733
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1325917210"
variation 4734
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:980199228"
variation 4737
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1458609234"
variation 4741
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1207191835"
variation 4744
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1309195509"
variation 4745
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1234136551"
variation 4747
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950668037"
variation 4748
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1468199593"
variation 4749
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1444602239"
variation 4751
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:539082548"
variation 4761
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1176119452"
variation 4766
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:926959878"
variation 4767
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1593434093"
variation 4768..4769
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="gg"
/replace="gggg"
/db_xref="dbSNP:1950667880"
variation 4768
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2543258812"
variation 4770
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:984015869"
variation 4771
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:952631374"
variation 4772
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:575159074"
variation 4774
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2136900854"
variation 4779
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1405035822"
variation 4782
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:1950667787"
variation 4783
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1410488828"
variation 4784
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950667735"
variation 4785
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:556622412"
variation 4786
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2136900837"
variation 4787
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1352656818"
variation 4788
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1950667641"
variation 4789
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950667618"
variation 4793
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1030877756"
variation 4794
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1950667551"
variation 4798..4802
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="ct"
/replace="cttct"
/db_xref="dbSNP:1566168823"
variation 4799
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:1347634260"
variation 4800
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1566168827"
variation 4801
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1221841193"
variation 4803
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950667445"
variation 4806
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:977692798"
variation 4807
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1459294944"
variation 4809..4810
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="cc"
/db_xref="dbSNP:1216669249"
variation 4812
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:972628351"
variation 4813
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1437745717"
variation 4815
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:967701427"
variation 4819
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1490748227"
variation 4820
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950667227"
variation 4824
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1021977739"
variation 4825
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1593434048"
variation 4827
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="g"
/db_xref="dbSNP:1950667156"
variation 4832
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1428143225"
variation 4835
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1950667110"
variation 4836
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:962438637"
variation 4838
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1169420478"
variation 4839
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1018992203"
variation 4840
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1409239092"
variation 4847
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1239453577"
variation 4850
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:538537557"
variation 4851
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:889938997"
variation 4852
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:567824791"
variation 4853
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:549572537"
variation 4856
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="gggggggggg"
/db_xref="dbSNP:147170344"
variation 4857
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1593434015"
variation 4859
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1327217809"
variation 4860
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1593434008"
variation 4863
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1593434007"
variation 4867
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950666596"
variation 4870
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:889091445"
variation 4871
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:534364366"
variation 4873
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1339313457"
variation 4883
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950666494"
variation 4886
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1950666462"
variation 4887
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1950666436"
variation 4889
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:180799952"
variation 4892
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1000389331"
variation 4894
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1361039752"
variation 4896
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:904815256"
variation 4897
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1042275688"
variation 4903
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1329540776"
variation 4904
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:374919773"
variation 4906
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950666176"
variation 4912
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950666158"
variation 4917
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1566168725"
variation 4919
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:772928565"
variation 4920
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1950666088"
variation 4922
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1950666066"
variation 4923
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1950666049"
variation 4926
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:1195073314"
variation 4934
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1950666009"
variation 4935..4954
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="ctgctgcagatcccactgct"
/replace="ctgctgcagatcccactgctgcagatcccactgct"
/db_xref="dbSNP:1386988924"
variation 4935
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1950665986"
variation 4940
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:551890669"
variation 4946
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:916396641"
variation 4948
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950665932"
variation 4950
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950665909"
variation 4953..4959
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="cttc"
/replace="cttcttc"
/db_xref="dbSNP:939188387"
variation 4955
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:533407229"
variation 4956
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1422865411"
variation 4960
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1385963870"
variation 4963
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1384072824"
variation 4967
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:923831840"
variation 4972..4974
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="ccc"
/replace="cccc"
/db_xref="dbSNP:1297413435"
variation 4973
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1950665733"
variation 4974
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1326167244"
variation 4979
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1950665663"
variation 4981..4995
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="ggg"
/replace="gggacaaacccaggg"
/db_xref="dbSNP:1950665531"
variation 4981
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:2136900595"
variation 4982
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:977998360"
variation 4983..4988
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="gacaaa"
/db_xref="dbSNP:1950665615"
variation 4983
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1317829535"
variation 4989..4991
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="cc"
/replace="ccc"
/db_xref="dbSNP:2543258600"
variation 4991..5006
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="cag"
/replace="cagggcagggctgcag"
/db_xref="dbSNP:1950665437"
variation 4991
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1381226158"
variation 4992
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:1950665566"
variation 4993
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1950665550"
variation 4996
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950665510"
variation 4997..5048
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="agggctgcagctgcccgctggccccacagaccgtctccccacgcactc
ctca"
/db_xref="dbSNP:1950664991"
variation 5000
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1243209945"
variation 5001
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:967670302"
variation 5002
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1350946834"
variation 5009
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2543258575"
variation 5010
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950665421"
variation 5012
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:895978937"
variation 5013
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:771835001"
variation 5014
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2136900540"
variation 5018
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:748022175"
variation 5019
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950665335"
variation 5020
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950665305"
variation 5023
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:914937623"
variation 5024
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2136900522"
variation 5025
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:937093380"
variation 5027
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950665236"
variation 5028
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:778819563"
variation 5029
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:983817015"
variation 5034
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950665188"
variation 5035
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:142419835"
variation 5037
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:1200550878"
variation 5038
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1029830644"
variation 5039
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:998331954"
variation 5039
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="gg"
/db_xref="dbSNP:1950665126"
variation 5040
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:563852447"
variation 5041
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:768762435"
variation 5042..5047
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="ctc"
/replace="ctcctc"
/db_xref="dbSNP:1470548103"
variation 5044
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1950665048"
variation 5046
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2543258529"
variation 5047
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1489541667"
variation 5049
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1531822"
variation 5050
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1218672691"
variation 5052
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:561799412"
variation 5053
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:779817479"
variation 5054
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:189502291"
variation 5056
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1224340841"
variation 5058
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1311425495"
variation 5059
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950664833"
variation 5060
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:572677363"
variation 5062
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1240533457"
variation 5063
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="t"
/replace="tt"
/db_xref="dbSNP:1950664782"
variation 5064
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="g"
/db_xref="dbSNP:1950664767"
variation 5067
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:563870607"
variation 5069
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1328043652"
variation 5071
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950664723"
variation 5074
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950664702"
variation 5076
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1204074053"
variation 5080
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:756224376"
variation 5082
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1418885536"
variation 5083
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950664629"
variation 5086
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:1340204503"
variation 5088
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:888439464"
variation 5089
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1397965314"
variation 5091
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:779960536"
variation 5093
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1421003932"
variation 5094
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="t"
/db_xref="dbSNP:1950664516"
variation 5094
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1593433824"
variation 5095
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:750414604"
variation 5096
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950664473"
variation 5097
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1179748877"
variation 5099
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1044454500"
variation 5100
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2543258441"
variation 5102
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950664424"
variation 5105
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:545482117"
variation 5106
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1593433812"
variation 5108
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950664372"
variation 5109
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1013336232"
variation 5113
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1404317356"
variation 5114
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:575175027"
variation 5116
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:184615275"
variation 5123
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1593433797"
variation 5127
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1950664265"
variation 5130
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1178042354"
variation 5131
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:145974609"
variation 5134
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2543258411"
variation 5135
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:939175820"
variation 5140
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950664205"
variation 5143
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1950664182"
variation 5146
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1566168564"
variation 5147
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1000192109"
variation 5151
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:757469324"
variation 5152
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950664121"
variation 5156
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1223703095"
variation 5161
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1284981312"
variation 5164..5165
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="aa"
/db_xref="dbSNP:1321216147"
variation 5166..5168
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="cc"
/replace="ccc"
/db_xref="dbSNP:1194161542"
variation 5167
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1020500401"
variation 5168
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:758126953"
variation 5169
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1251092684"
variation 5170
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1210038125"
variation 5171..5172
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="cc"
/db_xref="dbSNP:2543258374"
variation 5172
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1490584731"
variation 5174
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1440717355"
variation 5175
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:895962801"
variation 5178
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:946669790"
variation 5181
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1057489758"
variation 5184
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1433010671"
variation 5185
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1171559838"
variation 5186
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1001272519"
variation 5188
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:905645385"
variation 5190
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:574298767"
variation 5198
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:2543258349"
variation 5199
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1305672012"
variation 5200..5203
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="ct"
/replace="ctct"
/db_xref="dbSNP:2543258345"
variation 5201
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950663837"
variation 5202
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1369348163"
variation 5208
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:556075693"
variation 5214
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950663787"
variation 5218
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1950663770"
variation 5221
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:953854235"
variation 5228
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1343247476"
variation 5230
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2543258329"
variation 5232
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2136900227"
variation 5234..5235
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="tg"
/db_xref="dbSNP:1950663723"
variation 5234
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:534429537"
variation 5236
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950663710"
variation 5238..5256
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="caga"
/replace="cagattggcttaaaacaga"
/db_xref="dbSNP:1950663597"
variation 5238
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950663701"
variation 5240
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950663687"
variation 5241
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:930928646"
variation 5243
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1295950917"
variation 5247
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:1950663652"
variation 5248
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2543258318"
variation 5249
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950663635"
variation 5255
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:922349468"
variation 5256
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:1950663583"
variation 5258..5259
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="tg"
/db_xref="dbSNP:1274044835"
variation 5258..5259
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="tg"
/replace="tgtg"
/db_xref="dbSNP:1950663551"
variation 5259
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1225107842"
variation 5262
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950663523"
variation 5263
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:112406395"
variation 5267
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950663486"
variation 5268
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950663470"
variation 5270
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1216523245"
variation 5271
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1669635299"
variation 5273
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:558331174"
variation 5275
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:751964773"
variation 5276
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:545133440"
variation 5278
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2543258292"
variation 5280
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:375709552"
variation 5284
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950663353"
variation 5288
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1187485140"
variation 5290
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1015802250"
variation 5291
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:539942905"
variation 5296
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1168564590"
variation 5298
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950663258"
variation 5301
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950663238"
variation 5304
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1950663221"
variation 5305
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:952901056"
variation 5307
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:985291853"
variation 5312
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1424818364"
variation 5313
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1950663152"
variation 5316
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2136900135"
variation 5324
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1950663135"
variation 5325
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1023646170"
variation 5329..5332
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="t"
/replace="taat"
/db_xref="dbSNP:1012889898"
variation 5333
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950663056"
variation 5335
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:569212309"
variation 5336
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:764460239"
variation 5337..5362
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="tcagggccagcaggatgggagtggtc"
/replace="tcagggccagcaggatgggagtggtcagggccagcaggatgggagtgg
tc"
/db_xref="dbSNP:1950662906"
variation 5341
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:921980319"
variation 5343
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950662979"
variation 5344
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950662966"
variation 5347
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:978822629"
variation 5349
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1296838710"
variation 5353..5355
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="gg"
/replace="ggg"
/db_xref="dbSNP:1566168458"
variation 5354
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2543258236"
variation 5356
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1950662922"
variation 5362
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950662886"
variation 5363
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:968718991"
variation 5369
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:998925173"
variation 5371
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1020722382"
variation 5377
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1010470578"
variation 5380
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950662792"
variation 5381
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950662779"
variation 5382..5385
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="gggg"
/replace="ggggg"
/db_xref="dbSNP:1042243774"
variation 5382
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:960597990"
variation 5383
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1262689766"
variation 5384
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1485118959"
variation 5392
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1035855570"
variation 5395..5398
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="tgct"
/replace="tgcttgct"
/db_xref="dbSNP:1420688359"
variation 5397
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1446906098"
variation 5399..5401
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="cc"
/replace="ccc"
/db_xref="dbSNP:2136900061"
variation 5400
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:139196876"
variation 5402
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:906035005"
variation 5404
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1593433642"
variation 5406
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:763183662"
variation 5409
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1950662556"
variation 5411
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="c"
/db_xref="dbSNP:1950662536"
variation 5411
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1472077154"
variation 5412
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:995270791"
variation 5413
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1593433630"
variation 5421
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950662367"
variation 5423
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:529242620"
variation 5424
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="a"
/db_xref="dbSNP:1346567997"
variation 5426
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1950662298"
variation 5428
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:893692737"
variation 5431
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950662258"
variation 5434
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1050122715"
variation 5436
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1728554875"
variation 5437..5450
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="aggcag"
/replace="aggcagagaggcag"
/db_xref="dbSNP:1282523584"
variation 5438
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1319629433"
variation 5440
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950662200"
variation 5441..5446
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="agag"
/replace="agagag"
/db_xref="dbSNP:1200768834"
variation 5441
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:578079820"
variation 5444
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1037132166"
variation 5446
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:943959114"
variation 5447
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950662112"
variation 5450
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950662077"
variation 5452
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:765603147"
variation 5453
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1950662034"
variation 5455
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950662021"
variation 5461
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:976518650"
variation 5462..5478
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="aggggcttccgccagca"
/replace="aggggcttccgccagcaggggcttccgccagca"
/db_xref="dbSNP:1950661873"
variation 5463..5466
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="gggg"
/replace="ggggg"
/db_xref="dbSNP:1950661977"
variation 5463
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:912506543"
variation 5464
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1950661990"
variation 5466
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:568369992"
variation 5467
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1309507815"
variation 5468
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2136899956"
variation 5469..5481
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="tccgccagcaagg"
/db_xref="dbSNP:1950661850"
variation 5469
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1315334057"
variation 5470..5487
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="ccgccagcaagggtttcc"
/db_xref="dbSNP:1202281967"
variation 5471
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:908293720"
variation 5472
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:546472066"
variation 5474
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:932453181"
variation 5475
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1463073978"
variation 5476
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="g"
/db_xref="dbSNP:1950661892"
variation 5477
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1950661888"
variation 5479
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1950661860"
variation 5480
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2136899921"
variation 5481
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1593433595"
variation 5482
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2543258133"
variation 5483..5486
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="tttc"
/db_xref="dbSNP:1950661825"
variation 5489
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1950661806"
variation 5490..5492
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="gtg"
/db_xref="dbSNP:2136899906"
variation 5490
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950661797"
variation 5491
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1593433593"
variation 5493
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:952869427"
variation 5495
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950661765"
variation 5497..5502
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="ccccc"
/replace="cccccc"
/replace="ccccccc"
/db_xref="dbSNP:1452683681"
variation 5497
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2136899900"
variation 5508
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:377292582"
variation 5509
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1471373002"
variation 5514
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950661706"
variation 5519
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1950661697"
variation 5521
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1328800656"
variation 5523
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1950661673"
variation 5524
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:2136899881"
variation 5527
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:925129882"
variation 5528
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1950661643"
variation 5530
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1470820372"
variation 5537
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950661621"
variation 5542
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:978790010"
variation 5544
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1443093072"
variation 5552
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1593433578"
variation 5559
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:969233323"
variation 5560
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950661511"
variation 5561
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:528308155"
variation 5562..5563
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="gg"
/db_xref="dbSNP:1227968074"
variation 5562
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:563934194"
variation 5567
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:989252509"
variation 5568
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1593433571"
variation 5569
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:960317376"
variation 5571
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1035907745"
variation 5573
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1278623006"
variation 5579
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1950661377"
variation 5580
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1021674632"
variation 5581
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1593433563"
variation 5582
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1010667774"
variation 5598
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1001797135"
variation 5599
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1234046977"
variation 5600
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1481887481"
variation 5601
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1643218747"
variation 5606
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:760288379"
variation 5607
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1950661269"
variation 5608
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:545555944"
variation 5610
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:76934175"
variation 5612
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:563211820"
variation 5614
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:932593241"
variation 5615
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1950661137"
variation 5618
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:1410395538"
variation 5621
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1172658741"
variation 5626
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1368728225"
variation 5628
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1409266414"
variation 5633
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1164776370"
variation 5635..5639
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="gaaag"
/replace="gaaagaaag"
/db_xref="dbSNP:1950661011"
variation 5636
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950661036"
variation 5639
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950660994"
variation 5640
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1347619857"
variation 5646
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1950660967"
variation 5648
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:541839411"
variation 5649
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1040691635"
variation 5657..5659
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="ttt"
/replace="ttttt"
/db_xref="dbSNP:1950660902"
variation 5665
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1340687070"
variation 5667
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1593433532"
variation 5669
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1566168391"
variation 5672
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:771890114"
variation 5673
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:939675599"
variation 5675
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1481065314"
variation 5676
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1950660772"
variation 5677
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:896929933"
variation 5679
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1015255046"
variation 5680
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1008267005"
