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Previous release (v1)
2024-04-20 22:22:07, GGRNA.v2 : RefSeq release 222 (Jan, 2024)
LOCUS NM_001161345 3288 bp mRNA linear PRI 17-APR-2023
DEFINITION Homo sapiens checkpoint with forkhead and ring finger domains
(CHFR), transcript variant 2, mRNA.
ACCESSION NM_001161345
VERSION NM_001161345.1
KEYWORDS RefSeq.
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 3288)
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 3288)
AUTHORS Hagiwara T, Sugimoto K, Momose H, Irie T, Honjo K, Okazawa YU,
Kawai M, Kawano S, Munakata S, Takahashi M, Kojima Y, Serizawa N,
Nagahara A, Hoffman RM, Brock MV 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 3288)
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 3288)
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 3288)
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 3288)
AUTHORS Sanbhnani S and Yeong FM.
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 3288)
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 3288)
AUTHORS Chaturvedi P, Sudakin V, Bobiak ML, Fisher PW, Mattern MR,
Jablonski SA, Hurle MR, Zhu Y, Yen TJ and Zhou BB.
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 3288)
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 3288)
AUTHORS Scolnick DM and Halazonetis TD.
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 BP313700.1, AK304333.1,
AK027687.1, AC127070.10 and BC012072.1.
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: This RefSeq record was created from transcript and
genomic sequence data to make the sequence consistent with the
reference genome assembly. The genomic coordinates used for the
transcript record were based on transcript 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 :: AK304333.1 [ECO:0000332]
RNAseq introns :: mixed sample support SAMEA1965299,
SAMEA1966682 [ECO:0006172]
##Evidence-Data-END##
COMPLETENESS: complete on the 3' end.
PRIMARY REFSEQ_SPAN PRIMARY_IDENTIFIER PRIMARY_SPAN COMP
1-13 BP313700.1 1-13
14-968 AK304333.1 1-955
969-969 AK027687.1 927-927
970-1785 AK304333.1 957-1772
1786-1877 AK027687.1 1747-1838
1878-2146 AK304333.1 1865-2133
2147-2931 AC127070.10 108335-109119
2932-3288 BC012072.1 2825-3181
FEATURES Location/Qualifiers
source 1..3288
/organism="Homo sapiens"
/mol_type="mRNA"
/db_xref="taxon:9606"
/chromosome="12"
/map="12q24.33"
gene 1..3288
/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..72
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/inference="alignment:Splign:2.1.0"
variation 1
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:1361815684"
variation 3
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1951934322"
variation 4
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:1003781663"
variation 6
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:1951934250"
variation 7
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1287541768"
variation 11
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:553012411"
variation 12
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:905468008"
variation 13
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1951934082"
variation 14
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1951934047"
variation 16
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:534357480"
variation 17
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:570446374"
variation 18
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:896280970"
variation 21
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1951933832"
variation 23
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1452969814"
variation 24
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1468914426"
variation 25
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1951933697"
variation 27
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1951933660"
variation 28..31
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="cagc"
/replace="cagcagc"
/db_xref="dbSNP:1951933544"
variation 29
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1403273314"
variation 30..41
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="gcggcggcg"
/replace="gcggcggcggcg"
/replace="gcggcggcggcggcg"
/db_xref="dbSNP:1462255454"
variation 30
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1052274666"
variation 31
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2137089264"
variation 32
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1023737356"
variation 33
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1951933454"
variation 34
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2137089243"
variation 35
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1177915172"
variation 36
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1305328622"
variation 37
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1043377910"
variation 38
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:942391667"
variation 39
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:910903529"
variation 40..42
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="cgc"
/replace="cgccgc"
/db_xref="dbSNP:1951933091"
variation 40
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:986491943"
variation 41
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1593552393"
variation 42
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1951933065"
variation 43
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:867733545"
variation 44
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:866582582"
variation 45
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1184602056"
variation 46
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1457982394"
variation 47
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1180202481"
variation 48
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1951932815"
variation 49
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:955129324"
variation 50
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1418375663"
variation 52
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:918721775"
variation 53
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1379340094"
variation 54
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:558080896"
variation 55
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1401227842"
variation 58
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1203285887"
variation 59
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1373084089"
variation 60
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1460094658"
variation 61
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1951932409"
variation 62
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:972910573"
variation 63
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:962990830"
variation 64
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1951932291"
variation 68
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1210883392"
variation 69
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1261984726"
variation 70
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1951932164"
variation 71
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1318118652"
variation 72
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1307468722"
exon 73..217
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/inference="alignment:Splign:2.1.0"
variation 75
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1951922592"
misc_feature 76..78
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/note="upstream in-frame stop codon"
variation 76
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1951922549"
variation 81..83
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="cc"
/replace="ccc"
/db_xref="dbSNP:1000300479"
variation 81
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:756050840"
variation 82
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1200689283"
variation 83
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:745782659"
variation 84
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1951922329"
CDS 85..2076
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/EC_number="2.3.2.27"
/note="isoform 2 is encoded by transcript variant 2; 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 2"
/protein_id="NP_001154817.1"
/db_xref="GeneID:55743"
/db_xref="HGNC:HGNC:20455"
/db_xref="MIM:605209"
/translation="
MERPEEGKQSPPPQPWGRLLRLGAEEGEPHVLLRKREWTIGRRRGCDLSFPSNKLVSGDHCRIVVDEKSGQVTLEDTSTSGTVINKLKVVKKQTCPLQTGDVIYLVYRKNEPEHNVAYLYESLSEKQGMTQESFEANKENVFHGTKDTSGAGAGRGADPRVPPSSPATQVCFEEPQPSTSTSDLFPTASASSTEPSPAGRERSSSCGSGGGGISPKGSGPSVASDEVSSFASALPDRKTASFSSLEPQDQEDLEPVKKKMRGDGDLDLNGQLLVAQPRRNAQTVHEDVRAAAGKPDKMEETLTCIICQDLLHDCVSLQPCMHTFCAACYSGWMERSSLCPTCRCPVERICKNHILNNLVEAYLIQHPDKSRSEEDVQSMDARNKITQDMLQPKVRRSFSDEEGSSEDLLELSDVDSESSDISQPYVVCRQCPEYRRQAAQPPHCPAPEGEPGAPQALGDAPSTSVSLTTVQDYVCPLQGSHALCTCCFQPMPDRRAEREQDPRVAPQQCAVCLQPFCHLYWGCTRTGCYGCLAPFCELNLGDKCLDGVLNNNSYESDILKNYLATRGLTWKNMLTESLVALQRGVFLLSDYRVTGDTVLCYCCGLRSFRELTYQYRQNIPASELPVAVTSRPDCYWGRNCRTQVKAHHAMKFNHICEQTRFKN"
misc_feature 85..147
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/note="propagated from UniProtKB/Swiss-Prot (Q96EP1.2);
Region: Disordered. /evidence=ECO:0000256|SAM:MobiDB-lite"
misc_feature 127..456
/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(127..150,202..204,226..228,232..234,241..243,
247..252,262..267,298..318,322..360,367..378,385..408,
430..456)
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/note="homodimer interface [polypeptide binding]; other
site"
/db_xref="CDD:438724"
misc_feature order(205..213,253..258,262..264,316..327)
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/note="putative phosphopeptide binding site [polypeptide
binding]; other site"
/db_xref="CDD:438724"
misc_feature 508..885
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/note="propagated from UniProtKB/Swiss-Prot (Q96EP1.2);
Region: Disordered. /evidence=ECO:0000256|SAM:MobiDB-lite"
misc_feature 814..816
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/note="Phosphoserine.
/evidence=ECO:0007744|PubMed:23186163; propagated from
UniProtKB/Swiss-Prot (Q96EP1.2); phosphorylation site"
misc_feature 976..>1587
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/note="DNA repair protein rad18; Region: rad18; TIGR00599"
/db_xref="CDD:273165"
misc_feature 982..1143
/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 1240..1242
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/note="Phosphothreonine.
/evidence=ECO:0000250|UniProtKB:Q810L3; propagated from
UniProtKB/Swiss-Prot (Q96EP1.2); phosphorylation site"
misc_feature 1246..1335
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/note="propagated from UniProtKB/Swiss-Prot (Q96EP1.2);
Region: Disordered. /evidence=ECO:0000256|SAM:MobiDB-lite"
misc_feature 1399..1467
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/note="propagated from UniProtKB/Swiss-Prot (Q96EP1.2);
Region: Disordered. /evidence=ECO:0000256|SAM:MobiDB-lite"
misc_feature 1486..1941
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/note="Cysteine rich domain with multizinc binding
regions; Region: zf-CRD; pfam17979"
/db_xref="CDD:436187"
misc_feature 1975..2046
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/note="Zinc-finger (CX5CX6HX5H) motif; Region: zf-CCHH;
pfam10283"
/db_xref="CDD:431197"
variation 85
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1951922287"
variation 87
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1323042743"
variation 89
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:780919643"
variation 92
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:757065782"
variation 93
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:879451433"
variation 94
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1252988651"
variation 100
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1285867152"
variation 104
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1453369842"
variation 107
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1381686714"
variation 109
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1334460653"
variation 113..124
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="cgccgccgc"
/replace="cgccgccgccgc"
/replace="cgccgccgccgccgc"
/db_xref="dbSNP:765917829"
variation 113
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:752932212"
variation 115
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:372093401"
variation 117
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1566211828"
variation 118
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1459172597"
variation 121
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1022133046"
variation 122
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1407689006"
variation 123
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1415407421"
variation 124
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1951921415"
variation 126
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1184750358"
variation 127
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1444571399"
variation 129
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:547086677"
variation 131..134
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="ggg"
/replace="gggg"
/db_xref="dbSNP:1180924768"
variation 131
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1951921231"
variation 136
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1481059648"
variation 137
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1951921084"
variation 138
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1593551043"
variation 139
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1951920986"
variation 141
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1327949016"
variation 142
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1250940821"
variation 143
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:2137086568"
variation 145
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1951920825"
variation 146
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1202757955"
variation 148
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1323574369"
variation 151
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1292594475"
variation 153
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1246548917"
variation 155
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1951920619"
variation 156
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:753867941"
variation 157
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1312590714"
variation 159
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1448675201"
variation 161
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1373843772"
variation 165
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1297235638"
variation 169
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:766461060"
variation 170
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1242357676"
variation 171
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:889736424"
variation 172
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1050716303"
variation 174
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1163686245"
variation 175
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1424534907"
variation 177
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:761126986"
variation 178
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:896897715"
variation 180
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1161017404"
variation 181
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:558346895"
variation 183
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1291046887"
variation 186
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:994965729"
variation 189
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1250327307"
variation 190
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1951919733"
variation 191
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1037164725"
variation 192
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1175632960"
variation 195
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:2137086327"
variation 198
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1489596045"
variation 201
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1269637112"
variation 202
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1329871429"
variation 204
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="c"
/db_xref="dbSNP:2043630516"
variation 205
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1220935343"
variation 207
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1360131934"
variation 208
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:941122476"
variation 212
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1951919358"
variation 214
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1221878184"
variation 215
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1951919241"
exon 218..317
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/inference="alignment:Splign:2.1.0"
variation 219..220
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="t"
/replace="tt"
/db_xref="dbSNP:1566203316"
variation 221
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:762757910"
variation 222
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:775199616"
variation 223
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1016169013"
variation 226
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:370348872"
variation 229
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1184762410"
variation 232
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:776467669"
variation 234..237
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="ccc"
/replace="cccc"
/db_xref="dbSNP:2137047496"
variation 234
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1371415158"
variation 235
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:765839818"
variation 236
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:770855105"
variation 238
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:146088609"
variation 239
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1951658569"
variation 239
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="gg"
/db_xref="dbSNP:1951658615"
variation 241
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:77052806"
variation 243
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1951658472"
variation 244
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:540426488"
variation 249
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:771849929"
variation 250
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1951658327"
variation 252
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1951658293"
variation 253
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1951658241"
variation 254
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1325393287"
variation 257
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:573017098"
variation 258
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:780255609"
variation 259
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:956973617"
variation 262
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:756177652"
variation 263
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:1336502857"
variation 264
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1468386635"
variation 272
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:750466757"
variation 274
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:781107351"
variation 275
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:142824452"
variation 277
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1372280960"
variation 278
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:752104453"
variation 283
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1190933998"
variation 289..299
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="tcaggt"
/replace="tcaggtcaggt"
/db_xref="dbSNP:1951657458"
variation 291
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1446377947"
variation 292
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:764607751"
variation 296
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:763356188"
variation 302
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1436266778"
variation 303
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:115711908"
variation 304
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1252203966"
variation 306
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1951657255"
variation 309
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1390531305"
variation 314
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1196075617"
variation 315
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:764905392"
variation 317
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:996565819"
exon 318..427
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/inference="alignment:Splign:2.1.0"
variation 320
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1405603798"
variation 321
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:200283117"
variation 324
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1951510439"
variation 326
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1951510403"
variation 330
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:138320999"
variation 333
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1262248032"
variation 341
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1403538188"
variation 342
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1593510822"
variation 349..354
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="gtt"
/replace="gttgtt"
/db_xref="dbSNP:749471534"
variation 351
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1026698840"
variation 356
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1951510106"
variation 358
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:753427887"
variation 360
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1409273260"
variation 361
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:765931951"
variation 362
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:145622325"
variation 363
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:896801495"
variation 366
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1951509886"
variation 370
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1220821081"
variation 371
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1951509767"
variation 375
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1951509715"
variation 377
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:773164146"
variation 379
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:1285340068"
variation 388
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1593510705"
variation 391
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1204882792"
variation 395
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:1349041006"
variation 397
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:767392115"
variation 399
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:761633567"
variation 400
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:774239471"
variation 405
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:768330210"
variation 407
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1951509269"
variation 413
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1281470229"
variation 415
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1036686943"
variation 417
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1277101257"
variation 419
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:377703818"
variation 420
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:771143796"
variation 424
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:201058448"
variation 425
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:778449705"
variation 426
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1951508921"
variation 427
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:758996497"
exon 428..487
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/inference="alignment:Splign:2.1.0"
variation 429
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:368692761"
variation 430