variation 5681
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1211613020"
variation 5682
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1475711679"
variation 5683
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:574337015"
variation 5684
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1188264532"
variation 5686
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950660610"
variation 5694
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1220494818"
variation 5696
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950660584"
variation 5703
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1388219422"
variation 5704
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950660571"
variation 5706
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:931449372"
variation 5707
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:556137106"
variation 5708
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1950660508"
variation 5709..5714
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="ctgtcc"
/db_xref="dbSNP:1950660440"
variation 5709
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1950660493"
variation 5710
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:890805202"
variation 5711
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1246643548"
variation 5714..5730
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="cccgc"
/replace="cccgcggccgtgcccgc"
/db_xref="dbSNP:1950660181"
variation 5714
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:193187998"
variation 5716
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1352975620"
variation 5717
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950660389"
variation 5718
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1049603002"
variation 5719
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1327342389"
variation 5721..5722
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="cc"
/db_xref="dbSNP:1950660337"
variation 5722
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:960607826"
variation 5723
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1035951198"
variation 5726..5728
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="cc"
/replace="ccc"
/db_xref="dbSNP:1950660256"
variation 5726
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1225015339"
variation 5728
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:977360905"
variation 5729
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:967365814"
variation 5730
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:540924842"
variation 5731
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950660166"
variation 5736
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950660148"
variation 5737
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1950660128"
variation 5738..5743
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="ctccac"
/replace="ctccactccac"
/db_xref="dbSNP:1011644087"
variation 5741
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1950660107"
variation 5743
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:903676657"
variation 5744
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1288668424"
variation 5750
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1593433484"
variation 5752
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1210357243"
variation 5753
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:957887442"
variation 5755
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:2543257915"
variation 5756
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:573530194"
variation 5759
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1184292048"
variation 5760
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1028612118"
variation 5761
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:996693201"
variation 5762
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1950659872"
variation 5763
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="g"
/db_xref="dbSNP:1950659856"
variation 5766
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1043570169"
variation 5767
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:947487409"
variation 5768
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:2543257893"
variation 5770
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1318881471"
variation 5771
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:913345896"
variation 5772
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:901051123"
variation 5773
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:2543257887"
variation 5774
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1315161889"
variation 5775
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:988913975"
variation 5778
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950659699"
variation 5779
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1241951528"
variation 5781
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950659660"
variation 5783..5786
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="tctg"
/db_xref="dbSNP:1950659602"
variation 5783
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:1283309858"
variation 5784..5791
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="ctgagggc"
/db_xref="dbSNP:1204167948"
variation 5784
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950659621"
variation 5786
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:938649754"
variation 5787
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1210374145"
variation 5788..5790
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="ggg"
/db_xref="dbSNP:1950659546"
variation 5788
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1379047224"
variation 5789..5794
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="ggc"
/replace="ggcggc"
/db_xref="dbSNP:1950659459"
variation 5791
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:761534301"
variation 5792
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:544646696"
variation 5794
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1161351842"
variation 5796
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1364611833"
variation 5797
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2543257857"
variation 5801
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:774098477"
variation 5802
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:768603066"
variation 5803
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2136899568"
variation 5806
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950659369"
variation 5812
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1424678394"
variation 5813
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:980327990"
variation 5814
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1400690724"
variation 5815
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:916078353"
variation 5818
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1593433442"
variation 5819..5825
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="cttgcct"
/replace="cttgccttgcct"
/db_xref="dbSNP:1335989746"
variation 5824
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1332869849"
variation 5826
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1056328078"
variation 5828
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1286253268"
variation 5830
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1056216764"
variation 5833
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:970323842"
variation 5834
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:764238819"
variation 5835
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1223890435"
variation 5836
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1257747656"
variation 5840
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950658352"
variation 5842
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950658341"
variation 5843
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1223038459"
variation 5844
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:7316779"
variation 5849
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:974684952"
variation 5851
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2543257809"
variation 5855
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1258910683"
variation 5856
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:961567656"
variation 5859
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1950658265"
variation 5861
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:928855221"
variation 5862
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1950658215"
variation 5863
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:539610071"
variation 5865
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950658193"
variation 5866
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:144463331"
variation 5867
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:1481008482"
variation 5869
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:113364476"
variation 5873
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:2136899484"
variation 5874
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:890767500"
variation 5875
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1027968376"
variation 5876
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:914607113"
variation 5877
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:996707564"
variation 5878
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1411106718"
variation 5879
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1217100858"
variation 5880
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:535875372"
variation 5881
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1303051002"
variation 5886
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1251790736"
variation 5887
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:7296084"
variation 5888
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950657991"
variation 5891
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950657983"
variation 5894
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1950657972"
variation 5897
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1593433393"
variation 5898
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1667408182"
variation 5899
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1399837486"
variation 5903
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:945164832"
variation 5904
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:892309601"
variation 5907
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1593433380"
variation 5910
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:1950657822"
variation 5911
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:746029516"
variation 5912
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1193294629"
variation 5914
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:546533609"
variation 5915
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1194581364"
variation 5918
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1019523607"
variation 5919
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:72624274"
variation 5920
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1593433369"
variation 5921
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950657691"
variation 5922
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:886766909"
variation 5924
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1481540522"
variation 5925
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1458059995"
variation 5926
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1295089034"
variation 5931
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950657454"
variation 5934
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950657443"
variation 5935
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1365283625"
variation 5936
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:372491184"
variation 5938
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1593433358"
variation 5939
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950657395"
variation 5944
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:980130702"
variation 5946
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1950657361"
variation 5947
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1367256840"
variation 5948
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="t"
/replace="tt"
/db_xref="dbSNP:1593433349"
variation 5950
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:556871690"
variation 5954
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950657308"
variation 5955
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1430301510"
variation 5956..5961
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="ag"
/replace="agacag"
/db_xref="dbSNP:772039219"
variation 5957
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1296890596"
variation 5970
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950657261"
variation 5971
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1593433341"
variation 5977
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950657240"
variation 5978
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1223992352"
variation 5992
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:995186320"
variation 5995
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:948946629"
variation 5996
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:894183827"
variation 5999
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1188219387"
variation 6001
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950657142"
variation 6002
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:920133562"
variation 6003
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:1254896841"
variation 6007
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2543257657"
variation 6009
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1055563705"
variation 6014
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1423863125"
variation 6019..6032
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="gagtgctcaggacg"
/db_xref="dbSNP:1950656975"
variation 6019
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:974357908"
variation 6020
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1166517899"
variation 6021
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:961813972"
variation 6023
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:938826618"
variation 6024
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1950657044"
variation 6025
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1015781737"
variation 6026
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:551977987"
variation 6027
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1325219823"
variation 6028
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1390755458"
variation 6030
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:986936186"
variation 6031
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1296998563"
variation 6032
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:928833575"
variation 6034
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:747258534"
variation 6035
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1310935291"
variation 6036
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:955153208"
variation 6037
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1240211743"
variation 6038
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950656902"
variation 6041
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:7137283"
variation 6043..6051
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="tagtt"
/replace="tagttagtt"
/db_xref="dbSNP:1950656810"
variation 6045
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="g"
/db_xref="dbSNP:1208700967"
variation 6045
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:563433248"
variation 6047
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950656835"
variation 6049
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1950656821"
variation 6051
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:1244254674"
variation 6052
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:758800769"
variation 6053
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:369254436"
variation 6055
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1383259283"
variation 6056
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1366951777"
variation 6057
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1950656747"
variation 6058
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1593433273"
variation 6059..6066
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="cctg"
/replace="cctgcctg"
/db_xref="dbSNP:1950656691"
variation 6060
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950656729"
variation 6064
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1411203463"
variation 6065
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1422812989"
variation 6069
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="aa"
/db_xref="dbSNP:1159675781"
variation 6070
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1413844847"
variation 6071
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:541552507"
variation 6073
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:529742305"
variation 6074
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1593433261"
variation 6079
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1950656612"
variation 6080
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1022598323"
variation 6081
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1009502271"
variation 6084
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:892272922"
variation 6085
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1950656552"
variation 6086
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:976215773"
variation 6090
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:2136899215"
variation 6091
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:965572694"
variation 6093
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1593433251"
variation 6094
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1950656461"
variation 6095
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:559393410"
variation 6096
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950656433"
variation 6100
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:540986119"
variation 6104
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:2543257546"
variation 6108
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1950656399"
variation 6109
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950656383"
variation 6110
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950656362"
variation 6114
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:982694513"
variation 6115
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1056325184"
variation 6116
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:6560906"
variation 6120
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950656224"
variation 6123
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1026912623"
variation 6124
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:995553625"
variation 6132
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1950656158"
variation 6133
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:894162163"
variation 6136
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1593433234"
variation 6138
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1170239122"
variation 6140
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:2543257509"
variation 6141
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1464853467"
variation 6144
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1371115682"
variation 6145
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1182517554"
variation 6151
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1253488696"
variation 6154
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1950656013"
variation 6159
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950655996"
variation 6160
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1950655982"
variation 6161..6178
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="tg"
/replace="tgggccctgggaggagtg"
/db_xref="dbSNP:1158135207"
variation 6161
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1034497317"
variation 6162
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1950655914"
variation 6165
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950655882"
variation 6173
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950655864"
variation 6181
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:867681863"
variation 6184
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950655810"
variation 6185
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:558459821"
variation 6186
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1425803839"
variation 6188
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1950655764"
variation 6190
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950655748"
variation 6195
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1861651355"
variation 6197
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:907323623"
variation 6204
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950655699"
variation 6205
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1174071195"
variation 6210
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:2136899101"
variation 6211
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:1950655663"
variation 6212
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1950655647"
variation 6213
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1195145439"
variation 6215
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1002656712"
variation 6219
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:907376499"
variation 6221
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:774825335"
variation 6225
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950655567"
variation 6227
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:1044500135"
variation 6231
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1429017479"
variation 6233
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1041827427"
variation 6235
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2543257385"
variation 6241
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950655500"
variation 6242
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950655487"
variation 6249
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1409613286"
variation 6251
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950655444"
variation 6256
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950655429"
variation 6258
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:372816399"
variation 6262..6264
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="aaa"
/replace="aaaa"
/db_xref="dbSNP:1275745690"
variation 6262
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950655400"
variation 6264
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1255444936"
variation 6266
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:948663787"
variation 6269
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950655315"
variation 6270
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1217931534"
variation 6274
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1462293899"
variation 6277
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1566168204"
variation 6279
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:1311145652"
variation 6287
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:2543257355"
variation 6290
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1566168200"
variation 6291
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:2543257351"
variation 6292
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950655234"
variation 6293
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950655216"
variation 6298
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1205249562"
variation 6301
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950655171"
variation 6303
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="c"
/db_xref="dbSNP:1276408568"
variation 6308
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950655142"
variation 6312
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:919935542"
variation 6314
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1181223791"
variation 6318..6323
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="gtt"
/replace="gttgtt"
/db_xref="dbSNP:1247018207"
variation 6323
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:765838097"
variation 6324
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1039002820"
variation 6328
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1424362326"
variation 6329
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:546404177"
variation 6331
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:566500521"
variation 6333
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2543257322"
variation 6334
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:944813223"
variation 6337
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1228666774"
variation 6338
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1368950473"
variation 6339
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1950654772"
variation 6346
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1429306114"
variation 6349
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1324646929"
variation 6354
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950654721"
variation 6355
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:755408062"
variation 6357
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1434729790"
variation 6361
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1372096982"
variation 6365
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:2543257303"
variation 6367
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:987021454"
variation 6369
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2543257298"
variation 6371
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950654633"
variation 6377
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1228518442"
variation 6378
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950654598"
variation 6380
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:955124124"
variation 6381
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:2543257292"
variation 6383
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1593433162"
variation 6387
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1194920549"
variation 6389
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1454582694"
variation 6390
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950654513"
variation 6392
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1383628464"
variation 6394
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1290108510"
variation 6395
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:920974017"
variation 6396
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:866997220"
variation 6401
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1593433148"
variation 6402
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950654393"
variation 6404
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1246064885"
variation 6405
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1449928074"
variation 6406
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:373268048"
variation 6409
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1190631333"
variation 6410
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:1389884873"
variation 6414
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1448921102"
variation 6419
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950654287"
variation 6422..6425
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="aaaa"
/replace="aaaaa"
/db_xref="dbSNP:1164096387"
variation 6422
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2543257217"
variation 6424
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2543257216"
variation 6425
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1593433138"
variation 6427..6434
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="ctc"
/replace="ctcttctc"
/db_xref="dbSNP:1950654203"
variation 6427..6430
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="ct"
/replace="ctct"
/db_xref="dbSNP:1404011256"
variation 6429..6449
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="cttctcc"
/replace="cttctccctacctgcttctcc"
/db_xref="dbSNP:1950654108"
variation 6430
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1416225477"
variation 6431
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:1950654216"
variation 6434..6436
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="cc"
/replace="ccc"
/db_xref="dbSNP:1566168168"
variation 6434
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:2543257202"
variation 6435
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950654189"
variation 6436
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1950654153"
variation 6438
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1593433129"
variation 6443
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:967660618"
variation 6445
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2543257188"
variation 6446..6450
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="ct"
/replace="ctcct"
/db_xref="dbSNP:1950654076"
variation 6449
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1021982891"
variation 6452
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:2543257178"
variation 6453
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950654061"
variation 6454
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:2543257176"
variation 6457
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:2543257175"
variation 6458
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1398957307"
variation 6460
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1323241426"
variation 6461
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1026882257"
variation 6464
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1437839693"
variation 6465
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="g"
/db_xref="dbSNP:1950653991"
variation 6467
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950653975"
variation 6468..6469
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="cc"
/db_xref="dbSNP:1319102687"
variation 6470
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1169405435"
variation 6471
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1462327345"
variation 6473
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1950653907"
variation 6474
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950653892"
variation 6477
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1284480318"
variation 6479
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:2136898864"
variation 6481
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1226402752"
variation 6483
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:112455194"
variation 6484
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:575731514"
variation 6486..6487
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="ac"
/db_xref="dbSNP:2543257116"
variation 6486
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:750001086"
variation 6487
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1950653754"
variation 6488
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1566168151"
variation 6490
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:59220783"
variation 6492
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1446568344"
variation 6493
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1188318333"
variation 6497
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:112920524"
variation 6500..6506
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="aca"
/replace="acaaaca"
/db_xref="dbSNP:1002953910"
variation 6505..6528
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="cagcccctc"
/replace="cagcccctcaggtaccagcccctc"
/db_xref="dbSNP:1388525534"
variation 6505
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1177543346"
variation 6507
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2543257099"
variation 6509
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950653554"
variation 6511
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950653543"
variation 6513
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1003337204"
variation 6514
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:574541983"
variation 6516
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1950653485"
variation 6517
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1163075856"
variation 6518
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:552967878"
variation 6521
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2136898799"
variation 6523
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1252293357"
variation 6524
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2543257070"
variation 6525
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1459124151"
variation 6526
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1950653385"
variation 6527
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950653373"
variation 6528
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1044467182"
variation 6530
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2543257055"
variation 6534
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950653309"
variation 6535
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950653288"
variation 6537
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:534672285"
variation 6540
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2543257047"
variation 6541..6546
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="ctc"
/replace="ctcctc"
/db_xref="dbSNP:1445297908"
variation 6541
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1593433046"
variation 6543
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2543257041"
variation 6544
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2543257040"
variation 6546
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:570443541"
variation 6547
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1566168127"
variation 6550
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1593433035"
variation 6552
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1950653137"
variation 6557
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="t"
/replace="tt"
/db_xref="dbSNP:1292273179"
variation 6558
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:2543257020"
variation 6560
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:867840570"
variation 6562
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1566168123"
variation 6563
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1230001484"
variation 6564
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1055102024"
variation 6565
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:2136898745"
variation 6566
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:550312683"
variation 6567..6571
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="ccccc"
/replace="cccccc"
/db_xref="dbSNP:1201114261"
variation 6567
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950653011"
variation 6569
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1950652998"
variation 6571
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950652963"
variation 6572
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:914472800"
variation 6575
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1440748009"
variation 6576..6582
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="cgccagc"
/db_xref="dbSNP:2543256985"
variation 6576
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:552173468"
variation 6577
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:372705466"
variation 6578..6579
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="cc"
/replace="ccc"
/db_xref="dbSNP:1593433009"
variation 6578
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1950652840"
variation 6579
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950652808"
variation 6581
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950652790"
variation 6584
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:2543256981"
variation 6587
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1593433006"
variation 6589..6595
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="agtttcc"
/db_xref="dbSNP:1950652579"
variation 6589
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:900499228"
variation 6590
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:2543256978"
variation 6591..6593
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="tt"
/replace="ttt"
/db_xref="dbSNP:1950652610"
variation 6591
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:940258982"
variation 6592
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1180390627"
variation 6594..6599
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="ccccc"
/replace="cccccc"
/replace="ccccccc"
/db_xref="dbSNP:34214459"
variation 6594
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:908834441"
variation 6595
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1308585038"
variation 6598
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2543256962"
variation 6599
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:2543256950"
variation 6600
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:944697266"
variation 6602
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950652494"
variation 6604
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950652477"
variation 6605
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2543256936"
variation 6608
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1593432984"
variation 6609
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:907931110"
variation 6610
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1051289616"
variation 6611
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:2543256922"
variation 6612
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:2543256916"
variation 6613
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1411445777"
variation 6615
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:934126757"
variation 6616
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:983555885"
variation 6617
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1354053370"
variation 6618
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950652347"
variation 6620
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:929779066"
variation 6621
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1950652301"
variation 6623
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1343041569"
variation 6624..6627
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="aaca"
/replace="aacaaca"
/db_xref="dbSNP:2543256885"
variation 6625
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:1329830342"
variation 6629
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1210236376"
variation 6631
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2543256879"
variation 6634
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950652235"
variation 6637
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:769350561"
variation 6638
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:919800331"
variation 6641
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1180508636"
variation 6645
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="t"
/replace="tt"
/db_xref="dbSNP:1950652095"
variation 6646
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2543256868"
variation 6648
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:975110577"
variation 6649
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1950652058"
variation 6650..6654
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="ctc"
/replace="ctctc"
/db_xref="dbSNP:974391095"
variation 6650
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1434102587"
variation 6652
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:2543256856"
variation 6654
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:967797877"
variation 6655..6661
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="aaa"
/replace="aaaaaa"
/replace="aaaaaaa"
/replace="aaaaaaaa"
/db_xref="dbSNP:774495646"
variation 6656
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1452092288"
variation 6657
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:914879222"
variation 6659..6663
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="aaata"
/db_xref="dbSNP:2543256836"
variation 6659
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:958608805"
variation 6661
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950651924"
variation 6663
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="aa"
/db_xref="dbSNP:2543256834"
variation 6663
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2543256833"
variation 6664
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:2543256829"
variation 6665
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1157509011"
variation 6666
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950651890"
variation 6668
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:981042926"
variation 6670
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2543256819"
variation 6671
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2543256818"
variation 6674
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:987861676"
variation 6677
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:2543256816"
variation 6679
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2543256813"
variation 6680
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:2543256812"
variation 6681
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:2543256811"
variation 6683
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2543256809"
variation 6685
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1303390275"
variation 6686
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:956574912"
variation 6691..6697
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="tgtt"
/replace="tgttgtt"
/db_xref="dbSNP:1182092616"
variation 6691..6693
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="t"
/replace="tgt"
/db_xref="dbSNP:1365110869"
variation 6693..6698
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="tt"
/replace="ttgttt"
/db_xref="dbSNP:1950651739"
variation 6694
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:2543256799"
variation 6696..6702
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="ttt"
/replace="tttattt"
/db_xref="dbSNP:971054293"
variation 6696
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950651786"
variation 6697
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1233663783"
variation 6698
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:1298371889"
variation 6699
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1344608727"
variation 6700..6702
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="tt"
/replace="ttt"
/db_xref="dbSNP:2543256783"
variation 6701
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:2543256790"
variation 6703
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:2543256782"
variation 6706
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2543256777"
variation 6707
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:2136898542"
variation 6716
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1250941340"
variation 6718
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1489050547"
variation 6719
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1034908683"
variation 6725
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:537293461"
variation 6726
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2543256746"
variation 6730
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:2543256744"
variation 6731
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1267207842"
variation 6732
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:982035759"
variation 6733
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1381127530"
variation 6734
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1219245290"
variation 6735
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:969185223"
variation 6736
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2543256729"
variation 6739
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1192503955"
variation 6740
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950651492"
variation 6741
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1285558318"
variation 6742
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1023496417"
variation 6746
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950651430"
variation 6750
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1303919094"
variation 6753
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1291776862"
variation 6754
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1314191699"
variation 6758
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1167961222"
variation 6759
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2543256696"
variation 6762
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1372127454"
variation 6763
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1302006700"
variation 6766
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1218731854"
variation 6767
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1294998872"
variation 6768
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1366737523"
variation 6769
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1012992231"
variation 6770
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1401602595"
variation 6771
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950651238"
variation 6772..6788
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="ctgatgagc"
/replace="ctgatgagctgatgagc"
/replace="ctgatgagctgatgagctgatgagc"
/db_xref="dbSNP:1321113804"
variation 6772
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950651219"
variation 6775
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:898613434"
variation 6776
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1950651200"
variation 6780
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1297166812"
variation 6784
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950651168"
variation 6787
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:774958899"
variation 6788..6789
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="gt"
/db_xref="dbSNP:1950651084"
variation 6788
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1593432873"
variation 6789
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1017346754"
variation 6790
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:764871617"
variation 6792
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1176073398"
variation 6793
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1950651020"
variation 6794
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1432162608"
variation 6795
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950650984"
variation 6796
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="t"
/db_xref="dbSNP:1950650972"
variation 6796
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1423671354"
variation 6798
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:150580748"
variation 6799
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1468448609"
variation 6803
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1950650870"
variation 6806
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:1950650848"
variation 6807
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:2543256616"
variation 6809
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1478337536"
variation 6811
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1262864731"
variation 6812..6823
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="cccgcggcacaa"
/replace="cccgcggcacaacccgcggcacaa"
/db_xref="dbSNP:1256813220"
variation 6812
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950650798"
variation 6814
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1209959130"
variation 6815
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:996752517"
variation 6816
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:548318971"
variation 6817
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1484324450"
variation 6818
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950650718"
variation 6828
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1423989493"
variation 6829
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1209498593"
variation 6830
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1051259189"
variation 6831..6834
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="cccc"
/replace="ccccc"
/db_xref="dbSNP:2543256576"
variation 6832
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950650591"
variation 6833
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950650572"
variation 6834..6841
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="ct"
/replace="cttcctct"
/db_xref="dbSNP:760536621"
variation 6834..6835
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="gacagagg"
/db_xref="dbSNP:763608657"
variation 6834
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1261153364"
variation 6835
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1460698375"
variation 6837
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2136898346"
variation 6838
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1220437346"
variation 6839
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1341076723"
variation 6840
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2543256562"
variation 6841
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1041040639"
variation 6842
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1593432838"
variation 6844
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:190044764"
variation 6845
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:746915737"
variation 6848
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950649725"
variation 6852
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2543256549"
variation 6853
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1465091341"
variation 6855
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1356974856"
variation 6857..6879
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="cggttgtctccttctgaggcggt"
/replace="cggttgtctccttctgaggcggttgtctccttctgaggcggt"
/db_xref="dbSNP:1240059249"
variation 6857
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:185169650"
variation 6858
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:771703202"
variation 6859
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950649624"
variation 6862
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1423552758"
variation 6864
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2543256530"
variation 6866
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1950649595"
variation 6867..6871
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="ct"
/replace="cttct"
/db_xref="dbSNP:930750903"
variation 6867
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1047833323"
variation 6870
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1168893990"
variation 6875
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1270588134"
variation 6876
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1257106656"
variation 6877
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1181547576"
variation 6878
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:899995140"
variation 6881
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2136898276"
variation 6882
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1199366115"
variation 6885..6889
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="t"
/replace="tagat"
/db_xref="dbSNP:1259580201"
variation 6885
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1213067482"
variation 6887
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1318428533"
variation 6888
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1950649376"
variation 6889
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1950649333"
variation 6890
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950649305"
variation 6891
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1257421140"
variation 6892
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:547437304"
variation 6893..6896
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="gggg"
/replace="ggggg"
/db_xref="dbSNP:775496587"
variation 6895
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2136898254"
variation 6896
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2543256467"
variation 6897
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1483277534"
variation 6898
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1323331886"
variation 6901..6903
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="aaa"
/replace="aaaa"
/db_xref="dbSNP:1312944792"
variation 6901
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1198996239"
variation 6904
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:920676391"
variation 6908
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:2543256457"
variation 6909
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950649159"
variation 6910..6915
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="caca"
/replace="cacaca"
/db_xref="dbSNP:2543256446"
variation 6910
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950649137"
variation 6912
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1395046847"
variation 6913
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1414097796"
variation 6914
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1380159160"
variation 6915
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1398842803"
variation 6916
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1158508463"
variation 6917
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1332730093"
variation 6919..6924
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="ca"
/replace="cagaca"
/db_xref="dbSNP:1359870309"
variation 6919
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1566167983"
variation 6921
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1663611044"
variation 6922
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1446893597"
variation 6923
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1400210605"
variation 6925
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1467623041"
variation 6927
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2543256424"
variation 6928
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1950648934"
variation 6929
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950648916"
variation 6931
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1039880040"
variation 6932
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:946453272"
variation 6933
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1410829597"
variation 6935
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:143642745"
variation 6936
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1371838616"
variation 6938
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950648785"
variation 6940
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1593432769"
variation 6945
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:568978548"
variation 6946..6947
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="ctc"
/db_xref="dbSNP:2543256400"
variation 6948
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:988302054"
variation 6949
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:2543256394"
variation 6951
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1279914381"
variation 6953
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2136898172"
variation 6956
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="c"
/db_xref="dbSNP:2543256390"
variation 6958
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:2543256389"
variation 6959..6965
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="ag"
/replace="aggagag"
/db_xref="dbSNP:1950648701"
variation 6959
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950648720"
variation 6965
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1263016928"
variation 6968
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1191683719"
variation 6970
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:747759933"
variation 6974
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2543256368"
variation 6976
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1950648622"
variation 6981
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950648608"
variation 6983
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:2543256364"
variation 6984
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1825338461"
variation 6986
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1950648591"
variation 6987
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2543256357"
variation 6991
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950648573"
variation 6992..7171
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="gtgagtgccgtgcgccgtgctgggagcctgtcactgtgag"
/replace="gtgagtgccgtgcgccgtgctgggagcctgtcactgtgagtgccgtgc
gccgtgctgggagcctgtcactgtgagtgccgtgcgccgtgctgggagcctgtcactg
tgagtgccgtgcgccctgctgggagcctgtcactgtgagtgccgtgcgccgtgctggg
agcctgtcactgtgag"
/db_xref="dbSNP:1950646864"
variation 6992..7112
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="gtgagtgccgtgcgcc"
/replace="gtgagtgccgtgcgccgtgctgggagcctgtcactgtgagtgccgtgc
gcc"
/replace="gtgagtgccgtgcgccgtgctgggagcctgtcactgtgagtgccgtgc
gccgtgctgggagcctgtcactgtgagtgccgtgcgcc"
/replace="gtgagtgccgtgcgccgtgctgggagcctgtcactgtgagtgccgtgc
gccgtgctgggagcctgtcactgtgagtgccgtgcgccgtgctgggagcctgtcactg
tgagtgccgtgcgcc"
/db_xref="dbSNP:1593432686"
variation 6992
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="gcctggcactg"
/db_xref="dbSNP:2543256353"
variation 6993
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:927636444"
variation 6994..7027
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="gagtgccgtgcgccgtgctgggagcctgtcactg"
/replace="gagtgccgtgcgccgtgctgggagcctgtcactgggagtgccgtgcgc
cgtgctgggagcctgtcactg"
/db_xref="dbSNP:1950648398"
variation 6998..7276
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="gccgtgcgccgtgctgggagcctgtcactgtgag"
/replace="gccgtgcgccgtgctgggagcctgtcactgtgagtgccgtgcgccgtg
ctgggagcctgtcactgtgagtgccgtgcgccgtgctgggagcctgtcactgtgagtg
ccgtgcgccctgctgggagcctgtcactgtgagtgccgtgcgccgtgctgggagcctg
tcactgtgagggccgagcgccgtgctgggagcctgtcactgtgagggccgtgcgccgt
gctgggagcctgtcactgtgagggccgtgcgccgtgctgggagcctgtcactgtgag"
/db_xref="dbSNP:1950645810"
variation 7000
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1285040645"
variation 7001
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950648519"
variation 7002
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:2543256346"
variation 7003..7206
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="gcgccgtgctgggagcctgtcactgtgag"
/replace="gcgccgtgctgggagcctgtcactgtgagtgccgtgcgccgtgctggg
agcctgtcactgtgagtgccgtgcgccgtgctgggagcctgtcactgtgagtgccgtg
cgccctgctgggagcctgtcactgtgagtgccgtgcgccgtgctgggagcctgtcact
gtgagggccgagcgccgtgctgggagcctgtcactgtgag"
/db_xref="dbSNP:1950646461"
variation 7003..7036
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="gcgccgtgctgggagcctgtcactgtgagtgccg"
/db_xref="dbSNP:2543256312"
variation 7003..7031
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="gcgccgtgctgggagcctgtcactgtgag"
/replace="gcgccgtgctgggagcctgtcactgtgagggccgagcgccgtgctggg
agcctgtcactgtgag"
/db_xref="dbSNP:1950648358"
variation 7003..7006
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="gcgc"
/replace="gcgctgtgctgggagcctgtcactgtgagggccgagcgc"
/db_xref="dbSNP:2543256341"
variation 7004
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1199987350"
variation 7005..7038
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="gccgtgctgggagcctgtcactgtgagtgccgtg"
/replace="gccgtgctgggagcctgtcactgtgagtgccgtgagccgtgctgggag
cctgtcactgtgagtgccgtg"
/replace="gccgtgctgggagcctgtcactgtgagtgccgtgtgccgtgctgggag
cctgtcactgtgagtgccgtg"
/db_xref="dbSNP:1950648286"
variation 7005
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950648496"
variation 7007
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:982006238"
variation 7008
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1321649348"
variation 7018
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1176594058"
variation 7019
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2543256336"
variation 7021
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:564803571"
variation 7022..7055
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="tcactgtgagtgccgtgcgccgtgctgggagcct"
/db_xref="dbSNP:2136898029"
variation 7022
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1023465397"
variation 7026..7064
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="tg"
/replace="tgtgagtgccgtgcgccgtgctgggagcctgtcactgtg"
/db_xref="dbSNP:2543256270"
variation 7026..7029
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="tg"
/replace="tgtg"
/db_xref="dbSNP:1950648369"
variation 7026
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1345924298"
variation 7028
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:973271315"
variation 7031
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2136898094"
variation 7032..7135
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="tgccgtgcgccgtgctgggagcctgtcactgtgagtgccgtgcgccgt
gctgggagcctgtcactgtgagtgccgtgcgccctgctgggagcctgtcactgtga"
/db_xref="dbSNP:1566167877"
variation 7032
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:112963065"
variation 7033..7046
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="gccgtgcgccgtgc"
/replace="gccgtgcgccgtgcgccgtgc"
/db_xref="dbSNP:1178149453"
variation 7035
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1328168684"
variation 7036
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950648311"
variation 7037
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:112315828"
variation 7038..7206
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="gcgccgtgctgggagcctgtcactgtgag"
/replace="gcgccgtgctgggagcctgtcactgtgagtgccgtgcgccgtgctggg
agcctgtcactgtgagtgccgtgcgccctgctgggagcctgtcactgtgagtgccgtg
cgccgtgctgggagcctgtcactgtgagggccgagcgccgtgctgggagcctgtcact
gtgag"
/db_xref="dbSNP:1950646445"
variation 7038..7106
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="gcgccgtgctgggagcctgtcactgtgagtgccgtgcgccgtgctggg
agcctgtcactgtgagtgccg"
/replace="gcgccgtgctgggagcctgtcactgtgagtgccgtgcgccgtgctggg
agcctgtcactgtgagtgccgagcgccgtgctgggagcctgtcactgtgagtgccgtg
cgccgtgctgggagcctgtcactgtgagtgccg"
/db_xref="dbSNP:1950647495"
variation 7038..7071
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="gcgccgtgctgggagcctgtcactgtgagtgccg"
/replace="gcgccgtgctgggagcctgtcactgtgagtgccgagcgccgtgctggg
agcctgtcactgtgagtgccg"
/db_xref="dbSNP:2543256254"
variation 7038..7066
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="gcgccgtgctgggagcctgtcactgtgag"
/replace="gcgccgtgctgggagcctgtcactgtgagggccgagcgccgtgctggg
agcctgtcactgtgag"
/db_xref="dbSNP:1950648073"
variation 7038..7041
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="gc"
/replace="gcgc"
/db_xref="dbSNP:2543256297"
variation 7039
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:372406095"
variation 7040
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950648249"
variation 7041
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1950648232"
variation 7042..7106
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="cgtgctgggagcctgtcactgtgagtgccgtgcgccgtgctgggagcc
tgtcactgtgagtgccg"
/db_xref="dbSNP:2543256201"
variation 7042
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1016985244"
variation 7043
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1403391406"
variation 7046
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950648182"
variation 7052
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2543256281"
variation 7053
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950648159"
variation 7054
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950648152"
variation 7056
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1950648133"
variation 7057
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="t"
/db_xref="dbSNP:2136898022"
variation 7057
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:867949638"
variation 7061..7064
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="tg"
/replace="tgtg"
/db_xref="dbSNP:1950648092"
variation 7062
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1593432721"
variation 7065
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:1950648083"
variation 7066..7074
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="gtgc"
/replace="gtgccgtgc"
/db_xref="dbSNP:1950647931"
variation 7066..7073
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="gtgccgtg"
/replace="gtgccgtgtgccgtg"
/db_xref="dbSNP:1203482269"
variation 7067..7100
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="tgccgtgcgccgtgctgggagcctgtcactgtga"
/db_xref="dbSNP:1950647603"
variation 7067
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:369912494"
variation 7069
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950648043"
variation 7070
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1950648033"
variation 7071
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1276299904"
variation 7072
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:112253969"
variation 7073..7076
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="gc"
/replace="gcgc"
/db_xref="dbSNP:2543256234"
variation 7073
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1950647951"
variation 7074..7078
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="cgccg"
/replace="cgccgccg"
/db_xref="dbSNP:1950647863"
variation 7074
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1247217948"
variation 7075
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950647896"
variation 7077
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1166586922"
variation 7078
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="g"
/db_xref="dbSNP:1243253802"
variation 7078
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:867813773"
variation 7079..7147
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="tgctgggagcctgtcactgtgagtgccgtgcgcc"
/replace="tgctgggagcctgtcactgtgagtgccgtgcgccctgctgggagcctg
tcactgtgagtgccgtgcgcc"
/replace="tgctgggagcctgtcactgtgagtgccgtgcgccctgctgggagcctg
tcactgtgagtgccgtgcgccctgctgggagcctgtcactgtgagtgccgtgcgcc"
/replace="tgctgggagcctgtcactgtgagtgccgtgcgccctgctgggagcctg
tcactgtgagtgccgtgcgccctgctgggagcctgtcactgtgagtgccgtgcgccct
gctgggagcctgtcactgtgagtgccgtgcgcc"
/db_xref="dbSNP:1566167860"
variation 7080
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1394605523"
variation 7082
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950647795"
variation 7084
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950647772"
variation 7088
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:981347138"
variation 7090
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950647730"
variation 7092
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1186874778"
variation 7094
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1950647700"
variation 7095..7096
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="ct"
/db_xref="dbSNP:1324546343"
variation 7095
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1950647687"
variation 7096..7099
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="tg"
/replace="tgtg"
/db_xref="dbSNP:1325803117"
variation 7096
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1409766089"
variation 7097
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1439282385"
variation 7101..7113
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="gtgccgtgcgccc"
/db_xref="dbSNP:1950647324"
variation 7102
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="t"
/db_xref="dbSNP:1950647586"
variation 7102
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:12810980"
variation 7104
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950647537"
variation 7105
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1228493149"
variation 7106
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:546169012"
variation 7107
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:12810974"
variation 7108
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950647412"
variation 7109..7113
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="cgccc"
/db_xref="dbSNP:2543256185"
variation 7109
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:971023272"
variation 7110
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1290260414"
variation 7113
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:12830326"
variation 7114..7241
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="tgctgggagcctgtcactgtgag"
/replace="tgctgggagcctgtcactgtgagtgccgtgcgccgtgctgggagcctg
tcactgtgagggccgagcgccgtgctgggagcctgtcactgtgagggccgtgcgccgt
gctgggagcctgtcactgtgag"
/db_xref="dbSNP:1950646119"
variation 7114..7206
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="tgctgggagcctgtcactgtgag"
/replace="tgctgggagcctgtcactgtgagtgccgtgcgccgtgctgggagcctg
tcactgtgagggccgagcgccgtgctgggagcctgtcactgtgag"
/db_xref="dbSNP:1950646430"
variation 7114..7171
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="tgctgggagcctgtcactgtgag"
/replace="tgctgggagcctgtcactgtgagtgccgtgcgccgtgctgggagcctg
tcactgtgag"
/db_xref="dbSNP:1950646814"
variation 7115
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1245131236"
variation 7127..7160
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="tcactgtgagtgccgtgcgccgtgctgggagcct"
/db_xref="dbSNP:2136897777"
variation 7127
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1211783477"
variation 7128
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1017900401"
variation 7129
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2543256176"
variation 7130
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1950647238"
variation 7131
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1252292908"