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:765096474"
variation 433
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1300704622"
variation 435
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:761045629"
variation 436
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1402185439"
variation 439
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:773555344"
variation 442
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1951471364"
variation 443
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:772208422"
variation 450..452
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="ttt"
/replace="tttt"
/db_xref="dbSNP:2137020043"
variation 451
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1428337510"
variation 454
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1387598301"
variation 455
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1951471200"
variation 462
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1164831443"
variation 466
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:202105666"
variation 467
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:769092725"
variation 469
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1415955003"
variation 472
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1312795252"
variation 474
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:374502930"
variation 475
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:761297928"
variation 476
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1481092256"
variation 478
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:780460479"
variation 480
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:773617187"
variation 483
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1443614623"
variation 486
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1951470668"
exon 488..703
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/inference="alignment:Splign:2.1.0"
variation 490
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:997424313"
variation 494
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1287311542"
variation 495
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:141763844"
variation 500
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:767585723"
variation 501
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1277771516"
variation 502
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1283386653"
variation 503
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1404832547"
variation 504..508
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="tgt"
/replace="tgtgt"
/db_xref="dbSNP:1951443370"
variation 507
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1038860837"
variation 510
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2137015845"
variation 511
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1366157844"
variation 512
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1951443217"
variation 513
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:547902011"
variation 518
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1951443114"
variation 521
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:1454615091"
variation 524
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:1415698891"
variation 527..530
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="cctc"
/db_xref="dbSNP:1951442868"
variation 527
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1951442959"
variation 529
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:1951442927"
variation 530..545
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="caggtgcagg"
/replace="caggtgcaggtgcagg"
/replace="caggtgcaggtgcaggtgcagg"
/db_xref="dbSNP:1566196191"
variation 531
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1951442837"
variation 534
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1345035376"
variation 538
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:529705996"
variation 539
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:968187911"
variation 540
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1053846225"
variation 545..546
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="tgcagt"
/db_xref="dbSNP:1951442404"
variation 545
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1430015478"
variation 546
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1566196184"
variation 548
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:761341813"
variation 550..553
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="gggg"
/replace="ggggg"
/db_xref="dbSNP:1431549533"
variation 555
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1265155365"
variation 556
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:768775618"
variation 559
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:565366267"
variation 560
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1267263973"
variation 561
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:547367271"
variation 562
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:746187833"
variation 563
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:780923793"
variation 564
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1951441836"
variation 565
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1951441794"
variation 569
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1231852845"
variation 570
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1309985498"
variation 572
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1298364440"
variation 573
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1951441603"
variation 574
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1951441554"
variation 575
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1030329804"
variation 576
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:199790262"
variation 577
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1318983295"
variation 578
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:371470066"
variation 579
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:777219646"
variation 581
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1176037831"
variation 582
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1422710949"
variation 583
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:998173223"
variation 584
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1951441033"
variation 586
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1359228046"
variation 587
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:757969077"
variation 589
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:748110156"
variation 590
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1951440849"
variation 591
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:991093892"
variation 592
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:775208965"
variation 594
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1186481589"
variation 596
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1462519990"
variation 597
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1951440598"
variation 608
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1951440531"
variation 609
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1212965676"
variation 610
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1243354590"
variation 611
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:756710137"
variation 613
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1951440329"
variation 614
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1951440283"
variation 617
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1951440243"
variation 618
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1951440193"
variation 620
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:959491929"
variation 621
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:753235007"
variation 623
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:778929950"
variation 624
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:909400005"
variation 626
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1252563891"
variation 627
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:754853631"
variation 634
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1342113004"
variation 639
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1296093228"
variation 640
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:368788828"
variation 643
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1398898916"
variation 644
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1951439655"
variation 647
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:984493040"
variation 650
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1048846757"
variation 651
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:528825047"
variation 652
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:564810555"
variation 653
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1382340206"
variation 657
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:751789347"
variation 658
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1298843354"
variation 659
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:546136386"
variation 660
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1430290279"
variation 662
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:541715629"
variation 663
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:75391939"
variation 664
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1593503337"
variation 665
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1166700448"
variation 666
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1951438999"
variation 669
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1446218228"
variation 671..675
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="ct"
/replace="ctcct"
/db_xref="dbSNP:1593503293"
variation 673
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1385634222"
variation 676
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1951438819"
variation 678
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:965751134"
variation 681
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:563840755"
variation 682
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:745321936"
variation 683
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:776005190"
variation 688
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1042155534"
variation 689
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:765687815"
variation 694
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:1460603946"
variation 695
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1951438339"
variation 697
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1381533831"
variation 701
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1225450271"
exon 704..871
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/inference="alignment:Splign:2.1.0"
variation 707
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1038150337"
variation 709
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:370517411"
variation 710
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1951211639"
variation 712
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1438318944"
variation 713
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:777186106"
variation 715..716
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="gg"
/db_xref="dbSNP:1189456093"
variation 715
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:766667278"
variation 718
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:761034338"
variation 719
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1593482765"
variation 721
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:138637226"
variation 723
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1951211154"
variation 724
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1387477118"
variation 727
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:34220055"
variation 728
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:761525824"
variation 729
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2136982888"
variation 734
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1951210868"
variation 737
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:774070010"
variation 738
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:1419993206"
variation 739
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1951210693"
variation 740
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:201192149"
variation 741
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:989203291"
variation 743
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1951210512"
variation 747
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:796201985"
variation 748
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1163339779"
variation 756
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:749192848"
variation 760
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:374107669"
variation 762
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:769505625"
variation 767
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:780945230"
variation 771
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1951210091"
variation 780
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1951210040"
variation 784
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:35206714"
variation 786
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1951209926"
variation 787
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1366834805"
variation 789
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1038008124"
variation 791
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:560433355"
variation 793..799
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="aga"
/replace="agaaaga"
/db_xref="dbSNP:1951209560"
variation 796
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:201727566"
variation 800
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:2136982730"
variation 801
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:758662673"
variation 802
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:533118486"
variation 803