variation 7132
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1190526003"
variation 7137
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="t"
/db_xref="dbSNP:1317587449"
variation 7137
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:11147105"
variation 7138..7246
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="gccgtgcgccgtgctgggagcctgtcactgtgagggccg"
/replace="gccgtgcgccgtgctgggagcctgtcactgtgagggccgagcgccgtg
ctgggagcctgtcactgtgagggccgtgcgccgtgctgggagcctgtcactgtgaggg
ccg"
/db_xref="dbSNP:1950646062"
variation 7138..7176
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="gccgtgcgccgtgctgggagcctgtcactgtgagggccg"
/replace="gccgtgcgccgtgctgggagcctgtcactgtgagggccgtgcgccgtg
ctgggagcctgtcactgtgagggccg"
/db_xref="dbSNP:2543256120"
variation 7138..7151
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="gccgtgcgccgtgc"
/replace="gccgtgcgccgtgcgccgtgc"
/db_xref="dbSNP:1319669476"
variation 7138..7147
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="gccgtgcgcc"
/replace="gccgtgcgccctgctgggagcctgtcactgtgagggccgtgcgcc"
/db_xref="dbSNP:2543256155"
variation 7140
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:575839323"
variation 7141
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950647113"
variation 7142
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:113380611"
variation 7143..7211
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="gcgccgtgctgggagcctgtcactgtgagggccg"
/replace="gcgccgtgctgggagcctgtcactgtgagggccgagcgccgtgctggg
agcctgtcactgtgagggccg"
/replace="gcgccgtgctgggagcctgtcactgtgagggccgagcgccgtgctggg
agcctgtcactgtgagggccgagcgccgtgctgggagcctgtcactgtgagggccg"
/db_xref="dbSNP:1566167814"
variation 7144
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1416476537"
variation 7145
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1460177768"
variation 7147..7181
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="cgtgctgggagcctgtcactgtgagggccgagcgc"
/db_xref="dbSNP:2543256102"
variation 7147..7148
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="ctgtgagtgccgtgcgccctgctgggagcctgtca"
/db_xref="dbSNP:1422324288"
variation 7147
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="cctgctgggagcctgtcactgtgagtgccgtgc"
/db_xref="dbSNP:1950647026"
variation 7147
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1271980235"
variation 7148..7149
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="ccc"
/db_xref="dbSNP:1950646949"
variation 7148
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:373750424"
variation 7152
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:2543256144"
variation 7153..7154
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="acca"
/db_xref="dbSNP:2543256142"
variation 7162
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="t"
/db_xref="dbSNP:2136897772"
variation 7162
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1324340182"
variation 7164
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1950646894"
variation 7166
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1429646634"
variation 7169..7180
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="gagggccgagcg"
/db_xref="dbSNP:2543256106"
variation 7171..7202
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="gggccgagcgccgtgctgggagcctgtcactg"
/db_xref="dbSNP:1950646509"
variation 7172
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:12825070"
variation 7175
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1357207042"
variation 7176
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1231210218"
variation 7177
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:12816572"
variation 7179
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:567731158"
variation 7180
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1446479095"
variation 7182
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:563731168"
variation 7183
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="g"
/db_xref="dbSNP:2136897708"
variation 7183
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:12825062"
variation 7197
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1187613529"
variation 7198..7231
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="cactgtgagggccgtgcgccgtgctgggagcctg"
/replace="cactgtgagggccgtgcgccgtgctgggagcctggcactgtgagggcc
gtgcgccgtgctgggagcctg"
/db_xref="dbSNP:2136897622"
variation 7198
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1413381071"
variation 7199
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1593432633"
variation 7200
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1950646538"
variation 7201..7204
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="tg"
/replace="tgtg"
/db_xref="dbSNP:1950646488"
variation 7201
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950646524"
variation 7204..7208
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="gaggg"
/db_xref="dbSNP:1950646375"
variation 7207
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:34264324"
variation 7210
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1270728071"
variation 7211..7215
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="gtgcg"
/replace="gtgcggtgcg"
/db_xref="dbSNP:1950646244"
variation 7211
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1950646304"
variation 7212
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:866923683"
variation 7213
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950646273"
variation 7214
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1334467658"
variation 7215
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1831225152"
variation 7216
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1950646230"
variation 7217
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2543256043"
variation 7218
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:12825028"
variation 7223
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:56333035"
variation 7231
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950646165"
variation 7232
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1593432615"
variation 7242
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:12825010"
variation 7246
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1566167803"
variation 7247
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:374276918"
variation 7249
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950645997"
variation 7251
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1351057073"
variation 7252
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1241158811"
variation 7253
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1350136939"
variation 7255
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950645880"
variation 7259
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:2543255998"
variation 7265
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950645863"
variation 7266
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950645846"
variation 7267
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:374352587"
variation 7268..7311
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="cactgtgagggccgtgcgccgtgctgggagcctggcactgtgag"
/replace="cactgtgagggccgtgcgccgtgctgggagcctggcactgtgagggcc
gtgcgccgtgctgggagcctggcactgtgag"
/db_xref="dbSNP:2136897528"
variation 7277
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:111955070"
variation 7278..7586
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="gccgtgcgccgtgctgggagcctggcactgtgagtgccgtgcgccgtg
ctgggagcctggcact"
/replace="gccgtgcgccgtgctgggagcctggcactgtgagtgccgtgcgccgtg
ctgggagcctggcactgtgagggccgtgcgccgtgctgggagcctggcactgtgagtg
ccgtgcgccgtgctgggagcctgtcactgtgagtgccgtgcgccgtgctgggagcctg
tcactgtgagtgccgtgcgccgtgctgggagcctggcactgtgagtgccgtgcgccgt
gctgggagcctggcactgtgagtgccgtgcgccgtgctgggagcctggcactgtgagt
gccgtgcgccgtgctgggagcctggcact"
/db_xref="dbSNP:1950643683"
variation 7278..7441
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="gccgtgcgccgtgctgggagcctg"
/replace="gccgtgcgccgtgctgggagcctggcactgtgagtgccgtgcgccgtg
ctgggagcctggcactgtgagggccgtgcgccgtgctgggagcctggcactgtgagtg
ccgtgcgccgtgctgggagcctgtcactgtgagtgccgtgcgccgtgctgggagcctg
"
/db_xref="dbSNP:2543255818"
variation 7278..7346
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="gccgtgcgccgtgctgggagcctggcactgtgag"
/replace="gccgtgcgccgtgctgggagcctggcactgtgagtgccgtgcgccgtg
ctgggagcctggcactgtgag"
/replace="gccgtgcgccgtgctgggagcctggcactgtgagtgccgtgcgccgtg
ctgggagcctggcactgtgagtgccgtgcgccgtgctgggagcctggcactgtgag"
/db_xref="dbSNP:1566167782"
variation 7278..7291
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="gccgtgc"
/replace="gccgtgcgccgtgc"
/db_xref="dbSNP:1950645651"
variation 7280
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950645791"
variation 7281
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1593432595"
variation 7282
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:34321921"
variation 7284
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950645733"
variation 7285
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950645713"
variation 7287
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1210640554"
variation 7288
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:112416184"
variation 7293
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:112952300"
variation 7300
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950645622"
variation 7302
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:370851235"
variation 7303..7311
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="cactgtgag"
/replace="cactgtgagggccgtgcgccgtgctgggagcctgtcactgtgag"
/db_xref="dbSNP:2136897522"
variation 7307
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1338202795"
variation 7308
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950645553"
variation 7312
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="t"
/db_xref="dbSNP:1353603352"
variation 7312
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:11147104"
variation 7313..7381
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="gccgtgcgccgtgctgggagcctggcactgtgag"
/replace="gccgtgcgccgtgctgggagcctggcactgtgagggccgtgcgccgtg
ctgggagcctggcactgtgag"
/db_xref="dbSNP:1566167771"
variation 7316
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1469192389"
variation 7319
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950645479"
variation 7320
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2543255938"
variation 7322
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1172582585"
variation 7323
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1950645445"
variation 7328
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1593432579"
variation 7333
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1593432578"
variation 7334
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1593432573"
variation 7335
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950645383"
variation 7336
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1593432570"
variation 7337..7369
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="gcactgtgagggccgtgcgccgtgctgggagcc"
/db_xref="dbSNP:2543255892"
variation 7337
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:33939349"
variation 7342..7374
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="gtgagggccgtgcgccgtgctgggagcctggca"
/db_xref="dbSNP:1443386902"
variation 7342
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:879564616"
variation 7346..7347
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="tgccgtgcgccgtgctgggagcctggcactgtga"
/db_xref="dbSNP:2136897464"
variation 7347
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:74473743"
variation 7348..7586
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="gccgtgcgccgtgctgggagcctggcactgtgagtgccgtgcgccgtg
ctgggagcctgtcactgtgagtgccgtgcgccgtgctgggagcctgtcactgtgagtg
ccgtgcgccgtgctgggagcctggcactgtgagtgccgtgcgccgtgctgggagcctg
gcactgtgagtgccgtgcgccgtgctgggagcctggcactgtgagtgccgtgcgccgt
gctgggagcctggcact"
/replace="gccgtgcgccgtgctgggagcctggcactgtgagtgccgtgcgccgtg
ctgggagcctgtcactgtgagtgccgtgcgccgtgctgggagcctgtcactgtgagtg
ccgtgcgccgtgctgggagcctggcactgtgagtgccgtgcgccgtgctgggagcctg
gcactgtgagtgccgtgcgccgtgctgggagcctggcactgtgagtgccgtgcgccgt
gctgggagcctggcactgtgagtgccgtgcgccgtgctgggagcctgtcactgtgagt
gccgtgcgccgtgctgggagcctgtcactgtgagtgccgtgcgccgtgctgggagcct
ggcactgtgagtgccgtgcgccgtgctgggagcctggcactgtgagtgccgtgcgccg
tgctgggagcctggcactgtgagtgccgtgcgccgtgctgggagcctggcact"
/db_xref="dbSNP:71076481"
variation 7348..7511
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="gccgtgcgccgtgctgggagcctggcactgtgagtgccgtgcgccgtg
ctgggagcctg"
/replace="gccgtgcgccgtgctgggagcctggcactgtgagtgccgtgcgccgtg
ctgggagcctgtcactgtgagtgccgtgcgccgtgctgggagcctgtcactgtgagtg
ccgtgcgccgtgctgggagcctggcactgtgagtgccgtgcgccgtgctgggagcctg
"
/db_xref="dbSNP:1950644157"
variation 7348..7406
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="gccgtgcgccgtgctgggagcctg"
/replace="gccgtgcgccgtgctgggagcctggcactgtgagtgccgtgcgccgtg
ctgggagcctg"
/replace="gccgtgcgccgtgctgggagcctggcactgtgagtgccgtgcgccgtg
ctgggagcctggcactgtgagtgccgtgcgccgtgctgggagcctg"
/db_xref="dbSNP:2136897395"
variation 7349
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1593432563"
variation 7351
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1593432559"
variation 7352
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:1420800695"
variation 7354
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950645165"
variation 7355
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950645143"
variation 7357
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1392918844"
variation 7367
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1326843871"
variation 7370
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950645087"
variation 7371..7547
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="ggcactgtgagtgccgtgcgccgtgctgggagcctgtcactgtgagtg
ccgtgcgccgtgctgggagcctgtcactgtgagtgccgtgcgccgtgctgggagcctg
gcactgtgagtgccgtgcgccgtgctgggagcctggcactgtgagtgccgtgcgccgt
gctgggagcctgg"
/db_xref="dbSNP:1555267717"
variation 7371..7372
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="gg"
/db_xref="dbSNP:2543255887"
variation 7372
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:113443340"
variation 7373..7476
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="cactgtgagtgccgtgcgccgtgctgggagcctgtcactgtgagtgcc
gtgcgccgtgctgggagcctg"
/replace="cactgtgagtgccgtgcgccgtgctgggagcctgtcactgtgagtgcc
gtgcgccgtgctgggagcctgtcactgtgagtgccgtgcgccgtgctgggagcctg"
/replace="cactgtgagtgccgtgcgccgtgctgggagcctgtcactgtgagtgcc
gtgcgccgtgctgggagcctgtcactgtgagtgccgtgcgccgtgctgggagcctgtc
actgtgagtgccgtgcgccgtgctgggagcctg"
/db_xref="dbSNP:1950644373"
variation 7374
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1950645027"
variation 7376..7379
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="tg"
/replace="tgtg"
/db_xref="dbSNP:1184328686"
variation 7377
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:372645881"
variation 7382
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:369325349"
variation 7385
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2543255861"
variation 7386
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950644944"
variation 7387
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:1950644933"
variation 7389
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950644920"
variation 7392
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950644907"
variation 7393
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1593432538"
variation 7401
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:1480417143"
variation 7405
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950644716"
variation 7406..7547
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="gtcactgtgagtgccgtgcgccgtgctgggagcctgtcactgtgagtg
ccgtgcgccgtgctgggagcctggcactgtgagtgccgtgcgccgtgctgggagcctg
gcactgtgagtgccgtgcgccgtgctgggagcctgg"
/db_xref="dbSNP:869091822"
variation 7406
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1950644700"
variation 7407
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:377606697"
variation 7412
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1950644657"
variation 7413..7651
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="tgagtgccgtgcgccgtgctgggagcctgtcactgtgagtgccgtgcg
ccgtgctgggagcctg"
/replace="tgagtgccgtgcgccgtgctgggagcctgtcactgtgagtgccgtgcg
ccgtgctgggagcctggcactgtgagtgccgtgcgccgtgctgggagcctggcactgt
gagtgccgtgcgccgtgctgggagcctggcactgtgagtgccgtgcgccgtgctggga
gcctggcactctgagtgccgtgcgccgtgctgggagcctgtcactgtgagtgccgtgc
gccgtgctgggagcctg"
/db_xref="dbSNP:1566167708"
variation 7417
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:374127317"
variation 7420
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1950644609"
variation 7424
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1593432522"
variation 7425
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950644575"
variation 7427
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1233893012"
variation 7428
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:369702042"
variation 7429..7462
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="tgctgggagcctgtcactgtgagtgccgtgcgcc"
/replace="tgctgggagcctgtcactgtgagtgccgtgcgccatgctgggagcctg
tcactgtgagtgccgtgcgcc"
/db_xref="dbSNP:2543255797"
variation 7441
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950644530"
variation 7442
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:567317801"
variation 7443..7586
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="cactgtgagtgccgtgcgccgtgctgggagcctggcact"
/replace="cactgtgagtgccgtgcgccgtgctgggagcctggcactgtgagtgcc
gtgcgccgtgctgggagcctggcact"
/replace="cactgtgagtgccgtgcgccgtgctgggagcctggcactgtgagtgcc
gtgcgccgtgctgggagcctggcactgtgagtgccgtgcgccgtgctgggagcctggc
actgtgagtgccgtgcgccgtgctgggagcctggcact"
/db_xref="dbSNP:1950643657"
variation 7448..7616
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="tgagtgccgtgcgccgtgctgggagcctg"
/replace="tgagtgccgtgcgccgtgctgggagcctggcactgtgagtgccgtgcg
ccgtgctgggagcctggcactgtgagtgccgtgcgccgtgctgggagcctggcactgt
gagtgccgtgcgccgtgctgggagcctggcactctgagtgccgtgcgccgtgctggga
gcctg"
/db_xref="dbSNP:2543255612"
variation 7452
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:867118660"
variation 7460
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1950644459"
variation 7461
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1950644445"
variation 7462
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1273559686"
variation 7463
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1593432511"
variation 7477..7544
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="gcactgtgagtgccgtgcgccgtgctgggagcctggcactgtgagtgc
cgtgcgccgtgctgggagcc"
/db_xref="dbSNP:2543255702"
variation 7477..7509
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="gcactgtgagtgccgtgcgccgtgctgggagcc"
/db_xref="dbSNP:1950644168"
variation 7477..7486
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="gcactgtgag"
/db_xref="dbSNP:1950644298"
variation 7477
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:34241647"
variation 7478..7720
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="cactgtgagtgccgtgcgccgtgctgggagcctggcactgtgagtgcc
gtgcgccgtgctgggagcct"
/replace="cactgtgagtgccgtgcgccgtgctgggagcctggcactgtgagtgcc
gtgcgccgtgctgggagcctggcactgtgagtgccgtgcgccgtgctgggagcctggc
actctgagtgccgtgcgccgtgctgggagcctgtcactgtgagtgccgtgcgccgtgc
tgggagcctgtcactgtgagtgccgtgcgccgtgctgggagcctggcactgtgagtgc
cgtgcgccgtgctgggagcct"
/db_xref="dbSNP:1950642502"
variation 7478..7651
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="cactgtgagtgccgtgcgccgtgctgggagcctg"
/replace="cactgtgagtgccgtgcgccgtgctgggagcctggcactgtgagtgcc
gtgcgccgtgctgggagcctggcactgtgagtgccgtgcgccgtgctgggagcctggc
actctgagtgccgtgcgccgtgctgggagcctgtcactgtgagtgccgtgcgccgtgc
tgggagcctg"
/db_xref="dbSNP:1566167707"
variation 7482
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:36046850"
variation 7487
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:111428481"
variation 7491
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1245135958"
variation 7492
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:879109892"
variation 7494
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950644235"
variation 7497..7701
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="cgtgctgggagcctggcactgtgagtgccgtgcgccgtgctgggagcc
tggcactgtgagtgccgtgcgccgtgctgggagcctggcactctgagtgccgtgcgcc
gtgctgggagcctgtcactgtgagtgccgtgcgccgtgctgggagcctgtcactgtga
gtgccgtgcgccgtgctgggagcctggcactgtgagtgccg"
/db_xref="dbSNP:1566167675"
variation 7497
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1172703426"
variation 7498..7766
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="gtgctgggagcctggcactgtgag"
/replace="gtgctgggagcctggcactgtgagtgccgtgcgccgtgctgggagcct
ggcactgtgagtgccgtgcgccgtgctgggagcctggcactctgagtgccgtgcgccg
tgctgggagcctgtcactgtgagtgccgtgcgccgtgctgggagcctgtcactgtgag
tgccgtgcgccgtgctgggagcctggcactgtgagtgccgtgcgccgtgctgggagcc
tatcactgtgagggccgtgcgctgtgctgggagcctggcactgtgag"
/db_xref="dbSNP:1950641758"
variation 7498
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950644204"
variation 7499
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:1950644192"
variation 7501
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:542365755"
variation 7511..7512
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="gg"
/db_xref="dbSNP:1950644140"
variation 7512..7721
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="gcactgtgagtgccgtgcgccgtgctgggagcctggcactgtgagtgc
cgtgcgccgtgctgggagcctggcactctgagtgccgtgcgccgtgctgggagcctgt
cactgtgagtgccgtgcgccgtgctgggagcctgtcactgtgagtgccgtgcgccgtg
ctgggagcctggcactgtgagtgccgtgcgccgtgctgggagccta"
/db_xref="dbSNP:2543255404"
variation 7512..7544
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="gcactgtgagtgccgtgcgccgtgctgggagcc"
/db_xref="dbSNP:1950643973"
variation 7512
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="gggagcctgtcactgtgagtgccgtgcgccgtgctg"
/db_xref="dbSNP:1555267719"
variation 7512
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:79357308"
variation 7513..7731
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="cactgtgag"
/replace="cactgtgagtgccgtgcgccgtgctgggagcctggcactgtgagtgcc
gtgcgccgtgctgggagcctggcactctgagtgccgtgcgccgtgctgggagcctgtc
actgtgagtgccgtgcgccgtgctgggagcctgtcactgtgagtgccgtgcgccgtgc
tgggagcctggcactgtgagtgccgtgcgccgtgctgggagcctatcactgtgag"
/db_xref="dbSNP:1950642182"
variation 7513..7720
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="cactgtgagtgccgtgcgccgtgctgggagcctggcactgtgagtgcc
gtgcgccgtgctgggagcct"
/replace="cactgtgagtgccgtgcgccgtgctgggagcctggcactgtgagtgcc
gtgcgccgtgctgggagcctggcactctgagtgccgtgcgccgtgctgggagcctgtc
actgtgagtgccgtgcgccgtgctgggagcctgtcactgtgagtgccgtgcgccgtgc
tgggagcctggcactgtgagtgccgtgcgccgtgctgggagcct"
/db_xref="dbSNP:1950642485"
variation 7513..7651
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="cactgtgagtgccgtgcgccgtgctgggagcctg"
/replace="cactgtgagtgccgtgcgccgtgctgggagcctggcactgtgagtgcc
gtgcgccgtgctgggagcctggcactctgagtgccgtgcgccgtgctgggagcctgtc
actgtgagtgccgtgcgccgtgctgggagcctg"
/db_xref="dbSNP:1950643230"
variation 7517
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:866987567"
variation 7518..7616
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="tgagtgccgtgcgccgtgctgggagcctg"
/replace="tgagtgccgtgcgccgtgctgggagcctggcactgtgagtgccgtgcg
ccgtgctgggagcctggcactctgagtgccgtgcgccgtgctgggagcctg"
/db_xref="dbSNP:2543255609"
variation 7522
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="t"
/db_xref="dbSNP:2543255723"
variation 7522
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:71452540"
variation 7523..7741
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="gccgtgcgc"
/replace="gccgtgcgccgtgctgggagcctggcactgtgagtgccgtgcgccgtg
ctgggagcctggcactctgagtgccgtgcgccgtgctgggagcctgtcactgtgagtg
ccgtgcgccgtgctgggagcctgtcactgtgagtgccgtgcgccgtgctgggagcctg
gcactgtgagtgccgtgcgccgtgctgggagcctatcactgtgagggccgtgcgc"
/db_xref="dbSNP:2543255313"
variation 7525
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1246142517"
variation 7526
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1950644052"
variation 7527
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:71452539"
variation 7529
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950644026"
variation 7530
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1950644012"
variation 7532..7701
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="cgtgctgggagcctggcactgtgagtgccgtgcgccgtgctgggagcc
tggcactctgagtgccgtgcgccgtgctgggagcctgtcactgtgagtgccgtgcgcc
gtgctgggagcctgtcactgtgagtgccgtgcgccgtgctgggagcctggcactgtga
gtgccg"
/db_xref="dbSNP:1566167672"
variation 7532
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:868147846"
variation 7533..7766
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="gtgctgggagcctggcactgtgag"
/replace="gtgctgggagcctggcactgtgagtgccgtgcgccgtgctgggagcct
ggcactctgagtgccgtgcgccgtgctgggagcctgtcactgtgagtgccgtgcgccg
tgctgggagcctgtcactgtgagtgccgtgcgccgtgctgggagcctggcactgtgag
tgccgtgcgccgtgctgggagcctatcactgtgagggccgtgcgctgtgctgggagcc
tggcactgtgag"
/db_xref="dbSNP:1950641749"
variation 7533
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:2543255705"
variation 7536
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950643981"
variation 7546..7645
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="ggcactgtgagtgccgtgcgccgtgctgggagcctggcactctgagtg
ccgtgcgccgtgctgggagcctgtcactgtgagtgccgtgcgccgtgctggg"
/db_xref="dbSNP:1566167710"
variation 7546..7547
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="gg"
/db_xref="dbSNP:1444737479"
variation 7546
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1593432484"
variation 7547
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:7953573"
variation 7548..7731
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="cactgtgag"
/replace="cactgtgagtgccgtgcgccgtgctgggagcctggcactctgagtgcc
gtgcgccgtgctgggagcctgtcactgtgagtgccgtgcgccgtgctgggagcctgtc
actgtgagtgccgtgcgccgtgctgggagcctggcactgtgagtgccgtgcgccgtgc
tgggagcctatcactgtgag"
/db_xref="dbSNP:1566167631"
variation 7548..7691
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="cactgtgagtgccgtgcgccgtgctgggagcctggcact"
/replace="cactgtgagtgccgtgcgccgtgctgggagcctggcactctgagtgcc
gtgcgccgtgctgggagcctgtcactgtgagtgccgtgcgccgtgctgggagcctgtc
actgtgagtgccgtgcgccgtgctgggagcctggcact"
/db_xref="dbSNP:1950642904"
variation 7548..7651
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="cactgtgagtgccgtgcgccgtgctgggagcctg"
/replace="cactgtgagtgccgtgcgccgtgctgggagcctggcactctgagtgcc
gtgcgccgtgctgggagcctgtcactgtgagtgccgtgcgccgtgctgggagcctg"
/db_xref="dbSNP:1566167706"
variation 7552
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1355461430"
variation 7553..7616
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="tgagtgccgtgcgccgtgctgggagcctg"
/replace="tgagtgccgtgcgccgtgctgggagcctggcactctgagtgccgtgcg
ccgtgctgggagcctg"
/db_xref="dbSNP:1950643507"
variation 7557..7695
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="tgccgtgcgccgtgctgggagcctggcactctgagtgccgtgcgccgt
gctgggagcctgtcactgtgagtgccgtgcgccgtgctgggagcctgtcactgtgagt
gccgtgcgccgtgctgggagcctggcactgtga"
/db_xref="dbSNP:1566167683"
variation 7557
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:7976332"
variation 7558..7741
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="gccgtgcgc"
/replace="gccgtgcgccgtgctgggagcctggcactctgagtgccgtgcgccgtg
ctgggagcctgtcactgtgagtgccgtgcgccgtgctgggagcctgtcactgtgagtg
ccgtgcgccgtgctgggagcctggcactgtgagtgccgtgcgccgtgctgggagccta
tcactgtgagggccgtgcgc"
/db_xref="dbSNP:1950641966"
variation 7561
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1225735866"
variation 7562
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:1593432469"
variation 7564
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1302992718"
variation 7565
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1357471296"
variation 7566
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1950643807"
variation 7567..7701
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="cgtgctgggagcctggcactctgagtgccgtgcgccgtgctgggagcc
tgtcactgtgagtgccgtgcgccgtgctgggagcctgtcactgtgagtgccgtgcgcc
gtgctgggagcctggcactgtgagtgccg"
/db_xref="dbSNP:1566167667"
variation 7567..7573
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="cgtgctg"
/replace="cgtgctgcgtgctg"
/db_xref="dbSNP:1950643736"
variation 7567
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1423252493"
variation 7568
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1950643778"
variation 7569
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1593432459"
variation 7570
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950643752"
variation 7577
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1950643725"
variation 7578
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1251678689"
variation 7582..7721
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="gcactctgagtgccgtgcgccgtgctgggagcctgtcactgtgagtgc
cgtgcgccgtgctgggagcctgtcactgtgagtgccgtgcgccgtgctgggagcctgg
cactgtgagtgccgtgcgccgtgctgggagccta"
/db_xref="dbSNP:1950642348"
variation 7582
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:10870524"
variation 7583..7726
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="cact"
/replace="cactctgagtgccgtgcgccgtgctgggagcctgtcactgtgagtgcc
gtgcgccgtgctgggagcctgtcactgtgagtgccgtgcgccgtgctgggagcctggc
actgtgagtgccgtgcgccgtgctgggagcctatcact"
/db_xref="dbSNP:1566167633"
variation 7583..7621
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="cact"
/replace="cactctgagtgccgtgcgccgtgctgggagcctgtcact"
/db_xref="dbSNP:1950643445"
variation 7586..7587
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="gtgagtgccgtgcgccgtgctgggagcctggca"
/db_xref="dbSNP:2136897181"
variation 7587
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:28558381"
variation 7588..7686
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="tgagtgccgtgcgccgtgctgggagcctg"
/replace="tgagtgccgtgcgccgtgctgggagcctgtcactgtgagtgccgtgcg
ccgtgctgggagcctg"
/replace="tgagtgccgtgcgccgtgctgggagcctgtcactgtgagtgccgtgcg
ccgtgctgggagcctgtcactgtgagtgccgtgcgccgtgctgggagcctg"
/db_xref="dbSNP:1566167688"
variation 7588..7616
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="tgagtgccgtgcgccgtgctgggagcctg"
/replace="tgagtgccgtgcgccgtgctgggagcctggcactgtgagtgccgtgcg
ccgtgctgggagcctg"
/db_xref="dbSNP:1950643491"
variation 7588..7589
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="tg"
/replace="tgtg"
/db_xref="dbSNP:2136897171"
variation 7588
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="t"
/replace="tt"
/db_xref="dbSNP:1950643623"
variation 7592
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:878879349"
variation 7595
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1429890265"
variation 7597
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:2543255627"
variation 7599
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2543255626"
variation 7601
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950643592"
variation 7602..7608
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="cgtgctg"
/db_xref="dbSNP:1950643532"
variation 7602
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950643578"
variation 7603..7756
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="gtgctgggagcctg"
/replace="gtgctgggagcctgtcactgtgagtgccgtgcgccgtgctgggagcct
gtcactgtgagtgccgtgcgccgtgctgggagcctggcactgtgagtgccgtgcgccg
tgctgggagcctatcactgtgagggccgtgcgctgtgctgggagcctg"
/db_xref="dbSNP:1950641817"
variation 7603
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1950643560"
variation 7607
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1164239695"
variation 7608
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1167847888"
variation 7609
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950643516"
variation 7616..7617
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="gcactctgagtgccgtgcgccgtgctgggagcc"
/db_xref="dbSNP:1950643482"
variation 7617..7716
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="tcactgtgagtgccgtgcgccgtgctgggagcctgtcactgtgagtgc
cgtgcgccgtgctgggagcctggcactgtgagtgccgtgcgccgtgctggga"
/db_xref="dbSNP:2543255433"
variation 7617..7650
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="tcactgtgagtgccgtgcgccgtgctgggagcct"
/db_xref="dbSNP:1950643264"
variation 7617..7618
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="gg"
/db_xref="dbSNP:2543255598"
variation 7617
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:28651415"
variation 7618..7720
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="cactgtgagtgccgtgcgccgtgctgggagcct"
/replace="cactgtgagtgccgtgcgccgtgctgggagcctgtcactgtgagtgcc
gtgcgccgtgctgggagcctggcactgtgagtgccgtgcgccgtgctgggagcct"
/db_xref="dbSNP:1950642474"
variation 7618
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1593432437"
variation 7621
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2543255592"
variation 7622
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1405979894"
variation 7627
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="t"
/db_xref="dbSNP:2543255589"
variation 7627
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:368680522"
variation 7628..7741
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="gccgtgcgc"
/replace="gccgtgcgccgtgctgggagcctgtcactgtgagtgccgtgcgccgtg
ctgggagcctggcactgtgagtgccgtgcgccgtgctgggagcctatcactgtgaggg
ccgtgcgc"
/db_xref="dbSNP:1950641957"
variation 7628..7661
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="gccgtgcgccgtgctgggagcctgtcactgtgag"
/replace="gccgtgcgccgtgctgggagcctgtcactgtgagggccgtgcgccgtg
ctgggagcctgtcactgtgag"
/db_xref="dbSNP:2543255529"
variation 7630
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950643409"
variation 7631
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1950643396"
variation 7632
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:2543255576"
variation 7633..7636
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="gc"
/replace="gcgc"
/db_xref="dbSNP:2543255570"
variation 7633
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1392126872"
variation 7634
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950643372"
variation 7635
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1460988218"
variation 7637..7666
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="cgtgctgggagcctgtcactgtgagtgccg"
/db_xref="dbSNP:1950643103"
variation 7637..7643
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="cgtgctg"
/db_xref="dbSNP:1950643307"
variation 7637
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:113501096"
variation 7638..7756
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="gtgctgggagcctg"
/replace="gtgctgggagcctgtcactgtgagtgccgtgcgccgtgctgggagcct
ggcactgtgagtgccgtgcgccgtgctgggagcctatcactgtgagggccgtgcgctg
tgctgggagcctg"
/db_xref="dbSNP:1950641806"
variation 7638
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="g"
/db_xref="dbSNP:2543255566"
variation 7638
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:534733808"
variation 7641
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950643324"
variation 7644
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1380793372"
variation 7647..7651
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="gcctg"
/db_xref="dbSNP:1566167702"
variation 7651
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950643188"
variation 7652..7731
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="tcactgtgag"
/replace="tcactgtgagtgccgtgcgccgtgctgggagcctggcactgtgagtgc
cgtgcgccgtgctgggagcctatcactgtgag"
/db_xref="dbSNP:1950642155"
variation 7652..7660
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="tcactgtga"
/db_xref="dbSNP:1252269217"
variation 7652
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="t"
/db_xref="dbSNP:1950643172"
variation 7652
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:28655176"
variation 7653..7720
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="cactgtgagtgccgtgcgccgtgctgggagcct"
/replace="cactgtgagtgccgtgcgccgtgctgggagcctggcactgtgagtgcc
gtgcgccgtgctgggagcct"
/replace="cactgtgagtgccgtgcgccgtgctgggagcctggcactgtgagtgcc
gtgcgccgtgctgggagcctggcactgtgagtgccgtgcgccgtgctgggagcct"
/db_xref="dbSNP:1566167644"
variation 7654
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1673499961"
variation 7657
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1470668792"
variation 7659
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2543255534"
variation 7662
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1221522081"
variation 7663..7741
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="gccgtgcgc"
/replace="gccgtgcgccgtgctgggagcctggcactgtgagtgccgtgcgccgtg
ctgggagcctatcactgtgagggccgtgcgc"
/db_xref="dbSNP:1950641950"
variation 7663..7686
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="gccgtgcgccgtgctgggagcctg"
/replace="gccgtgcgccgtgctgggagcctgtcactgtgagggccgtgcgccgtg
ctgggagcctg"
/db_xref="dbSNP:2136897013"
variation 7665
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1271845303"
variation 7666
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:576819015"
variation 7667
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:2543255518"
variation 7668..7673
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="gcgccg"
/db_xref="dbSNP:1950643017"
variation 7668
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1212561134"
variation 7669
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950643060"
variation 7670
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1260850280"
variation 7672..7701
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="cgtgctgggagcctggcactgtgagtgccg"
/db_xref="dbSNP:1566167666"
variation 7672
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:112474658"
variation 7673..7788
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="gtgctgggagc"
/replace="gtgctgggagcctggcactgtgagtgccgtgcgccgtgctgggagcct
atcactgtgagggccgtgcgctgtgctgggagcctggcactgtgagggccgtgcgctg
tgctgggagc"
/db_xref="dbSNP:1950641529"
variation 7673..7766
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="gtgctgggagcctggcactgtgag"
/replace="gtgctgggagcctggcactgtgagtgccgtgcgccgtgctgggagcct
atcactgtgagggccgtgcgctgtgctgggagcctggcactgtgag"
/db_xref="dbSNP:1950641734"
variation 7673
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1475420034"
variation 7679
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1950643005"
variation 7682
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1189718408"
variation 7684
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2543255503"
variation 7686
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1415622088"
variation 7687..7721
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="gcactgtgagtgccgtgcgccgtgctgggagccta"
/db_xref="dbSNP:1566167641"
variation 7687
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:113408396"
variation 7688..7731
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="cactgtgag"
/replace="cactgtgagtgccgtgcgccgtgctgggagcctatcactgtgag"
/db_xref="dbSNP:1566167629"
variation 7688
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1159715866"
variation 7690
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950642920"
variation 7691..7694
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="tg"
/replace="tgtg"
/db_xref="dbSNP:1451719588"
variation 7692
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1347078997"
variation 7694
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1950642871"
variation 7697
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="t"
/db_xref="dbSNP:1315822101"
variation 7697
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:28542126"
variation 7698..7741
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="gccgtgcgc"
/replace="gccgtgcgccgtgctgggagcctatcactgtgagggccgtgcgc"
/db_xref="dbSNP:1950641933"
variation 7698..7720
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="gccgtgcgccgtgctgggagcct"
/replace="gccgtgcgccgtgctgggagcctggcactgtgagggccgtgcgccgtg
ctgggagcct"
/db_xref="dbSNP:1950642441"
variation 7699
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1376234625"
variation 7700..7769
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="cgtgcgccgtgctgggagcctatcactgtgagggccgtgcgctgtgct
gggagcctggcactgtgagggc"
/db_xref="dbSNP:2543255242"
variation 7700..7734
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="cgtgcgccgtgctgggagcctatcactgtgagggc"
/db_xref="dbSNP:879591782"
variation 7700
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950642799"
variation 7701
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:111628027"
variation 7702
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950642718"
variation 7703..7708
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="gcgccg"
/db_xref="dbSNP:1283012994"
variation 7703
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950642709"
variation 7704
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1355412164"
variation 7705
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1225105691"
variation 7706..7707
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="ggtgctgggagcctggcactgtgagggccgtgcg"
/replace="ggtgctgggagcctggcactgtgagtgccctgcg"
/replace="tgtgctgggagcctggcactgtgagtgccctgcg"
/db_xref="dbSNP:1566167654"
variation 7706
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1318258337"
variation 7707..7708
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="atgctgggagcctggcactgtgagtgccgtgcgct"
/replace="t"
/db_xref="dbSNP:1373653900"
variation 7707
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:10870522"
variation 7708..7755
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="gtgctgggagcct"
/replace="gtgctgggagcctatcactgtgagggccgtgcgctgtgctgggagcct
"
/replace="gtgctgggagcctatcactgtgagggccgtgcgctgtgctgggagcct
atcactgtgagggccgtgcgctgtgctgggagcct"
/db_xref="dbSNP:1950641832"
variation 7708..7720
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="gtgctgggagcct"
/replace="gtgctgggagcctggcactgtgagggccgtgcgctgtgctgggagcct
"
/replace="gtgctgggagcctggcactgtgagtgccctgcgctgtgctgggagcct
"
/replace="gtgctgggagcctggcactgtgagtgccgtgcgctgtgctgggagcct
"
/replace="gtgctgggagcctgtcactgtgagtgccgtgcgctgtgctgggagcct
"
/replace="gtgctgggagcctgtcactgtgagtgccgtgcgctgtgctgggagcct
ggcactgtgagtgccctgcgctgtgctgggagcct"
/db_xref="dbSNP:rs1566167643"
variation 7708
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1950642567"
variation 7710
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1646338394"
variation 7714
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1593432347"
variation 7715
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1403513576"
variation 7716..7722
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="agcctat"
/db_xref="dbSNP:2543255394"
variation 7716
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1485770703"
variation 7717..7720
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="gcct"
/replace="gcctggcactgtgagtgccgtgcgctgtgctgggcgcct"
/db_xref="dbSNP:1950642400"
variation 7718..7723
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="cctatc"
/db_xref="dbSNP:1950642268"
variation 7719..7742
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="ct"
/replace="ctatcactgtgagggccgtgcgct"
/db_xref="dbSNP:2136896758"
variation 7719..7726
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="ct"
/replace="ctatcact"
/db_xref="dbSNP:202217087"
variation 7719..7720
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="ct"
/replace="ctgggagcctggcactgtgagtgccgtgcgccgtgct"
/db_xref="dbSNP:1555267700"
variation 7720..7721
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="ggcactgtgagggccgtgcgctgtgctggg"
/replace="ggcactgtgagtgccgtgcgctgtgctggg"
/db_xref="dbSNP:1400810489"
variation 7720
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950642380"
variation 7721..7722
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="gcc"
/replace="gcctg"
/db_xref="dbSNP:1566167638"
variation 7721
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:377620361"
variation 7722..7723
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="gg"
/replace="gggagcctgg"
/db_xref="dbSNP:1566167634"
variation 7722
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:373148235"
variation 7723..7788
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="cactgtgagggccgtgcgctgtgctgggagc"
/replace="cactgtgagggccgtgcgctgtgctgggagcctggcactgtgagggcc
gtgcgctgtgctgggagc"
/replace="cactgtgagggccgtgcgctgtgctgggagcctggcactgtgagggcc
gtgcgctgtgctgggagcctggcactgtgagggccgtgcgctgtgctgggagc"
/db_xref="dbSNP:1566167592"
variation 7723..7741
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="cactgtgagggccgtgcgc"
/replace="cactgtgagggccgtgcgccgtgctgggagcctggcactgtgagggcc
gtgcgc"
/db_xref="dbSNP:1950641923"
variation 7723..7731
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="cactgtgag"
/replace="cactgtgagtgccgtgcgctgtgctgggagcctggcactgtgag"
/db_xref="dbSNP:1950642120"
variation 7723
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="ccgtgcgccgtgctgggagcctggc"
/db_xref="dbSNP:2543255381"
variation 7724
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950642244"
variation 7727
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1950642205"
variation 7731..7762
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="gggccgtgcgctgtgctgggagcctggcactg"
/db_xref="dbSNP:2543255264"
variation 7732
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1474740605"
variation 7733
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1304286198"
variation 7734
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:183941859"
variation 7735
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:540115022"
variation 7736
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="g"
/db_xref="dbSNP:879816478"
variation 7736
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:573131732"
variation 7737
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:2543255321"
variation 7739
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:998381998"
variation 7740
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950641979"
variation 7741..7742
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="cgtgctgggagcctggcactgtgagggccg"
/db_xref="dbSNP:1950641907"
variation 7741
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950641912"
variation 7742..7775
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="tgtgctgggagcctggcactgtgagggccgtgcg"
/db_xref="dbSNP:1950641657"
variation 7742
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:61952781"
variation 7743
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1443366307"
variation 7745..7757
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="gctgggagcctgg"
/db_xref="dbSNP:2136896720"
variation 7745
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1950641858"
variation 7748
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:900129462"
variation 7750
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:532183889"
variation 7755
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1039847748"
variation 7756..7757
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="gg"
/db_xref="dbSNP:2136896714"
variation 7756
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:946868656"
variation 7757
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:893976411"
variation 7758..7788
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="cactgtgagggccgtgcgctgtgctgggagc"
/replace="cactgtgagggccgtgcgctgtgctgggagcctgtcactgtgagggcc
gtgcgctgtgctgggagc"
/db_xref="dbSNP:1950641500"
variation 7758
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:2543255271"
variation 7760
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2136896705"
variation 7762
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:564722306"
variation 7764..7768
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="gaggg"
/db_xref="dbSNP:2543255246"
variation 7764
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1950641766"
variation 7766
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2543255253"
variation 7767
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:113258909"
variation 7769
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950641704"
variation 7770
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:549701323"
variation 7771
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="g"
/db_xref="dbSNP:2543255235"
variation 7771
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:531117989"
variation 7772
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:2543255231"
variation 7773
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2136896671"
variation 7774
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1204886586"
variation 7775
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950641645"
variation 7777
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="t"
/db_xref="dbSNP:1250648140"
variation 7777
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:935097835"
variation 7778..7822
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="gtgctgg"
/replace="gtgctgggagcatgcatttgtgagacccgccctgcccagtgctgg"
/db_xref="dbSNP:1950641396"
variation 7778
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:927600966"
variation 7781
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:563983297"
variation 7785
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:947949372"
variation 7787
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:539644826"
variation 7789
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950641490"
variation 7790
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2543255206"
variation 7790
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="t"
/replace="tt"
/db_xref="dbSNP:1950641480"
variation 7791
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1593432296"
variation 7793
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:916462974"
variation 7802
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1593432292"
variation 7805
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:542089538"
variation 7806
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:963215113"
variation 7808
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1394640769"
variation 7810
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2136896596"
variation 7814..7816
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="cag"
/db_xref="dbSNP:1950641405"
variation 7815
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950641418"
variation 7819
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:2136896589"
variation 7822
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2543255200"
variation 7824
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2543255197"
variation 7825
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2543255196"
variation 7826
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2543255192"
variation 7827
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1410881147"
variation 7829
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:886434651"
variation 7831
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:2543255189"
variation 7833
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:10870521"
variation 7834
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:2543255183"
variation 7837
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1950641305"
variation 7839
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1950641296"
variation 7841
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1950641284"
variation 7842
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1217370706"
variation 7843
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1329358138"
variation 7844
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1852593473"
variation 7845
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:2543255167"
variation 7846
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2543255164"
variation 7847
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:191420424"
variation 7848
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:951577619"
variation 7849
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1442448486"
variation 7850
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1029613241"
variation 7851
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2543255154"
variation 7852
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:2543255153"
variation 7854
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2543255149"
variation 7860
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:899217203"
variation 7861
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1326119414"
variation 7862
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1274802723"
variation 7863
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:998182523"
variation 7864
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:964019658"
variation 7865
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:2136896515"
variation 7869
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2543255143"
variation 7870
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1055634862"
variation 7871
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:937170617"
variation 7872
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:2543255138"
variation 7873
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2543255135"
variation 7874
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:541124619"
variation 7875
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950641106"
variation 7877
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:2136896500"
variation 7879
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1191749883"
variation 7881
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:1950641083"
variation 7883
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1950641068"
variation 7885
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1360539655"
variation 7886
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1011592372"
variation 7887..7892
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="ag"
/replace="agaaag"
/db_xref="dbSNP:1950640992"
variation 7887..7889
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="aga"
/db_xref="dbSNP:1431602410"
variation 7888
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1593432252"
variation 7889..7891
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="aaa"
/replace="aaaa"
/db_xref="dbSNP:2136896481"
variation 7889
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1475835864"
variation 7893
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1593432246"
variation 7895..7898
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="ttt"
/replace="tttt"
/replace="ttttt"
/db_xref="dbSNP:1417864380"
variation 7896
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:2136896470"
variation 7899
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1593432241"
variation 7901
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1409745673"
variation 7903
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2543255107"
variation 7904
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:905719840"
variation 7907
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:2543255100"
variation 7908
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:768272207"
variation 7909
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:576880296"
variation 7910
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:2543255093"
variation 7911
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950640890"
variation 7912..7913
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="a"
/db_xref="dbSNP:2543255086"
variation 7913
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1566167556"
variation 7914
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1045615398"
variation 7915
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1950640843"
variation 7918
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1950640818"
variation 7920
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:2136896434"
variation 7921
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950640804"
variation 7922
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950640797"
variation 7927
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950640780"
variation 7932
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1462566195"
variation 7933
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1950640736"
variation 7934
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1950640713"
variation 7935
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1593432223"
variation 7936
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:950010354"
variation 7938
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2543255061"
variation 7939..7940
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="t"
/db_xref="dbSNP:2543255060"
variation 7939
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1330176467"
variation 7940..7941
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="ata"
/db_xref="dbSNP:2543255055"
variation 7940
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1950640656"
variation 7941
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:188008812"
variation 7942
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1053061669"
variation 7944
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:2543255044"
variation 7945
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950640599"
variation 7947
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:999273847"
variation 7948..7949
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="a"
/db_xref="dbSNP:2543255040"
variation 7948
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:543766232"
variation 7950..7952
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="ttc"
/db_xref="dbSNP:1950640533"
variation 7950
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1950640547"
variation 7952..7953
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="ta"
/db_xref="dbSNP:2543255031"
variation 7953
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950640514"
variation 7954
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:2543255028"
variation 7956
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:906320665"
variation 7958..7968
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="tggtctgtctc"
/db_xref="dbSNP:2543255015"
variation 7960
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1336802435"
variation 7961
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:2543255022"
variation 7965
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:925703590"
variation 7967
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1046181547"
variation 7968
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:947667894"
variation 7969
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:916262428"
variation 7970
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:1240561665"
variation 7972..7982
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="ggc"
/replace="ggctcgtgggc"
/db_xref="dbSNP:2136896343"
variation 7976
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1187722441"
variation 7977
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1037601595"
variation 7978
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1593432193"
variation 7981
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:576279302"
variation 7984
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1164810847"
variation 7987
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2543255005"
variation 7988
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1242080706"
variation 7990
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:950909071"
variation 7991..7993
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="ctt"
/db_xref="dbSNP:1319891412"
variation 7992
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2543255001"
variation 7995
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1950639898"
variation 7996
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:747012753"
variation 7998
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2136896318"
variation 7999
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:149842676"
variation 8001
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:994823717"
variation 8003
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1325326383"
variation 8004
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:983725882"
variation 8005
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950639826"
variation 8006
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1283522863"
variation 8007
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1256923722"
variation 8010..8011
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="t"
/replace="tt"
/db_xref="dbSNP:1282429688"
variation 8010
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1033755675"
variation 8014
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1950639736"
variation 8016
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1488064675"
variation 8018
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1002732692"
variation 8019
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1227221545"
variation 8021
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:536484358"
variation 8022
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:866248758"
variation 8023
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:905693355"
variation 8028
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1470199733"
variation 8029
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:11147101"
variation 8032
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2543254932"
variation 8033
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:553954503"
variation 8036
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1670558762"
variation 8044
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1382149058"
variation 8046
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:2543254926"
variation 8047
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:976816028"
variation 8048
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:61952780"
variation 8052
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950639273"
variation 8056
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950639254"
variation 8057
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:2136896195"
variation 8058
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1377114487"
variation 8060
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2543254915"
variation 8063
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1454750599"
variation 8064
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1333446028"
variation 8067
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:571277098"
variation 8069
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1241317563"
variation 8076
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1277803851"
variation 8079
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2543254902"
variation 8080
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:935662855"
variation 8084
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950639088"
variation 8087
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950639070"
variation 8090..8093
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="tcat"
/replace="tcatcat"
/db_xref="dbSNP:1303162508"
variation 8094..8114
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="ttta"
/replace="tttatcttaatcacctcttta"
/db_xref="dbSNP:1200166825"
variation 8097
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:925640631"
variation 8100
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:549524620"
variation 8102..8103
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="aa"
/db_xref="dbSNP:1950638972"
variation 8105
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1282739271"
variation 8107
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:958565565"
variation 8110
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1031164852"
variation 8117
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1172459431"
variation 8118
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1950638878"
variation 8120
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:778731139"
variation 8123
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2136896114"
variation 8124
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1235870907"
variation 8127
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1450072020"
variation 8128
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:906708054"
variation 8129
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1173941110"
variation 8134
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1046150967"
variation 8135
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1432635004"
variation 8140
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1171741871"
variation 8141
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:911649118"
variation 8143
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1012022942"
variation 8144
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1462361547"
variation 8145
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1256451672"
variation 8148
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2136896072"
variation 8150
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:987607744"
variation 8153
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:1950638604"
variation 8155
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:1950638585"
variation 8159
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2136896065"
variation 8160
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2543254842"
variation 8161
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1305921690"
variation 8163
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1368992518"
variation 8164
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:770999360"
variation 8165
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:183812600"
variation 8166
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950638483"
variation 8167
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1341886211"
variation 8168
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1479867316"
variation 8172
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1037803502"
variation 8174
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:941951950"
variation 8175
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:2543254825"
variation 8176
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:974090502"
variation 8179
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1206486819"
variation 8180
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1456934336"
variation 8183
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:4758908"
variation 8184
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1431052783"
variation 8186
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950638267"
variation 8192
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:146620276"
variation 8193
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1832500759"
variation 8195
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1566167428"
variation 8196
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:933124471"
variation 8201
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2543254792"
variation 8202
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1002213139"
variation 8203
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1463316341"
variation 8208
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:144390272"
variation 8208
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="t"
/replace="tt"
/db_xref="dbSNP:1706720898"
variation 8213
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:976784917"
variation 8218..8219
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="gt"
/db_xref="dbSNP:2543254789"
variation 8220
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950638115"
variation 8222
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:2543254787"
variation 8227
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950638101"
variation 8231
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950638085"
variation 8236
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1399362071"
variation 8244
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1025028503"
variation 8246
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1368839147"
variation 8249
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1386472714"
variation 8250
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950637995"
variation 8251
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:2136895967"
variation 8252
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2543254770"
variation 8253
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950637983"
variation 8256
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950637963"
variation 8258
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:559525007"
variation 8260
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2543254762"
variation 8262
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1014019182"
variation 8264..8267
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="ct"
/replace="ctct"
/db_xref="dbSNP:1950637851"
variation 8264
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1225614380"
variation 8266
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1278136580"
variation 8270
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1336040395"
variation 8271
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:942815306"
variation 8273
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1950637781"
variation 8276
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:2136895932"
variation 8279
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:911216767"
variation 8280
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:989925381"
variation 8281
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:958066311"
variation 8284
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:752894969"
variation 8285
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1031636353"
variation 8289
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:201409137"
variation 8290
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:139235080"
variation 8291
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950637669"
variation 8292
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:2136895906"
variation 8302
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950637656"
variation 8303