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:150995074"
variation 804
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:755027328"
variation 805..809
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="t"
/replace="tcctt"
/db_xref="dbSNP:2136982677"
variation 807
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:908433616"
variation 810
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:200213031"
variation 812
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:754307363"
variation 813
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:145246258"
variation 815
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:141183005"
variation 816
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:767988129"
variation 817..818
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="t"
/replace="tt"
/db_xref="dbSNP:766718829"
variation 819
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1566189184"
variation 820
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1423637297"
variation 823..826
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="ccc"
/replace="cccc"
/db_xref="dbSNP:762524769"
variation 823
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:751592981"
variation 825
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1951208832"
variation 827
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:373754363"
variation 828
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:761615752"
variation 829
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:147803776"
variation 831
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1566189143"
variation 833
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1951208615"
variation 837
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:774088595"
variation 838
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1472958431"
variation 846
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:768052255"
variation 847..849
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="cc"
/replace="ccc"
/db_xref="dbSNP:2136982524"
variation 848
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:762481129"
variation 849
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1025589682"
variation 850
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:775309126"
variation 852
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:764279540"
variation 853
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1951208249"
variation 854
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1463671908"
variation 856
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:974854406"
variation 859
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:1221100387"
variation 860
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1951208117"
variation 861
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:1238379063"
variation 862
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1951208036"
variation 863
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1566189061"
variation 868
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:745763828"
exon 872..1031
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/inference="alignment:Splign:2.1.0"
variation 872
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1951157533"
variation 873
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:756088633"
variation 876
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1951157390"
variation 877
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:563202190"
variation 880
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2136974267"
variation 881
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1360404336"
variation 884
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1951157150"
variation 885
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:781748631"
variation 888
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:757715316"
variation 890
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:752016583"
variation 891
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:377318460"
variation 892
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:115096950"
variation 893
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1593477819"
variation 894
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1393923793"
variation 895..896
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="t"
/db_xref="dbSNP:776753889"
variation 896
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:1311480210"
variation 897
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:758139441"
variation 898
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:973250523"
variation 900
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1021390710"
variation 904
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:752281100"
variation 906
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:115431373"
variation 907
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:148618944"
variation 909
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:369526598"
variation 912
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:769878915"
variation 913
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:540759128"
variation 914
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:760584451"
variation 915
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:773102049"
variation 916
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:749537035"
variation 917
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:375174098"
variation 919
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:770024903"
variation 922
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1951155348"
variation 925
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:188170704"
variation 926
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:745889598"
variation 927
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1951155139"
variation 928
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:781395404"
variation 930
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:757876886"
variation 931
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1593477690"
variation 932
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1951154950"
variation 933
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:747517165"
variation 934
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:199761208"
variation 937
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1951154859"
variation 939
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1380131918"
variation 940
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:144838296"
variation 942
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1449844658"
variation 944
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1000960906"
variation 945
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:371434249"
variation 946
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:764757412"
variation 947
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="t"
/db_xref="dbSNP:768680290"
variation 947
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1464052810"
variation 949
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:754506935"
variation 950
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:149862277"
variation 953
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2136973920"
variation 954
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:765845584"
variation 956
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1277312621"
variation 957
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:746414469"
variation 958
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1341883561"
variation 959
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:2136973888"
variation 960
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1295926976"
variation 962
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1306779303"
variation 964
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1593477559"
variation 965
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1375950961"
variation 968
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2136973857"
variation 969
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:35011845"
variation 970
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1341253353"
variation 972
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1951153923"
variation 975
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1312306793"
variation 976
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:767348322"
variation 978
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1352413194"
variation 981
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2136973793"
variation 984
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:2136973786"
variation 986
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:761474515"
variation 987
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:775799321"
variation 988
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2136973760"
variation 990
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1951153687"
variation 991
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1951153632"
variation 993
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1369689338"
variation 995
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2136973741"
variation 997
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1951153534"
variation 999
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:770185579"
variation 1000
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1252007101"
variation 1002
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:12315353"
variation 1005
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:146107503"
variation 1011
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1368629651"
variation 1014
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1186411942"
variation 1015
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1951153233"
variation 1016
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:759798633"
variation 1017
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:2136973671"
variation 1018
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1951153155"
variation 1020
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1253421391"
variation 1021
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1951153058"
variation 1026
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:776915637"
variation 1027
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:771123706"
variation 1029
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1469130916"
exon 1032..1186
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/inference="alignment:Splign:2.1.0"
variation 1032
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:560066373"
variation 1036
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1213141444"
variation 1040
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:780721649"
variation 1041
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:565644778"
variation 1045
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:987211916"
variation 1048
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1566185781"
variation 1049
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1174814592"
variation 1050
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1478670195"
variation 1052
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:751498855"
variation 1053
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:142975525"
variation 1056
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1466544467"
variation 1059
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:138280939"
variation 1060
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:754144763"
variation 1061
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:921635691"
variation 1062
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:766660009"
variation 1063
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:760933260"
variation 1064
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1221124973"
variation 1070
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:368405665"
variation 1071
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:767634272"
variation 1073
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:762287710"
variation 1074
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1367099211"
variation 1076
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:774770261"
variation 1077
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1951109519"
variation 1081
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1433978124"
variation 1083
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:553735979"
variation 1084..1086
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="gag"
/replace="gagag"
/db_xref="dbSNP:1566185670"
variation 1085
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:968563777"
variation 1087
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:749601873"
variation 1088
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:775805064"
variation 1091
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1402056016"
variation 1092
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:769371058"
variation 1093
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1593473549"
variation 1095
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:745529097"
variation 1096..1097
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="ct"
/db_xref="dbSNP:1951108714"
variation 1099
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1951108652"
variation 1101
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:780623191"
variation 1105
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:535313174"
variation 1106
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:756736276"
variation 1108
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1474574138"
variation 1111
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:770034782"
variation 1112
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:146343801"
variation 1115
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1441931198"
variation 1117
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:571101753"