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:1025173089"
variation 8304
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:929445136"
variation 8306
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1950637589"
variation 8312..8320
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="gttt"
/replace="gttttgttt"
/db_xref="dbSNP:1387341665"
variation 8314..8323
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="tttgtt"
/replace="tttgtttgtt"
/db_xref="dbSNP:1380907060"
variation 8317
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:919459013"
variation 8319..8329
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="ttgttgtt"
/replace="ttgttgttgtt"
/db_xref="dbSNP:1297928499"
variation 8328..8330
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="tt"
/replace="ttt"
/db_xref="dbSNP:1950637537"
variation 8329
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:2543254710"
variation 8330
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:1011990566"
variation 8332
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1950637516"
variation 8335
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:894932964"
variation 8337
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1291961012"
variation 8340
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1180667732"
variation 8342
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:192156529"
variation 8344
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950637478"
variation 8346
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950637467"
variation 8347
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1243344736"
variation 8348
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:2136895845"
variation 8352
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1593432029"
variation 8354
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950637431"
variation 8361
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1593432028"
variation 8363
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1006264255"
variation 8365
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:112065117"
variation 8366
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1490314622"
variation 8369
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2543254680"
variation 8370
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1593432023"
variation 8371
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950637330"
variation 8378
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:886116796"
variation 8379
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2543254672"
variation 8382
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1262269517"
variation 8384
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="t"
/db_xref="dbSNP:1950637282"
variation 8384
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1593432018"
variation 8386
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1593432016"
variation 8388
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1048081360"
variation 8389
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:188472984"
variation 8390
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1593432015"
variation 8391
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1411450845"
variation 8392
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1423333692"
variation 8393
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1009635955"
variation 8394
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:901670066"
variation 8396
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2543254640"
variation 8399
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1566167380"
variation 8400
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1418142002"
variation 8404
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950637123"
variation 8406
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="aa"
/db_xref="dbSNP:1297794700"
variation 8407
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1566167376"
variation 8409
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:183488831"
variation 8410
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:534223390"
variation 8411
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950637067"
variation 8412
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:542937594"
variation 8415
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:371013975"
variation 8416
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:989588451"
variation 8418
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:1289958982"
variation 8421
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1000037919"
variation 8424
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1344758331"
variation 8426
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1212684105"
variation 8427
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1950636959"
variation 8430
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1950636947"
variation 8436
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:2543254601"
variation 8446
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2543254599"
variation 8447
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950636940"
variation 8449
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1235685642"
variation 8450
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:936639764"
variation 8451
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:923983736"
variation 8452
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2543254580"
variation 8458
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:191333889"
variation 8460
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:978321668"
variation 8465
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1038966897"
variation 8467
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1437889950"
variation 8468
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1158338273"
variation 8470
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1395847162"
variation 8471
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:758519807"
variation 8472
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:970997951"
variation 8477
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1358920968"
variation 8479
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:1950636800"
variation 8481
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:2543254567"
variation 8488
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:185451235"
variation 8491
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1300405111"
variation 8496
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1378562644"
variation 8497
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="a"
/db_xref="dbSNP:1443852540"
variation 8504
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1308096635"
variation 8506
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950636748"
variation 8508
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:2136895679"
variation 8515
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1365200772"
variation 8518
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1220769794"
variation 8519
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:991027098"
variation 8521
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1276291597"
variation 8525
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1311367045"
variation 8526
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1183293202"
variation 8528
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1205201989"
variation 8529
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1950636648"
variation 8531
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1950636635"
variation 8532
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1480315521"
variation 8537
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950636612"
variation 8538
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950636601"
variation 8540
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950636595"
variation 8541
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950636586"
variation 8547
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1267311720"
variation 8548
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:959572401"
variation 8550
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950636542"
variation 8552
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1178030567"
variation 8554..8555
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="c"
/db_xref="dbSNP:1950636518"
variation 8556
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950636503"
variation 8562
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:541494303"
variation 8566
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2136895616"
variation 8568
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950636460"
variation 8571
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:571285622"
variation 8572
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1016396019"
variation 8575
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:150738734"
variation 8576
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:368052446"
variation 8577
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:886083507"
variation 8583
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1593431946"
variation 8586
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1025963462"
variation 8587
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="c"
/db_xref="dbSNP:1950636336"
variation 8587
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:997379005"
variation 8588
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:942224857"
variation 8589
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:537485763"
variation 8591
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="t"
/replace="ttt"
/db_xref="dbSNP:1272701636"
variation 8592
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1438231969"
variation 8595
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1366727499"
variation 8599
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:901805827"
variation 8601
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="gg"
/db_xref="dbSNP:2136895573"
variation 8602
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1950636237"
variation 8603
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1280030142"
variation 8604
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1038930006"
variation 8605
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:2543254497"
variation 8607
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1950636198"
variation 8610
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1322576528"
variation 8612
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1007313078"
variation 8615
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:892982622"
variation 8616
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:111405157"
variation 8618
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1950636125"
variation 8620
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1281212237"
variation 8621
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:113652099"
variation 8622
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1950636063"
variation 8624
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:981070143"
variation 8625
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:58455447"
variation 8631
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:923925307"
variation 8632
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1380055836"
variation 8633
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1477803059"
variation 8635
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1390298999"
variation 8637
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1418020403"
variation 8638
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:988183485"
variation 8639
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1159460144"
variation 8640
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2136895515"
variation 8642
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1321178368"
variation 8645
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:548523904"
variation 8646
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1338127192"
variation 8648
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950635865"
variation 8649
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:949615749"
variation 8650
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950635837"
variation 8652
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1358572226"
variation 8654
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950635815"
variation 8656
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="t"
/replace="tt"
/db_xref="dbSNP:2136895494"
variation 8659
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1950635798"
variation 8664
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950635785"
variation 8665
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1226621144"
variation 8666
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1289461055"
variation 8667
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950635754"
variation 8671
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950635745"
variation 8673..8676
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="ccc"
/replace="cccc"
/db_xref="dbSNP:1950635718"
variation 8675
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1950635731"
variation 8676
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:533536105"
variation 8677
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="g"
/db_xref="dbSNP:1261540812"
variation 8677
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:918136575"
variation 8678
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1488160360"
variation 8681
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1189350364"
variation 8684
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1032438321"
variation 8686..8691
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="aaaaa"
/replace="aaaaaa"
/db_xref="dbSNP:1412655050"
variation 8686
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:991079633"
variation 8687..8688
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="c"
/db_xref="dbSNP:35592985"
variation 8688
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:530337431"
variation 8691
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:2136895440"
variation 8694..8695
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="cc"
/db_xref="dbSNP:1950635596"
variation 8694
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1400970335"
variation 8695
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1965935"
variation 8696..8701
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="aaaaaa"
/replace="aaaaaaa"
/db_xref="dbSNP:1342144080"
variation 8697
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1017923740"
variation 8700
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1399096198"
variation 8701
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1007514077"
variation 8705
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950635517"
variation 8706
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1950635508"
variation 8707
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1248819310"
variation 8708
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:547606164"
variation 8709
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1460202155"
variation 8711
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:959778422"
variation 8712
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:909403743"
variation 8713
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:1593431865"
variation 8715
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1950635421"
variation 8716
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1950635406"
variation 8719
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1284138024"
variation 8723
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1353441401"
variation 8725
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950635376"
variation 8726
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2543254396"
variation 8729
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1211969765"
variation 8733
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1258900598"
variation 8735..8741
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="cagctac"
/db_xref="dbSNP:1950635275"
variation 8735
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1441145980"
variation 8743
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:984932207"
variation 8744
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:532717369"
variation 8745
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1470198072"
variation 8748
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1025932353"
variation 8753
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:1180129502"
variation 8755
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:2543254374"
variation 8757..8761
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="ag"
/replace="aggag"
/db_xref="dbSNP:2136895362"
variation 8759
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950635204"
variation 8761
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1378039564"
variation 8763
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1418891558"
variation 8764
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:867006756"
variation 8769
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1173991596"
variation 8772
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950635157"
variation 8774
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:565269686"
variation 8775
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1566167257"
variation 8776
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:189649461"
variation 8782
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:543887608"
variation 8783
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1451420876"
variation 8794..8815
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="tgaaccgagatcgcaccactgc"
/db_xref="dbSNP:2543254334"
variation 8794
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1593431838"
variation 8797
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1593431827"
variation 8799
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:897540792"
variation 8800
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:965691033"
variation 8803
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1376370692"
variation 8804
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1235516172"
variation 8805
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1037474971"
variation 8806
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1343280399"
variation 8808
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1415435656"
variation 8812
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950634980"
variation 8817
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1017445311"
variation 8818
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1593431815"
variation 8819
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1950634933"
variation 8820
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:531654166"
variation 8821..8845
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="cgcctgggcgacagagcgagactct"
/db_xref="dbSNP:2543254302"
variation 8821
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1419346353"
variation 8822
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:942175926"
variation 8823
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950634880"
variation 8825
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1166679594"
variation 8828
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1451942311"
variation 8829
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1476916157"
variation 8830
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1171928955"
variation 8832
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1950634816"
variation 8833..8836
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="ag"
/replace="agag"
/db_xref="dbSNP:1397052220"
variation 8834
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1950634805"
variation 8837
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1390863657"
variation 8838
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1399597898"
variation 8839
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:2136895247"
variation 8840
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1950634762"
variation 8841
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950634752"
variation 8842
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:2543254304"
variation 8843
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1593431795"
variation 8845..8849
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="tatct"
/db_xref="dbSNP:2543254293"
variation 8845
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1965936"
variation 8846
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1442991070"
variation 8847
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:1245230204"
variation 8848
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:2136895214"
variation 8849
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="t"
/db_xref="dbSNP:1950634681"
variation 8849
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:1211890266"
variation 8850
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="c"
/db_xref="dbSNP:1950634665"
variation 8850
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1442799894"
variation 8851..8871
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="aaaaaaaaa"
/replace="aaaaaaaaaa"
/replace="aaaaaaaaaaaa"
/replace="aaaaaaaaaaaaa"
/replace="aaaaaaaaaaaaaa"
/replace="aaaaaaaaaaaaaaa"
/replace="aaaaaaaaaaaaaaaa"
/replace="aaaaaaaaaaaaaaaaa"
/replace="aaaaaaaaaaaaaaaaaa"
/replace="aaaaaaaaaaaaaaaaaaa"
/replace="aaaaaaaaaaaaaaaaaaaa"
/replace="aaaaaaaaaaaaaaaaaaaaa"
/replace="aaaaaaaaaaaaaaaaaaaaaa"
/replace="aaaaaaaaaaaaaaaaaaaaaaa"
/replace="aaaaaaaaaaaaaaaaaaaaaaaa"
/replace="aaaaaaaaaaaaaaaaaaaaaaaaa"
/replace="aaaaaaaaaaaaaaaaaaaaaaaaaa"
/replace="aaaaaaaaaaaaaaaaaaaaaaaaaaa"
/db_xref="dbSNP:rs60018437"
variation 8861..8862
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="g"
/db_xref="dbSNP:1272093971"
variation 8864..8865
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="g"
/db_xref="dbSNP:1950634635"
variation 8864
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950634646"
variation 8865
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950634614"
variation 8866..8867
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="g"
/db_xref="dbSNP:2031436001"
variation 8868
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1320573190"
variation 8869..8872
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="aaag"
/replace="aaagaaag"
/db_xref="dbSNP:1491475804"
variation 8869
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1593431778"
variation 8870..8880
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="aagcaag"
/replace="aagcaagcaag"
/replace="aagcaagcaagcaag"
/db_xref="dbSNP:1344278040"
variation 8870
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="agca"
/db_xref="dbSNP:1950634574"
variation 8871..8874
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="agca"
/db_xref="dbSNP:1950634520"
variation 8871
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1197269011"
variation 8872..8873
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="gc"
/db_xref="dbSNP:1491304901"
variation 8872
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1593431763"
variation 8873
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1423076470"
variation 8874
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1950634511"
variation 8877
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1194000110"
variation 8882
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1297667258"
variation 8884
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1319438448"
variation 8886..8888
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="aa"
/replace="aaa"
/db_xref="dbSNP:1342747592"
variation 8890
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1950634440"
variation 8896
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950634430"
variation 8897
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1244632359"
variation 8898..8901
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="agga"
/replace="aggaagga"
/db_xref="dbSNP:949678192"
variation 8898
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950634150"
variation 8899
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1950634138"
variation 8900
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1007493202"
variation 8901
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1316752747"
variation 8902..8903
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="gg"
/db_xref="dbSNP:918173476"
variation 8902
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2543254216"
variation 8905
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2543254212"
variation 8908
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1285600817"
variation 8909
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1593431751"
variation 8912
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1353768868"
variation 8914
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:892941701"
variation 8917
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950634052"
variation 8920
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:543000977"
variation 8921
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950634030"
variation 8923
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1177646638"
variation 8925
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:935349824"
variation 8926..8948
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="gaggga"
/replace="gagggatgtgctttgcagaggga"
/db_xref="dbSNP:1566167193"
variation 8926
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:925338183"
variation 8927
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2136895079"
variation 8931
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:1950633989"
variation 8934
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1950633980"
variation 8935
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="g"
/db_xref="dbSNP:1950633968"
variation 8936
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:2136895073"
variation 8940
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1054325575"
variation 8941
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950633947"
variation 8949
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:867932397"
variation 8950
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:968947186"
variation 8953
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1366764467"
variation 8957
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950633850"
variation 8960
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1327352767"
variation 8961
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:779133806"
variation 8962
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1017475519"
variation 8972
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1950633804"
variation 8976
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950633795"
variation 8979
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1432139254"
variation 8985
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:985962954"
variation 8986
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:368817778"
variation 8988
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950633747"
variation 8989
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1030265828"
variation 8990
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950633719"
variation 8991
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:1950633709"
variation 8992
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950633701"
variation 8997
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1356607566"
variation 9002
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950633674"
variation 9004
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:2136895008"
variation 9006
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1593431715"
variation 9008
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1593431712"
variation 9009
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:993139881"
variation 9012
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950633637"
variation 9013
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950633622"
variation 9015
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1314293208"
variation 9017
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1319375824"
variation 9018..9031
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="gccaccagaaggaa"
/db_xref="dbSNP:1950633571"
variation 9018
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1593431708"
variation 9020
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1442858117"
variation 9024
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1243684757"
variation 9032
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1416151852"
variation 9033
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1042500415"
variation 9035
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1950633531"
variation 9037
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950633512"
variation 9042
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1286277700"
variation 9043..9044
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="tg"
/replace="tgtg"
/db_xref="dbSNP:1566167175"
variation 9044
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:949333189"
variation 9051
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1469855398"
variation 9052
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:725067"
variation 9057
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1016414297"
variation 9064
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1183503741"
variation 9065
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1254238074"
variation 9067
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1423316887"
variation 9068
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950633393"
variation 9071
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:2543254128"
variation 9076
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2136894938"
variation 9085
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950633381"
variation 9089
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:1179499443"
variation 9090
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:879529729"
variation 9091
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950633361"
variation 9092
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1483962228"
variation 9094
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1006005295"
variation 9102
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:2136894919"
variation 9107
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2543254109"
variation 9109
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:938303392"
variation 9111
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1275269509"
variation 9112
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1468070358"
variation 9115
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1301590552"
variation 9116
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2136894905"
variation 9120
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1950633268"
variation 9121
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1209762016"
variation 9130
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:545261248"
variation 9138..9139
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="gg"
/db_xref="dbSNP:2543254095"
variation 9142
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950633233"
variation 9145
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:909362045"
variation 9150..9155
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="cccccc"
/replace="ccccccc"
/db_xref="dbSNP:1950633169"
variation 9150
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1950633204"
variation 9152
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:2543254086"
variation 9153
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:368550205"
variation 9154
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1451210220"
variation 9155
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:577761697"
variation 9156
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1291463144"
variation 9157
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1228502298"
variation 9161
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1593431640"
variation 9162
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:1372238398"
variation 9163
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1308324861"
variation 9167
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1278130456"
variation 9168
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1212238594"
variation 9169
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:985014434"
variation 9171
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:1199295515"
variation 9173
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1351602281"
variation 9175..9179
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="tttt"
/replace="ttttt"
/db_xref="dbSNP:2543254062"
variation 9186
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1438108721"
variation 9191
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1178230010"
variation 9192
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1303108642"
variation 9194..9197
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="tcca"
/replace="tccatcca"
/db_xref="dbSNP:1045171510"
variation 9194
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:1426379276"
variation 9195
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1731322770"
variation 9196
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:950950481"
variation 9197
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950632952"
variation 9198
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="g"
/db_xref="dbSNP:1790299030"
variation 9199
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1359046369"
variation 9211
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1468865438"
variation 9212
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1593431609"
variation 9213
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1331493560"
variation 9217
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950632899"
variation 9217
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="t"
/replace="tt"
/db_xref="dbSNP:1950632908"
variation 9218
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950632893"
variation 9222
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1950632884"
variation 9224
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:918972353"
variation 9225
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1950632866"
variation 9226
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:975816530"
variation 9227
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:556033550"