variation 1119
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:115029653"
variation 1120
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1344021759"
variation 1126
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:182092641"
variation 1127
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:756361707"
variation 1131
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1359376881"
variation 1133
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:141404869"
variation 1135
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1951107709"
variation 1136
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:767497782"
variation 1138
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1313496770"
variation 1139
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1319716667"
variation 1140
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1339366523"
variation 1142
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1951107360"
variation 1143
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1951107293"
variation 1146
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:375199215"
variation 1151
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:774858017"
variation 1152
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1951107092"
variation 1153
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1371529354"
variation 1154
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:764629991"
variation 1156
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1255988921"
variation 1158
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:191062458"
variation 1159
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:775898959"
variation 1162
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1182669640"
variation 1165
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1213131732"
variation 1166
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1241168194"
variation 1169
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1593473382"
variation 1170
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:148311652"
variation 1173
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:143181439"
variation 1174
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1241159400"
variation 1175
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1593473335"
variation 1176
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:770380694"
variation 1180
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:746470663"
variation 1181
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:370386571"
variation 1182
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2136966487"
variation 1184
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1951106171"
exon 1187..1349
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/inference="alignment:Splign:2.1.0"
variation 1188
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1227736511"
variation 1189..1190
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="aa"
/db_xref="dbSNP:777961507"
variation 1195
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1210874026"
variation 1197
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:928539042"
variation 1201..1208
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="gaaga"
/replace="gaagaaga"
/db_xref="dbSNP:1951075030"
variation 1201
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1951075098"
variation 1203
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1566184554"
variation 1210
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:879123151"
variation 1212
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1229649968"
variation 1214
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:777930523"
variation 1215
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1566184534"
variation 1217
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1293723698"
variation 1219
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:377225060"
variation 1223
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:748309050"
variation 1224
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:778828908"
variation 1225
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1434082116"
variation 1226
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:200764395"
variation 1227
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:369063253"
variation 1228
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:1026572995"
variation 1229
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:766865645"
variation 1230
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:2062163"
variation 1238
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1047280041"
variation 1239
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:750119581"
variation 1241
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:760238279"
variation 1243
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:761337268"
variation 1249
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:150467142"
variation 1257
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:763498728"
variation 1261
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1951074170"
variation 1266
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:930183182"
variation 1267
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1322357484"
variation 1268
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:762961678"
variation 1269
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:879252133"
variation 1270
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:920205326"
variation 1271
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:201828860"
variation 1273
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1593470536"
variation 1274
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:769607729"
variation 1275
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:745615761"
variation 1278
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:776390811"
variation 1282
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:974463026"
variation 1285..1291
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="gaag"
/replace="gaagaag"
/db_xref="dbSNP:1434190222"
variation 1292
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:772321674"
variation 1295
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1315657949"
variation 1298
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="cc"
/db_xref="dbSNP:1951073572"
variation 1298
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1413044699"
variation 1302
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1353432969"
variation 1306
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1951073448"
variation 1309
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1309789349"
variation 1314
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:748314312"
variation 1320
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1283784330"
variation 1321
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1951073286"
variation 1323
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1395585538"
variation 1324
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1165776578"
variation 1330
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1951073172"
variation 1332
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1951073138"
variation 1334
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:779111370"
variation 1335
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1951073053"
variation 1338
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1368718436"
variation 1340
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1951072973"
variation 1347
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:754958760"
exon 1350..1492
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/inference="alignment:Splign:2.1.0"
variation 1353
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1286314037"
variation 1354
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1020597739"
variation 1356
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:748419509"
variation 1357
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:372270460"
variation 1358
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1013270057"
variation 1359
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1438322046"
variation 1360
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:768814594"
variation 1361
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1318363216"
variation 1362
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:749373830"
variation 1363
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:150627547"
variation 1365
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:368755833"
variation 1369
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1435723841"
variation 1370
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:746360566"
variation 1371
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1191956640"
variation 1377
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1451601823"
variation 1379
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:781699438"
variation 1382
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:757496767"
variation 1386
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1192492326"
variation 1388
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950995102"
variation 1390
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1445358565"
variation 1391
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950994995"
variation 1397
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:374229656"
variation 1398
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:777240371"
variation 1399
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1303770543"
variation 1400
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:371541325"
variation 1401
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:563852229"
variation 1405
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1231849613"
variation 1406
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1950994654"
variation 1408
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1366854652"
variation 1409
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1270421677"
variation 1410
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1429332642"
variation 1412
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1176161885"
variation 1413
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:764723102"
variation 1419
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2136951422"
variation 1423
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1237028076"
variation 1425
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:759529335"
variation 1426
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:753721064"
variation 1428
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1375184437"
variation 1429
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950993996"
variation 1430
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:367968934"
variation 1431
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:374006779"
variation 1432
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:774658371"
variation 1433
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1167629443"
variation 1434
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1566181842"
variation 1435
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:924051400"
variation 1436
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1593463729"
variation 1437
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1041545091"
variation 1441
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:768798394"
variation 1443
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1239336733"
variation 1448
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950993248"
variation 1456
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950993189"
variation 1458
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1189940191"
variation 1461
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950993053"
variation 1463
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:138207644"
variation 1464
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1593463695"
variation 1465
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1256747525"
variation 1467
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1379314322"
variation 1468
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:775767314"
variation 1471
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1196421815"
variation 1472
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:769933100"
variation 1473
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:746380972"
variation 1474
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:1215461680"
variation 1476
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:781511228"
variation 1477
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:141835819"
variation 1481
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:747380214"
variation 1484
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:778169456"
variation 1486
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:1355326421"
variation 1487
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:752333209"
variation 1488
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:536396076"
exon 1493..1609
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/inference="alignment:Splign:2.1.0"
variation 1494
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:146976267"
variation 1496
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:765605647"
variation 1497
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1408464611"
variation 1501
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2136945225"
variation 1503
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:141349945"
variation 1504
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:776642806"
variation 1508
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1593459784"
variation 1509
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1306934237"
variation 1510
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:764423128"
variation 1511
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1950950185"