variation 9232
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1444199913"
variation 9235..9238
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="gggg"
/replace="gggggg"
/db_xref="dbSNP:1220684747"
variation 9236
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1278586073"
variation 9237
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1950632802"
variation 9238
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1368049086"
variation 9239
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1348192971"
variation 9248
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1311493793"
variation 9249..9257
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="ca"
/replace="cacccaaca"
/db_xref="dbSNP:2136894774"
variation 9250
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1219132318"
variation 9251
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1017248103"
variation 9252
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:2543254018"
variation 9254
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1260126467"
variation 9256
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1007877682"
variation 9257
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950632711"
variation 9258..9259
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="g"
/db_xref="dbSNP:2136894770"
variation 9258
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1456486260"
variation 9260
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:896716441"
variation 9261
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:533379840"
variation 9267
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950632655"
variation 9269
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1489686071"
variation 9270
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1189806728"
variation 9273
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950632620"
variation 9276
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1424866842"
variation 9279
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1478465267"
variation 9284
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1173441240"
variation 9286
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950632512"
variation 9287
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1950632505"
variation 9289
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1165656988"
variation 9290
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1425232866"
variation 9293
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1463547347"
variation 9298
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950632461"
variation 9299
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950632447"
variation 9304
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:754400291"
variation 9309
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950632421"
variation 9312
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1950632411"
variation 9315
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:998660832"
variation 9317
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:184936353"
variation 9320
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1350057445"
variation 9321
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2136894714"
variation 9322
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1950632362"
variation 9323
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950632351"
variation 9328
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1400328673"
variation 9329
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:554960578"
variation 9331
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1156601953"
variation 9334
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1473468165"
variation 9337
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950632282"
variation 9342
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="g"
/db_xref="dbSNP:1280007906"
variation 9348
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1950632263"
variation 9354
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:935313610"
variation 9357..9358
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="cc"
/db_xref="dbSNP:1290902344"
variation 9357
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1213997530"
variation 9358
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950632104"
variation 9359
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:765662190"
variation 9360
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:370328559"
variation 9361
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2543253930"
variation 9363
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1798244521"
variation 9365
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950632068"
variation 9371
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:925339347"
variation 9373
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1198571885"
variation 9376
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1219622923"
variation 9380
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1246554143"
variation 9383
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:979920790"
variation 9384
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:533516831"
variation 9385
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950631983"
variation 9393..9397
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="aaaga"
/db_xref="dbSNP:1950631941"
variation 9393..9395
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="aaa"
/db_xref="dbSNP:545767975"
variation 9394
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950631972"
variation 9398
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950631930"
variation 9400
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1476568905"
variation 9401
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1021023235"
variation 9406
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1413845439"
variation 9409
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1315897901"
variation 9410
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:11147100"
variation 9412
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1230573463"
variation 9416
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950631815"
variation 9422
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1364801864"
variation 9423
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1330219174"
variation 9425..9431
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="ccac"
/replace="ccaccac"
/db_xref="dbSNP:1429903872"
variation 9425
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:896472197"
variation 9426
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950631767"
variation 9428
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1950631757"
variation 9429
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1950631731"
variation 9430
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1593431505"
variation 9431
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1055164292"
variation 9432
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:756849208"
variation 9435
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:887995119"
variation 9436
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1370436060"
variation 9437
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1049784452"
variation 9439
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:182209111"
variation 9440
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1006303841"
variation 9441
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:919443646"
variation 9442
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1219188695"
variation 9448
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950631589"
variation 9451
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1316635339"
variation 9454
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:969132479"
variation 9458
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950631546"
variation 9459
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1023356207"
variation 9463
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1950631521"
variation 9466
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950631506"
variation 9469
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:1013685769"
variation 9471
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1188827984"
variation 9474
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1237606930"
variation 9475
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:1950631469"
variation 9477
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1473488786"
variation 9478
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950631447"
variation 9479
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950631438"
variation 9480
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:975785488"
variation 9481..9483
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="ccc"
/replace="cccc"
/db_xref="dbSNP:1950631419"
variation 9487
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:144150293"
variation 9491
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1950631389"
variation 9492
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1950631371"
variation 9493
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:910211187"
variation 9494
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950631357"
variation 9495
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950631347"
variation 9496
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:540668464"
variation 9497
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1160280661"
variation 9498..9499
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="aa"
/db_xref="dbSNP:1950631300"
variation 9499
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:762506347"
variation 9500
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:746534310"
variation 9503
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950631272"
variation 9513
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1400109467"
variation 9518
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:957266472"
variation 9529
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950631247"
variation 9530
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1334745075"
variation 9538
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:999819250"
variation 9539
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1032897054"
variation 9542
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1314662445"
variation 9550
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1593431461"
variation 9551
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:977757026"
variation 9553
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1950631164"
variation 9556
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2543253817"
variation 9557
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950631153"
variation 9558
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:967183171"
variation 9559
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1307591424"
variation 9560
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950631117"
variation 9561
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2136894480"
variation 9564
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="cc"
/db_xref="dbSNP:1350393520"
variation 9566
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1281256416"
variation 9568
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1950631078"
variation 9571
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1470187397"
variation 9573
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2136894468"
variation 9576
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1024171558"
variation 9577
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1175522247"
variation 9579
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1013666792"
variation 9580
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:563815232"
variation 9582
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950631006"
variation 9584
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2136894450"
variation 9585
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1230765206"
variation 9587
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950630974"
variation 9595
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:942707903"
variation 9597
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:911285889"
variation 9599
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950630944"
variation 9603
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1431353311"
variation 9608
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:190443816"
variation 9609
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1950630908"
variation 9611
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1051204564"
variation 9612
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:374909665"
variation 9614
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950630857"
variation 9616
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1950630840"
variation 9620
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2543253775"
variation 9622
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1412870419"
variation 9627
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1336204933"
variation 9631
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950630818"
variation 9633
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:185210452"
variation 9634
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1191198779"
variation 9637
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1034181406"
variation 9638
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:972389157"
variation 9642
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2543253750"
variation 9643
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:961950082"
variation 9645
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950630666"
variation 9655
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:909131501"
variation 9663
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950630640"
variation 9665
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1950630621"
variation 9668
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2543253747"
variation 9670
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950630610"
variation 9674
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1343439692"
variation 9681
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1593431405"
variation 9682
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1002175493"
variation 9685
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="c"
/db_xref="dbSNP:2136894365"
variation 9685
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1245725439"
variation 9687
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:887787164"
variation 9688
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1049293578"
variation 9691
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1950630491"
variation 9693
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1023325114"
variation 9696
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1465122666"
variation 9698
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:752592126"
variation 9699
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950630458"
variation 9710
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950630443"
variation 9711
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1013319826"
variation 9712
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950630414"
variation 9713
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1199259770"
variation 9714
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1950630401"
variation 9717
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950630392"
variation 9725
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:181805118"
variation 9730
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:61952779"
variation 9732
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950630327"
variation 9733
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1593431372"
variation 9735
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="a"
/db_xref="dbSNP:1950630303"
variation 9735
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:76099447"
variation 9736..9758
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="ttcctttt"
/replace="ttccttttttttcttttcctttt"
/db_xref="dbSNP:1950630190"
variation 9739
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1593431366"
variation 9743
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950630260"
variation 9744
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:7970600"
variation 9747
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1359928448"
variation 9748..9759
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="cttttc"
/replace="cttttccttttc"
/db_xref="dbSNP:2136894270"
variation 9754
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2136894279"
variation 9756..9762
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="ttt"
/replace="tttcttt"
/db_xref="dbSNP:1395979731"
variation 9760..9766
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="tttttt"
/replace="ttttttt"
/replace="tttttttt"
/db_xref="dbSNP:1566166967"
variation 9765
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950630165"
variation 9770
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950630139"
variation 9774
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950630128"
variation 9775
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950630114"
variation 9777
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2136894245"
variation 9779
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:577815451"
variation 9781
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1326007033"
variation 9783
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:545792207"
variation 9785
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1279317206"
variation 9786
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950630037"
variation 9788
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950630024"
variation 9789
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1006873480"
variation 9794
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:562712877"
variation 9796
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:935653154"
variation 9799..9815
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="ggc"
/replace="ggctggagggcagtggc"
/db_xref="dbSNP:1269269450"
variation 9799
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:889820400"
variation 9802
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:773162986"
variation 9804
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2136894204"
variation 9807..9815
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="ggc"
/replace="ggcagtggc"
/db_xref="dbSNP:1566166951"
variation 9807
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:2543253670"
variation 9808
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950629968"
variation 9809
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1338394832"
variation 9813
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:2543253668"
variation 9814
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1464357286"
variation 9815
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:925630742"
variation 9819
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1051173498"
variation 9820
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2136894173"
variation 9821
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:2136894166"
variation 9829
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:540771060"
variation 9830
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1555267574"
variation 9831
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950629863"
variation 9836
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:574650870"
variation 9839
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1478856160"
variation 9840
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1287269861"
variation 9842
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:2543253625"
variation 9843
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1458657866"
variation 9844
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2136894130"
variation 9846
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1165218456"
variation 9847
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1024140443"
variation 9850
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950629767"
variation 9851
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1950629755"
variation 9856
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1950629741"
variation 9864
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1950629727"
variation 9865
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:2543253594"
variation 9869
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1364107304"
variation 9873
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950629701"
variation 9875
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:375024869"
variation 9878
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:772396731"
variation 9884
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:958534491"
variation 9886
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1033739352"
variation 9888..9890
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="ggg"
/replace="gggg"
/db_xref="dbSNP:1325334189"
variation 9889
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1002716448"
variation 9890
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:748332566"
variation 9895
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:985137948"
variation 9898
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1950629585"
variation 9901
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1266773456"
variation 9905
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:952061156"
variation 9909
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:969015945"
variation 9913
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1221396286"
variation 9920
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2543253540"
variation 9921
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:1950629525"
variation 9923
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:575065160"
variation 9928
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1242152402"
variation 9929
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="t"
/replace="tt"
/db_xref="dbSNP:2543253535"
variation 9934
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:993703230"
variation 9935
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950629469"
variation 9939
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1261212346"
variation 9940
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:960409097"
variation 9945
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1593431267"
variation 9947
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950629422"
variation 9948
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1950629402"
variation 9949
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:898123032"
variation 9951
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:778622706"
variation 9956
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1383572440"
variation 9965
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1199052981"
variation 9970
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1593431258"
variation 9971
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1484455735"
variation 9973
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1031156856"
variation 9975
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1257004115"
variation 9981
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1950629298"
variation 9983
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1444441204"
variation 9985
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950629276"
variation 9986
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1950629256"
variation 9990
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1159673966"
variation 9993
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1040608111"
variation 9994
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:768933287"
variation 9995
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:978309114"
variation 9997
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:749620523"
variation 10001
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1050160853"
variation 10002
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:780753580"
variation 10018
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1950629179"
variation 10022
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:555023559"
variation 10026
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950629156"
variation 10027
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:373611946"
variation 10028
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950629137"
variation 10030
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950629126"
variation 10032
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:2543253480"
variation 10033
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1380071233"
variation 10034
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1022558198"
variation 10035
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:533576088"
variation 10039
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1382218120"
variation 10040
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:925631215"
variation 10041
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1950629068"
variation 10043
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1566166897"
variation 10044
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="aa"
/db_xref="dbSNP:34393392"
variation 10048
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:889792832"
variation 10049
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1202213279"
variation 10052
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1041367634"
variation 10053
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:998178278"
variation 10057..10063
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="ctt"
/replace="cttactt"
/db_xref="dbSNP:1950628930"
variation 10059
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:1950628983"
variation 10061
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1593431207"
variation 10062
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1950628943"
variation 10069
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1179483538"
variation 10070
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:945693864"
variation 10071
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1381034964"
variation 10072
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1417631383"
variation 10074
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:917206315"
variation 10077
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1378665267"
variation 10079
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:143686086"
variation 10080
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1338179064"
variation 10081
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:940551243"
variation 10082..10085
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="gaga"
/replace="gagaga"
/db_xref="dbSNP:1950628788"
variation 10082
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1451552469"
variation 10083
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="aca"
/db_xref="dbSNP:2543253433"
variation 10086
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950628773"
variation 10087
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:372743888"
variation 10090
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1950628745"
variation 10095
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950628737"
variation 10096
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950628725"
variation 10100
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1048976793"
variation 10103
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:958552550"
variation 10104
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:756655332"
variation 10106
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:916491427"
variation 10108
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:2543253405"
variation 10113
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1169867711"
variation 10114..10119
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="agc"
/replace="agcagc"
/db_xref="dbSNP:1566166860"
variation 10119
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:370904373"
variation 10120
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1363005078"
variation 10121
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:939003108"
variation 10126
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:980893171"
variation 10133
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1479873573"
variation 10134
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950628563"
variation 10138
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1268457022"
variation 10139
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950628537"
variation 10140
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1435473603"
variation 10143
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2136893787"
variation 10144
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1184930985"
variation 10146
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:978216519"
variation 10147
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950628493"
variation 10148..10158
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="tctt"
/replace="tcttgactctt"
/db_xref="dbSNP:1950628406"
variation 10149
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="c"
/db_xref="dbSNP:1425229080"
variation 10152
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:751178845"
variation 10154..10157
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="ct"
/replace="ctct"
/db_xref="dbSNP:1170976798"
variation 10154
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:952192641"
variation 10155..10161
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="tct"
/replace="tctttct"
/db_xref="dbSNP:137989222"
variation 10158
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:539320782"
variation 10159
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950628385"
variation 10161
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950628364"
variation 10165
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:954310677"
variation 10167..10171
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="ct"
/replace="cttct"
/db_xref="dbSNP:1950628326"
variation 10167
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950628337"
variation 10169
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1368028373"
variation 10172
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1406770925"
variation 10175
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:2543253349"
variation 10177
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1277399619"
variation 10180
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1566166821"
variation 10189
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2543253345"
variation 10190
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1950628279"
variation 10193
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1027657313"
variation 10195
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1593431131"
variation 10198
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:777131765"
variation 10203
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1950628220"
variation 10205
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950628211"
variation 10209
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1358840481"
variation 10214
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:1950628190"
variation 10216
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1263803034"
variation 10218
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1950628166"
variation 10219
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:571805769"
variation 10229
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1219272478"
variation 10231
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1260266764"
variation 10238
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950628126"
variation 10240
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:897121704"
variation 10246
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:377459548"
variation 10248
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1204067485"
variation 10250
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="cc"
/db_xref="dbSNP:35119550"
variation 10250
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950628073"
variation 10253
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1015690022"
variation 10254
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:2543253306"
variation 10255
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1019182735"
variation 10260
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950628020"
variation 10264
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1006013879"
variation 10265
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1268740992"
variation 10266
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1479842964"
variation 10270
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1009083290"
variation 10276
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950627960"
variation 10280
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:550363707"
variation 10281
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1050999671"
variation 10284
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:888538344"
variation 10285
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1049403531"
variation 10287
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:999953565"
variation 10290
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1301236521"
variation 10295
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1344751674"
variation 10302
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950627878"
variation 10303..10307
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="ctc"
/replace="ctctc"
/db_xref="dbSNP:895092284"
variation 10304
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1950627865"
variation 10306
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2136893566"
variation 10307
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:114780753"
variation 10308
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1041482100"
variation 10309
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1950627813"
variation 10310
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950627803"
variation 10311
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1313093507"
variation 10312
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:757863592"
variation 10315
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1408996971"
variation 10316
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1362071903"
variation 10321