variation 1513
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:766469365"
variation 1515
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:761102171"
variation 1516
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2136945164"
variation 1520
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1304421220"
variation 1524
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:773703522"
variation 1525
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:772460210"
variation 1527
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:147791929"
variation 1528
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1454391193"
variation 1532
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1345653105"
variation 1533
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:116286061"
variation 1536
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:768361418"
variation 1537
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1593459724"
variation 1538
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1396714833"
variation 1539..1546
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="ctgct"
/replace="ctgctgct"
/db_xref="dbSNP:1363396811"
variation 1539
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:748952886"
variation 1540
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:763257394"
variation 1542
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1278317795"
variation 1548
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1950949058"
variation 1549
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1593459675"
variation 1550
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:779441212"
variation 1551
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:775978433"
variation 1558
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1187706335"
variation 1560
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:781224248"
variation 1561
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:757239007"
variation 1562
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1593459653"
variation 1564
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:936864653"
variation 1565
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:969442993"
variation 1568
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:751440176"
variation 1570
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1950948312"
variation 1571
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2306541"
variation 1572
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:755310429"
variation 1573
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1298012137"
variation 1575
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950947947"
variation 1576
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:754035414"
variation 1577
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:944300584"
variation 1578
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:766376169"
variation 1579
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:150920425"
variation 1582
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1015010652"
variation 1583
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:773617183"
variation 1585
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950947517"
variation 1587
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2136944907"
variation 1589
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:768065335"
variation 1590
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:142511371"
variation 1591
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:114117795"
variation 1592..1595
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="gt"
/replace="gtgt"
/db_xref="dbSNP:1950947070"
variation 1592
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:201454195"
variation 1593
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1172173801"
variation 1594
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:200436687"
variation 1596
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:920038038"
variation 1597
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:746554223"
variation 1599
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:973207321"
variation 1603
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1486915053"
variation 1605
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1346472721"
variation 1606
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1258850426"
variation 1608
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:769207559"
exon 1610..1693
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/inference="alignment:Splign:2.1.0"
variation 1612
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:372012714"
variation 1613
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:201350082"
variation 1614
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:7975454"
variation 1617
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:375656978"
variation 1623
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1335016856"
variation 1625
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:201237898"
variation 1626
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1442703181"
variation 1627
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:765505226"
variation 1628
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1324580295"
variation 1632
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950877727"
variation 1634
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950877687"
variation 1635
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950877658"
variation 1637
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1403110794"
variation 1644
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:759242088"
variation 1646..1649
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="ggg"
/replace="gggg"
/db_xref="dbSNP:1950877531"
variation 1649
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:953787024"
variation 1653
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:546055046"
variation 1654
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1593453012"
variation 1655
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:766020195"
variation 1657
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:371092913"
variation 1658
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:146156998"
variation 1659
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1454840670"
variation 1660
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:979112170"
variation 1661
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1252629926"
variation 1662
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:772089817"
variation 1663
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1448818469"
variation 1665
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1593452935"
variation 1666
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1950876982"
variation 1668
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1249069969"
variation 1670
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:767140702"
variation 1671
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:765611625"
variation 1672
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1349644861"
variation 1677
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:189987561"
variation 1678
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1236250946"
variation 1680
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:966632867"
variation 1683
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950876673"
variation 1684
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1348083185"
variation 1685
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1302248351"
variation 1686
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1433674477"
variation 1689
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1327743680"
exon 1694..1764
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/inference="alignment:Splign:2.1.0"
variation 1695
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:777921940"
variation 1700
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1950866672"
variation 1701
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:200853567"
variation 1704
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:748721756"
variation 1705
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1179840200"
variation 1707
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950866525"
variation 1708
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950866486"
variation 1710
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1471040037"
variation 1711
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:1950866384"
variation 1713
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1415191475"
variation 1715
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1233090445"
variation 1722
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:372404283"
variation 1723
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:755522022"
variation 1724
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:754297675"
variation 1725
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1323808548"
variation 1732..1741
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="aacaaca"
/replace="aacaacaaca"
/db_xref="dbSNP:1950865942"
variation 1734
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1213796881"
variation 1735
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:780565079"
variation 1736
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1288355908"
variation 1739
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1225827826"
variation 1740
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:755891788"
variation 1742
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1288380542"
variation 1746
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:749973618"
variation 1747
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950865817"
variation 1748
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:1379904886"
variation 1749
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:767082498"
variation 1753
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1950865707"
variation 1754
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:1950865670"
variation 1755
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1416698488"
variation 1759
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:761176081"
variation 1764
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1326600805"
exon 1765..1852
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/inference="alignment:Splign:2.1.0"
variation 1766
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1432073088"
variation 1767
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950847784"
variation 1770
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1422500887"
variation 1771
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:899072283"
variation 1772
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1008556440"
variation 1775
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950847611"
variation 1777
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:776466473"
variation 1779
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1950847509"
variation 1781
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:576074865"
variation 1783..1794
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="gg"
/replace="ggtttgacatgg"
/db_xref="dbSNP:1950847213"
variation 1786
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:2306537"
variation 1791
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:536151635"
variation 1792
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1281285798"
variation 1793
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1378971375"
variation 1795..1799
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="aaaaa"
/replace="aaaaaa"
/db_xref="dbSNP:1224656808"
variation 1799
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1232869629"
variation 1801
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:200187965"
variation 1807
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:2136929281"
variation 1809
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:749821203"
variation 1810
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:780655269"
variation 1816
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:770399858"
variation 1818
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:899313894"
variation 1819
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2306536"
variation 1822
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1485801990"
variation 1823
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:781614371"
variation 1824
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:756917083"
variation 1827
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950846511"
variation 1829
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1313082363"
variation 1830
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1465200907"
variation 1831
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1357095646"
variation 1832
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:558156375"
variation 1839
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1363290036"
variation 1843
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="c"
/db_xref="dbSNP:1428595949"
variation 1850
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1423530802"
variation 1852
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1950846204"
exon 1853..1960
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/inference="alignment:Splign:2.1.0"
variation 1853
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1265969471"
variation 1857
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950758429"
variation 1858..1861
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="ag"
/replace="agag"
/db_xref="dbSNP:1950758380"
variation 1865
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:115684143"
variation 1866
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1222086097"
variation 1867
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950758289"
variation 1875
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:115566777"