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1950627732"
variation 10323..10339
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="ccagttttattttcttt"
/db_xref="dbSNP:1950627654"
variation 10327..10335
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="tttt"
/replace="ttttatttt"
/db_xref="dbSNP:1950627683"
variation 10327..10330
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="ttt"
/replace="tttt"
/db_xref="dbSNP:1056286917"
variation 10331
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:752327999"
variation 10334..10338
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="tt"
/replace="ttctt"
/db_xref="dbSNP:1291461902"
variation 10334
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1950627695"
variation 10336
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:945725341"
variation 10341
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1950627643"
variation 10343
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:1950627636"
variation 10344..10345
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="tga"
/db_xref="dbSNP:2543253249"
variation 10347
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:2543253247"
variation 10349
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="aa"
/db_xref="dbSNP:939034244"
variation 10350
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2543253245"
variation 10351..10353
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="cgc"
/db_xref="dbSNP:2543253239"
variation 10351
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:764898928"
variation 10352
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:759378370"
variation 10368
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1950627589"
variation 10370
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1243414004"
variation 10371
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950627569"
variation 10374
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1473518473"
variation 10379
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1185584348"
variation 10380
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1057090676"
variation 10381
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2543253230"
variation 10384
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1309799069"
variation 10391
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:2543253224"
variation 10392..10394
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="aa"
/replace="aaa"
/db_xref="dbSNP:2543253222"
variation 10394
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:567786400"
variation 10396
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:937226908"
variation 10397
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1410407845"
variation 10399
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950627465"
variation 10402..10407
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="ccccc"
/replace="cccccc"
/replace="ccccccc"
/db_xref="dbSNP:1343523701"
variation 10403
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:927156575"
variation 10405
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1364707900"
variation 10407
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1420292903"
variation 10408..10409
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="a"
/db_xref="dbSNP:1364374832"
variation 10408
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1564647"
variation 10411
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1161017162"
variation 10412
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:946497615"
variation 10414
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:914989287"
variation 10416
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:1314866593"
variation 10417..10440
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="atagtgctgggctcgcgtaaggca"
/db_xref="dbSNP:1950627123"
variation 10418
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:985653742"
variation 10419
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2136893376"
variation 10420
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1950627278"
variation 10428
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1459108957"
variation 10430
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1368697822"
variation 10431
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1466508"
variation 10432
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1214403408"
variation 10433
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:920712888"
variation 10434
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="t"
/replace="tt"
/db_xref="dbSNP:1462414604"
variation 10435
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:976971389"
variation 10437
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1384449375"
variation 10438
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1440003692"
variation 10439
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:972108446"
variation 10453
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:757032485"
variation 10457
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:1016052898"
variation 10458
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1950627080"
variation 10463
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:114465310"
variation 10464
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:551447791"
variation 10465
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1490350101"
variation 10467
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:147416333"
variation 10468
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1336251371"
variation 10480
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1378132990"
variation 10481
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1950626992"
variation 10484
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1241556786"
variation 10488
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950626955"
variation 10490
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1211731021"
variation 10497
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2136893267"
variation 10499
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1357240788"
variation 10504
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950626914"
variation 10505
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:562613660"
variation 10506
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1022987749"
variation 10510
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1325066883"
variation 10512
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950626863"
variation 10513
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:953719912"
variation 10516
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2543253132"
variation 10519
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950626836"
variation 10520
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1566166729"
variation 10521
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1566166726"
variation 10527
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1950626800"
variation 10532
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950626792"
variation 10533
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1201388368"
variation 10535
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950626769"
variation 10536..10537
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="gg"
/db_xref="dbSNP:1950626755"
variation 10539
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:2136893211"
variation 10543..10545
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="aa"
/replace="aaa"
/db_xref="dbSNP:1950626747"
variation 10547
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950626729"
variation 10550
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1029246459"
variation 10553
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1242080444"
variation 10554
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1260395842"
variation 10555
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950626694"
variation 10558
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1183773076"
variation 10559..10571
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="tgaaaaggcgtca"
/db_xref="dbSNP:2136893153"
variation 10559..10560
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="ttttttttc"
/db_xref="dbSNP:1950626671"
variation 10560..10562
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="gaa"
/db_xref="dbSNP:1950626661"
variation 10560
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:2136893185"
variation 10562..10563
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="ttgttc"
/replace="tttttc"
/db_xref="dbSNP:2136893174"
variation 10562
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:2136893176"
variation 10565..10566
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="ttgaa"
/db_xref="dbSNP:2136893170"
variation 10566..10571
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="gcgtca"
/db_xref="dbSNP:1950626595"
variation 10567..10572
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="cgtcac"
/db_xref="dbSNP:2136893141"
variation 10567
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1227503778"
variation 10568..10569
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="gt"
/db_xref="dbSNP:1950626618"
variation 10568
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:188864935"
variation 10570
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950626607"
variation 10571..10572
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="ag"
/replace="g"
/db_xref="dbSNP:1950626579"
variation 10575..10576
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="aa"
/db_xref="dbSNP:1012054523"
variation 10578
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950626544"
variation 10579
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:760594403"
variation 10580
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1290025891"
variation 10581
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1228926343"
variation 10583
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:781396062"
variation 10585
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950626488"
variation 10586
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1564648"
variation 10587
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:772050348"
variation 10589
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:955066891"
variation 10595..10597
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="cc"
/replace="ccc"
/db_xref="dbSNP:1950626412"
variation 10595
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950626438"
variation 10596
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1950626429"
variation 10603
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:1950626402"
variation 10608
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950626390"
variation 10609
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1003375692"
variation 10612
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:902424970"
variation 10614
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1020071277"
variation 10615
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950626334"
variation 10620
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950626324"
variation 10628
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950626309"
variation 10629
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950626300"
variation 10630
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1593430871"
variation 10631
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950626276"
variation 10638
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1009966820"
variation 10639
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1390951357"
variation 10641
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:895498408"
variation 10645
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1042479727"
variation 10646
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1950626212"
variation 10647
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1950626203"
variation 10649
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1197169522"
variation 10656
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:1950626194"
variation 10657
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1950626182"
variation 10659
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1319492763"
variation 10660
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2170636"
variation 10662
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1414651588"
variation 10665
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:774457560"
variation 10666
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:905814663"
variation 10667
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1479513450"
variation 10673..10697
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="gggatagggagtgaatgcaagaagg"
/replace="gggatagggagtgaatgcaagaagggatagggagtgaatgcaagaagg
"
/db_xref="dbSNP:1480364549"
variation 10673
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1950626104"
variation 10674
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1198835254"
variation 10680
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950626085"
variation 10683
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950626075"
variation 10684
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:561486335"
variation 10687
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:755133713"
variation 10689
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:768976795"
variation 10697
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1463772076"
variation 10699
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1376437491"
variation 10704
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1406261130"
variation 10706
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1305511031"
variation 10711
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950625960"
variation 10713
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:914996891"
variation 10714
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1404855612"
variation 10715
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1702829091"
variation 10723
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:74638608"
variation 10724
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:184084837"
variation 10727
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:749708601"
variation 10729
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="c"
/db_xref="dbSNP:1950625880"
variation 10732..10737
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="gg"
/replace="ggttgg"
/db_xref="dbSNP:932816956"
variation 10738
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1566166664"
variation 10745
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="gtagcccctctcgctcgaacg"
/db_xref="dbSNP:1950625841"
variation 10747
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1267990112"
variation 10748
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1338535859"
variation 10749
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950625807"
variation 10751
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:557741726"
variation 10754..10757
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="ctct"
/replace="ctctct"
/db_xref="dbSNP:2543252963"
variation 10754
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950625786"
variation 10756
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:918399510"
variation 10761
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1489852586"
variation 10762
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:976918914"
variation 10766
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1262597705"
variation 10770
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950625730"
variation 10774
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:142798479"
variation 10775
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1372670412"
variation 10786
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950625693"
variation 10790
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1445433006"
variation 10791
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1165918412"
variation 10792
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950625658"
variation 10794
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1424661283"
variation 10795
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:908782176"
variation 10796
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1228791420"
variation 10800
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950625605"
variation 10808..10809
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="t"
/replace="tt"
/db_xref="dbSNP:1344131053"
variation 10812
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:191570151"
variation 10813
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950625558"
variation 10814
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:952721192"
variation 10821
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:746372113"
variation 10822
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950625524"
variation 10827
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1023020140"
variation 10829
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950625499"
variation 10830
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1245156066"
variation 10834
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950625475"
variation 10837
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:546673452"
variation 10839
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:1950625448"
variation 10845
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1012921600"
variation 10846
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1593430788"
variation 10848
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1203423448"
variation 10861
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950625403"
variation 10862..10864
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="cc"
/replace="ccc"
/db_xref="dbSNP:1432434360"
variation 10867
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1950625366"
variation 10868
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2136892790"
variation 10869
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:959201936"
variation 10870
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1950625338"
variation 10873
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950625327"
variation 10875
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1461980175"
variation 10876
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950625297"
variation 10879
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1390404042"
variation 10886
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:940748260"
variation 10889
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950625262"
variation 10893
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1383784979"
variation 10897..10898
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="t"
/replace="tt"
/db_xref="dbSNP:1414291920"
variation 10897
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1950625242"
variation 10899
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1003369605"
variation 10900
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950625199"
variation 10903
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:902456549"
variation 10905
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:1366019933"
variation 10906
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1400631617"
variation 10909
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1452220546"
variation 10911
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:766438831"
variation 10912..10914
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="t"
/replace="tgt"
/db_xref="dbSNP:1156349086"
variation 10914..10919
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="ta"
/replace="tattta"
/db_xref="dbSNP:1950625128"
variation 10915..10926
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="atttaa"
/replace="atttaaatttaa"
/db_xref="dbSNP:1950625087"
variation 10923
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950625116"
variation 10924
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1387258188"
variation 10931
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:1452997895"
variation 10937
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950625073"
variation 10948
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:556555664"
variation 10949
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1478666759"
variation 10951
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1011005211"
variation 10957
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:893446867"
variation 10960
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1307655044"
variation 10961
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:1318710810"
variation 10966..10970
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="aatta"
/db_xref="dbSNP:1950624976"
variation 10967
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:539773802"
variation 10983..10986
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="aaaa"
/replace="aaaaaa"
/db_xref="dbSNP:1236776503"
variation 10990..10991
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="aa"
/db_xref="dbSNP:1950624944"
variation 10990
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1260288870"
variation 10992
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1324288500"
variation 10994
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:538483221"
variation 10996
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1186821585"
variation 11004
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1461173510"
variation 11005
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1178184159"
variation 11012
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1950624875"
variation 11013
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:1950624867"
variation 11014
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950624860"
variation 11017
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950624849"
variation 11019
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:932347643"
variation 11020
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1950624823"
variation 11024
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:922341581"
variation 11025
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950624797"
variation 11026
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950624779"
variation 11029
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:186860989"
variation 11031
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950624748"
variation 11032
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1593430723"
variation 11033
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1248885374"
variation 11034
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1593430717"
variation 11041
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1950624696"
variation 11048
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1593430713"
variation 11050
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:1410585713"
variation 11051
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:138234650"
variation 11054
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950624645"
variation 11056
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1178168908"
variation 11059
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="c"
/db_xref="dbSNP:1465205353"
variation 11059
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:940186812"
variation 11061
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:953399557"
variation 11064
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1593430695"
variation 11068
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:908806327"
variation 11069
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950624563"
variation 11073
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:534300505"
variation 11077
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1950624526"
variation 11084
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1389611984"
variation 11085
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950624500"
variation 11087
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="t"
/replace="tt"
/db_xref="dbSNP:541161857"
variation 11096
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:979021100"
variation 11102
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950624471"
variation 11109
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1225390783"
variation 11112
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950624328"
variation 11115
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:184356439"
variation 11116
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1035722744"
variation 11117
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950624284"
variation 11121..11125
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="ttt"
/replace="ttttt"
/db_xref="dbSNP:2136892529"
variation 11130
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1273215278"
variation 11139..11148
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="ataca"
/replace="atacaataca"
/db_xref="dbSNP:1950624219"
variation 11140
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:551774728"
variation 11142
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1225553652"
regulatory 11143..11148
/regulatory_class="polyA_signal_sequence"
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/note="hexamer: AATACA"
variation 11144
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:533152967"
variation 11145
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:982376684"
variation 11147
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950624232"
variation 11148
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950624210"
variation 11159
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950624198"
variation 11161
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1366871997"
polyA_site 11163
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
variation 11163
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:1297910724"
variation 11166
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1593430665"
variation 11168
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1009997890"
variation 11169
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950624118"
variation 11170
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1270164698"
variation 11171..11177
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="tcctgtg"
/db_xref="dbSNP:1950624086"
variation 11172
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1480496159"
variation 11178
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:895529545"
variation 11179
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="t"
/db_xref="dbSNP:1950624062"
variation 11180
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950624053"
variation 11181..11182
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="tg"
/db_xref="dbSNP:1950624023"
variation 11181
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950624040"
variation 11188
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1426576544"
variation 11191
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1035436304"
variation 11198
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950623976"
variation 11199
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1170628303"
variation 11200
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1950623955"
variation 11206
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1950623949"
variation 11210
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:757873158"
variation 11215
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1356078470"
variation 11216
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1460236380"
variation 11218..11221
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="tatt"
/replace="tattatt"
/db_xref="dbSNP:1406677966"
variation 11219
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="a"
/db_xref="dbSNP:1307377480"
variation 11220
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:111716561"
variation 11221
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:372541736"
variation 11225
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:150421734"
variation 11226
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1950623836"
variation 11227
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950623825"
variation 11228
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950623813"
ORIGIN
gcaatgtctcttgacagcggcggcggcgcagccggttccgggttcggcgcggggcggggatgtgaatcccgatggagcggcccgaggaaggcaagcagtcgccgccgccgcagccctggggacggctcctgcgtctgggcgcggaggagggcgagccgcacgtcctcctgaggaagcgggagtggaccatcgggcggagacgaggttgcgacctttccttccccagcaataaactggtctctggagatcactgtagaattgtagtggatgaaaaatcaggtcaggtgacactggaagataccagcaccagtggaacagtgattaacaagctgaaggttgttaagaagcagacatgccctttacagactggggatgtcatctacttggtgtacaggaagaatgaaccggaacacaacgtggcatacctctatgaatctttaagtgaaaagcaaggcatgacacaagaatcctttgatacctcaggtgcaggtgcagggcgaggggccgatccccgggtccctccgtcgtcgcccgccactcaggtgtgctttgaggaaccacagccatcaacatcgacgtcagacctcttccccacagcctcggcctcttccacggagccttctcctgcagggcgagagcgttcctccagttgtgggtctgggggtggtggcatctcccctaaaggaagtggtccctctgtggcaagtgatgaagtctccagctttgcctcagctctcccagacagaaagactgcgtccttttcgtcgttggaaccccaggatcaggaggatttggagcccgtgaagaagaaaatgagaggagatggggaccttgacctgaacgggcagttgttggtcgcacaaccgcgtagaaatgcccaaaccgtccacgaggacgtcagagcagcggctgggaagccagacaagatggaggagacgctgacatgcatcatctgccaggacctgctgcacgactgcgtgagtttgcagccctgcatgcacacgttctgcgcggcttgctactcgggctggatggagcgctcgtccctgtgtcctacctgccgctgtcccgtggagcggatctgtaaaaaccacatcctcaacaacctcgtggaagcatacctcatccagcatccagacaagagtcgcagtgaagaagatgtgcaaagtatggatgccagaaataaaatcactcaagacatgctgcagcccaaagtcaggcggtctttttctgatgaagaagggagttcagaggacctgctggagctgtcagacgttgacagtgagtcctcagacattagccagccatacgtcgtgtgccggcagtgtcctgagtacagaaggcaggcggcgcagcctccccactgcccagcacccgagggcgagccaggagccccacaggccctgggggatgcaccctccacgtccgtcagcctgacgacagcagtccaggattacgtgtgccctctgcaaggaagccacgccctgtgcacctgctgcttccagcccatgcccgaccggagagcggagcgcgagcaggacccgcgtgtcgcccctcagcagtgtgcggtctgcctgcagcctttctgccacctgtactggggctgcacccggaccggctgctacggctgcctggccccgttttgtgagctcaacctgggtgacaagtgtctggacggcgtgctgaacaacaacagctacgagtcagacatcctgaagaattacctggcaaccagaggtttgacatggaaaaacatgttgaccgagagcctcgtggctctccagcggggagtgtttctgctgtctgattacagagtcacgggagacaccgttctgtgttactgctgtggcctgcgcagcttccgtgagctgacctatcagtatcggcagaacattcctgcttccgagttgccagtggccgtaacatcccgtcctgactgctactggggccgtaactgccgcactcaggtgaaagctcaccacgccatgaaattcaatcatatctgtgaacagacaaggttcaaaaactaagcatccagaggccctgagcagctttcagcactggaggtgaagagagcgtgtttttaaaatacagagacaagcacgtcaaggtgttttcacagccccctgagggaagggacgcagggtctccgacaggtgctctggggtgactcttctgtggagctttaccctctgagtgagaccctccccagagccccgggggccgcagcccgccctcctggtgagcgctgggcagggctcgtggtggcatcagcagcagagacgaagcctttctgtaacatgcggccgtcccgccgagaggggcagttttgctcttttgtacattttccgaaactacagttaaagcagaagtctgtttttaggaaaagtttcaagggagaagggcaagtttatcaaaaacattgtttcaggagaagggagcataagtttacagcctacaggacgtacacaatatcctgctgctgggaaaaccacagcattttatctattttttattttaataggtttggtgcttatcttctaataagatttaaatgtcacaaactgtagcacaaataatataatttataatttacaaattgactaaaattgggtatagtatggtatttgaaagaataagcatatgcttctgtttattaaaaaaagaaaccttccaatgtccaaaactgctaaccctcgacgtggccgccaagttagtcgctccttgctaaccggtgagtgaccgcggccccgagcctggggctggacgcaggtcccaggacatgctgctcccttgtgtgagtgaccgcggccccgagcctggggctggacgcaggtcccaggacgtgctgctcccttgtgtgagtgaccacggccccaagcccagggctggaggcaggtcccaggacgcgccgctccctcatgctgcccgggcccttcctccaagaccctacagagcctgaggggcaccttggcttccgcctgtgctagctttgccatgtcatctggaataatacttgaaattttgatttttggaaaaaaaagttttttatcttttgttgaaatcacctgttatccttgtttgtaaactgataacttttttgcttcttctcaggaatacagttttcaactgttgtcttgctcttgatagaaactgagaagcagcaatctgtatttgtggaggaaagtcctctcttttgcatattctaataaatgagccgcgtttgctcctccgctctcgtgttgggctcgtgtctggggctgcctcacttccccatgcgagggaggcaggccccatgcagagtgagctccgagtgcctcactgctagtgatggtcactctgtcacctgctgtccctcagtgactcctgtgaaacctgctcaggtctcttcattctgccaatgctgggaagccacaacctgttcatccagtgtggaggctttgtcttcagctgagcaccagaagaagccacaatgcagagaccctgagtttgtgcaagggtggggctgagaggggaggtcccgtgttagtgcaggggtgaggccgggaggggaggtcccgagtttgtgtaggggcgaggctgagcagggaggttctgagttagtgcaggggcgaggctgagcagggaggtcccgagttagtgcaggggcgaggctaagggggaggtcccaagtttgtgcaggggtgaggctgagcagggaggtcccaagttagtgcaggggcgaggctgagaggggagatcccgagtttgtgcaggggcgaggctgagaggggaggtccctagttagtgcaggggtgaggccgagaagggaggtcccaagtttgtgcatggatgaagccaaaaggggagtttgcacgtttgtgcaggggtgaggccaagaagggaagtcttgagttggtgcaggggtgagggagaggggaggtcctgagtttgtgcagaggcgaggctgagaggggaggtccctaagtgcaggggtgaggccgagaggggaggttgcaaatttgtgcaggggtgaggccaagaggggaggtcctgagttagtgcgggggtgaggccgagaggggaggtcctgagtttgtgcagaggcgaggctgagaggggaggtccttagtgcaggggtgaggctgagagggggaggtcccaagtttgtgcaggggtgaggccgaggggaggttgcaagtttgtgcaggggtgaggccaagaggggaggtcctgagttagtgcgggggtgaggccgagaggggagttcctgagtttgtgcagaggcgaggctgagaggggaggttgccagtttgtgcaggtgcgaggctgagaggggaggctggcattcgccaatgaagtgggctggggctaccctgcgtctgtgtcttagagagatcggttgatactcactcttccccttcccatctccaaaaagtagaaacaagaacacttgccctgtagaggatgctggtctttcctcaggaccagctgcacctgtccaggaagggcaggcagctcagagagcctctgggctccaggtgtcctagggactcactcctgcttccttagtccttcagagaagtccaactcctggcccactgtgaagaggatttctacctggagcagtcggaacagcttgggtttggctgtgatgtgagggaggaggccttgggagcagggcagttatcctcccagcgtggtaaggagccgtgttttatggaggcagggagatcagggcagttactcctcgggtgtggtaaggagctgtgttttatggaagcaggtggccgtgaactcattccgtcttttcatgagcttctgtacttcctcgtcctcaagacccagccatcccacccagcaaaactgaccggctgtggtggttttggagccctgctctccttgtggggtggctgcgtgggtcgtccacaggctttctggaggacagcctggtgctgctgcagatcccactgcttcttcctggctccttggcccagccttgggacaaacccagggcaggg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acctcccacagtgctgggattccaggcgtaagccgccacgcccagcaactccgtttcttacttgttggctcacattctcctgagaagtcctccctcaaccatcggcctgaaatagcagcgagcctccccagggttgcctctgccttttcttgactctttctgtcaccttctatgcttgttgtctggtccccactagaatataccttctgtaagagcagggatttgggacagtgcctagaatagtacttgcagacagtaggctacgataaatatgaatgacggccccatgcagatggtagcccctctcgctcgaacgcttcacccagttttattttcttttcatcagttaccgccctctgaaggtatccacacacaaacatgaaactggaccaaagcagggaccccccgcacgcagaatagtgctgggctcgcgtaaggcacctcagtgggtccatcagctgatgcatggacagacaaaatgggtgtatccagacactggagtatcgtgcagcgaggaaacgtgctgagtgtggatggaccttaaacacaccatgcaagtgaaaaggcgtcacagaaggccacatacgatatgatcccatttctatgaaatgtccagaagaggcacattcataaagacagaaggtgactgagtggttgtcgggctgggtggaggggatagggagtgaatgcaagaaggatccttctgaggtaacggaagtatccggaaactgggttggagtgatgggtgcacagctctgcacatttactacagtcgctgaactgcacacacaacacgggtatattttattgcatagaaattgtattaaagctgttaagaattttacttagattagcatttttcccacactgtgccatcaacttagtatatgattagattcattgtttctaactgtatttaaatttaatgtttgtcacattttgcttgctaaatttttaaaattttaaattactgtgggtacataaaaggtgtatatatttatggagtaccttgatattttaatacagacatacaatgtataatgatcaactcccagtaactggggtatccatcacctcaagcctgtatcatttctttgttaggaacattccagttccactctttttgttatttaaaaatatacaatacattattattaactatattcaccctcctgtgctatggaatactagatcttatgctaattaaatgttttccctatttctccca
//
by
@meso_cacase at
DBCLS
This page is licensed under a
Creative Commons Attribution 4.0 International License (CC BY 4.0).
If you use GGRNA in your work, please cite:
Naito Y, Bono H. (2012)
GGRNA: an ultrafast, transcript-oriented search engine for genes and transcripts.
Nucleic Acids Res., 40, W592-W596.
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