variation 1876
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:758025460"
variation 1878
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:976650599"
variation 1879
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:747697880"
variation 1880
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:1566173893"
variation 1883
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1950757987"
variation 1886
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="aa"
/db_xref="dbSNP:2136917535"
variation 1886
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1356919481"
variation 1888
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:778392987"
variation 1889
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:754931883"
variation 1890
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1442480016"
variation 1899
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:937547511"
variation 1900
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:961309862"
variation 1901
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:557461509"
variation 1902
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1456695524"
variation 1904
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:766096241"
variation 1905
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:2136917474"
variation 1909
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:376798546"
variation 1910
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950757414"
variation 1914
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950757365"
variation 1915
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1439266364"
variation 1919
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:764448295"
variation 1920
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1950757240"
variation 1921
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1220708351"
variation 1923
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1195509679"
variation 1924
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:2136917397"
variation 1925
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:114483951"
variation 1926
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1950757063"
variation 1930
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:775769340"
variation 1931
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:144644143"
variation 1937
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950756927"
variation 1938
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1950756882"
variation 1950
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:373411620"
variation 1951
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:777155485"
variation 1957
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:76224039"
exon 1961..2033
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/inference="alignment:Splign:2.1.0"
variation 1965
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:772354359"
variation 1966
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:761464761"
variation 1967
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="t"
/replace="tt"
/db_xref="dbSNP:1476434657"
variation 1969
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1425682767"
variation 1972
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1593440414"
variation 1974
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1194364986"
variation 1980
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:774002945"
variation 1983
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1260717996"
variation 1984
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1212784968"
variation 1989
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:768078789"
variation 1990
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950735401"
variation 1996
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:192495200"
variation 1997
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:779420556"
variation 2000
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1950735266"
variation 2003..2007
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="gc"
/replace="gccgc"
/db_xref="dbSNP:1218603125"
variation 2005
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:769922499"
variation 2006
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:745735958"
variation 2009
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1339131647"
variation 2012
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:1188833829"
variation 2013
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950735030"
variation 2014
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1295444518"
variation 2016
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1449229353"
variation 2021
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1950734903"
variation 2022
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1340024053"
variation 2025
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950734826"
variation 2028
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:146332668"
variation 2029
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:371841032"
variation 2031
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1401175113"
variation 2032
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:752894210"
variation 2033
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:779235326"
exon 2034..3278
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/inference="alignment:Splign:2.1.0"
variation 2040
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1456116703"
variation 2042
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:549826875"
variation 2044
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1950704889"
variation 2045
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1223009144"
variation 2046
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:772496941"
variation 2049
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1950704757"
variation 2053
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1950704725"
variation 2054
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950704692"
variation 2059
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1288110354"
variation 2060
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1190631767"
variation 2064
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:200441646"
variation 2072
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2136907624"
variation 2076
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:1950704521"
variation 2077
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1242787279"
variation 2078
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950704441"
variation 2084
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:776670620"
variation 2085
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:770961851"
variation 2087
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1566171705"
variation 2088
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1238046110"
variation 2091
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:746869999"
variation 2092
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:777416500"
variation 2093
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:755292850"
variation 2094
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:973123804"
variation 2096
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:375664747"
variation 2099..2101
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="tt"
/replace="ttt"
/db_xref="dbSNP:1566171684"
variation 2102
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:780118329"
variation 2106
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1293032557"
variation 2107
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:756135373"
variation 2108..2109
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="tg"
/db_xref="dbSNP:1950704004"
variation 2113
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:750955936"
variation 2114
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1157735470"
variation 2115
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:531300162"
variation 2118
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:757695645"
variation 2119
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:113800546"
variation 2122
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:752032125"
variation 2123
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:549782692"
variation 2124
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:762683133"
variation 2141
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1314603974"
variation 2142
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950703637"
variation 2145..2146
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="aa"
/replace="aaa"
/db_xref="dbSNP:1950703539"
variation 2145
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:1353651008"
variation 2146
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1286369531"
variation 2147
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1045979"
variation 2150
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:954494653"
variation 2151
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:749186808"
variation 2153
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1283042988"
variation 2156
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1237120100"
variation 2157
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1348995249"
variation 2158
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2136907397"
variation 2159
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1593437486"
variation 2162
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1030178377"
variation 2167
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="a"
/db_xref="dbSNP:1950703000"
variation 2168
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="g"
/db_xref="dbSNP:1950702946"
variation 2169..2173
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="ccccc"
/replace="ccccccc"
/db_xref="dbSNP:1950702782"
variation 2170
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1950702902"
variation 2171
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1950702832"
variation 2174
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:925838751"
variation 2177
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1361292300"
variation 2179
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1593437462"
variation 2183
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:974644686"
variation 2185..2189
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="acgca"
/db_xref="dbSNP:1950702436"
variation 2186
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:567430632"
variation 2187
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1341331550"
variation 2191
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:911586191"
variation 2194
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:542153503"
variation 2197
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1156419163"
variation 2198
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1435059615"
variation 2199
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1593437426"
variation 2201
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:370209943"
variation 2203
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:950536054"
variation 2204
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950702021"
variation 2208
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:559705268"
variation 2210
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1010901456"
variation 2213
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950701848"
variation 2214
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1298882440"
variation 2216
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:893810615"
variation 2222
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:963549804"
variation 2230..2231
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="ct"
/replace="ctct"
/db_xref="dbSNP:2136907189"
variation 2231..2233
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="t"
/replace="ttt"
/replace="ttttt"
/db_xref="dbSNP:3832804"
variation 2231
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="t"
/replace="tgt"
/db_xref="dbSNP:2136907182"
variation 2232
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="t"
/replace="tat"
/db_xref="dbSNP:2136907172"
variation 2234
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1593437365"
variation 2235
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:111820152"
variation 2236
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1052601435"
variation 2237
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950701329"
variation 2238
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1414983132"
variation 2239
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950701238"
variation 2240
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="t"
/replace="tt"
/db_xref="dbSNP:1950701181"
variation 2244
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:935595520"
variation 2245..2248
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="gaga"
/replace="gagaga"
/db_xref="dbSNP:1950701113"
variation 2249..2251
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="cc"
/replace="ccc"
/db_xref="dbSNP:1418783722"
variation 2254
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950701021"
variation 2255
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1002477975"
variation 2262
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1278595598"
variation 2264
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1347878070"
variation 2265..2269
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="gggg"
/replace="ggggg"
/db_xref="dbSNP:1950700679"
variation 2265
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:541179525"
variation 2266
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1950700733"
variation 2269
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:576945941"
variation 2271
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:769326943"
variation 2272
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:892514179"
variation 2273
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1054288089"
variation 2278
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:367620504"
variation 2279
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:916367947"
variation 2282
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:973064787"
variation 2288
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1038910312"
variation 2289
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:963001005"
variation 2290..2291
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="cc"
/replace="ga"
/db_xref="dbSNP:796574941"
variation 2290
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950700117"
variation 2291
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:943323229"
variation 2293
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950699977"
variation 2294
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950699935"
variation 2298
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950699905"
variation 2301
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1950699872"
variation 2304
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:370314942"
variation 2305
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950699794"
variation 2306
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950699755"
variation 2307
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:182916402"
variation 2308
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:3741490"
variation 2313
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1443374356"
variation 2315
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950699663"
variation 2317
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2136906865"
variation 2319
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:983339952"
variation 2322
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:1950699592"
variation 2324
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1301770978"
variation 2330
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:987116079"
variation 2331
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950699497"
variation 2333
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:554895850"
variation 2335
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2136906816"
variation 2336
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950699427"
variation 2340
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1950699392"
variation 2345
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1298316988"
variation 2348
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950699320"
variation 2350
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:75237791"
variation 2351
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:746850522"
variation 2353
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1353265460"
variation 2354
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:777597930"
variation 2355
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:973165920"
variation 2359
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:758214417"
variation 2360
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:996057076"
variation 2362
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:192844482"
variation 2363..2367
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="gag"
/replace="gagag"
/db_xref="dbSNP:1423726431"
variation 2363
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:547619077"
variation 2369
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:2136906701"
variation 2371
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1010952147"
variation 2372
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1002451487"
variation 2375
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950698849"
variation 2378
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:893777773"
variation 2382
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1030977492"
variation 2384
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1163686844"
variation 2394
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950698740"
variation 2395
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1950698712"
variation 2396
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:781543889"
variation 2397
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:906815915"
variation 2398
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:2136906626"
variation 2401
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1415593537"
variation 2403
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1046993159"
variation 2413
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1334852400"
variation 2414
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:3741489"
variation 2420
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950698472"
variation 2423
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950698451"
variation 2424
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1270832087"
variation 2425
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1450666893"
variation 2427
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:4758909"
variation 2435
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1201112509"
variation 2438
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1192780707"
variation 2445
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1950698208"
variation 2449
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1258321216"
variation 2453
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:112870346"
variation 2455
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1593437106"
variation 2458
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1476204979"
variation 2459
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1163079471"
variation 2461
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1593437086"
variation 2464
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:754605513"
variation 2465
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:549889950"
variation 2468
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1458219528"
variation 2475
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1413405596"
variation 2476..2480
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="ag"
/replace="aggag"
/db_xref="dbSNP:1950697843"
variation 2483
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1037421988"
variation 2485..2487
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="gag"
/db_xref="dbSNP:1272645289"
variation 2485
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950697778"
variation 2489
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1053774837"
variation 2494
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1401470577"
variation 2498
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950697578"
variation 2499
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1231595234"
variation 2502
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1161815482"
variation 2507
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1950697422"
variation 2508
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1343788492"
variation 2509
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1593437040"
variation 2510
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:941773272"
variation 2511
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:907515157"
variation 2512
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:142376269"
variation 2515
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950697143"
variation 2517..2518
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="aa"
/replace="aaa"
/db_xref="dbSNP:36039891"
variation 2517
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950697092"
variation 2521
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950696998"
variation 2525
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1950696954"
variation 2528
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:933225060"
variation 2538
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1355291257"
variation 2540
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1223981564"
variation 2550
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:923251377"
variation 2551
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:1950696730"
variation 2552
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1950696680"
variation 2554
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:755120503"
variation 2555
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:2136906288"
variation 2557
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950696585"
variation 2558
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1566171220"
variation 2562
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:964542689"
variation 2566
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:1021425081"
variation 2572..2574
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="tt"
/replace="ttt"
/db_xref="dbSNP:1950696422"
variation 2572
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950696455"
variation 2579..2586
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="ctt"
/replace="cttatctt"
/db_xref="dbSNP:943198387"
variation 2579
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1950696399"
variation 2584
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:989498094"
variation 2589
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1215845332"
variation 2599
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950696268"
variation 2601
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1258077252"
variation 2602
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950696224"
variation 2603
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950696187"
variation 2605
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950696162"
variation 2607
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1296311836"
variation 2609
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2136906187"
variation 2613
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:958138392"
variation 2616
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950696070"
variation 2621..2627
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="aata"
/replace="aataata"
/db_xref="dbSNP:1950695982"
variation 2622..2631
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="ataat"
/replace="ataatataat"
/db_xref="dbSNP:1950695893"
variation 2624
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:1950696039"
variation 2626..2641
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="tataattta"
/replace="tataatttataattta"
/db_xref="dbSNP:1401013436"
variation 2626
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1486597998"
variation 2629
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950695953"
variation 2630
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:1593436977"
variation 2634
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950695859"
variation 2637
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1950695816"
variation 2638
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1030946220"
variation 2642
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950695735"
variation 2646
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1236969685"
variation 2649
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1950695685"
variation 2651
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:911779056"
variation 2652..2653
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="t"
/db_xref="dbSNP:1950695597"
variation 2652
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:1950695623"
variation 2653
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:1950695572"
variation 2654
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1179105860"
variation 2656
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1950695511"
variation 2658
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1406240647"
variation 2660
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:560709767"
variation 2661
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1950695431"
variation 2665
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:999568389"
variation 2667
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950695356"
variation 2669
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:548922117"
variation 2670
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1377843900"
variation 2671..2674
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="t"
/replace="tatt"
/db_xref="dbSNP:1950695202"
variation 2672
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:1950695263"
variation 2673
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950695232"
variation 2674..2677
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="ttga"
/db_xref="dbSNP:1950695140"
variation 2676
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1025188661"
variation 2677..2679
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="aa"
/replace="aaa"
/db_xref="dbSNP:1950695100"
variation 2685
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1331697816"
variation 2686
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:973134921"
variation 2687
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1012923039"
variation 2688
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:2136905955"
variation 2689
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950694997"
variation 2690
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:895287582"
variation 2692
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950694939"
variation 2693
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1950694917"
variation 2694
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2136905920"
variation 2695..2696
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="g"
/db_xref="dbSNP:34409499"
variation 2696
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1165063779"
variation 2701..2703
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="t"
/replace="tat"
/db_xref="dbSNP:1950694812"
variation 2702
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:2136905904"
variation 2703
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950694782"
variation 2705..2711
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="aaaaaaa"
/replace="aaaaaaaa"
/db_xref="dbSNP:1350044921"
variation 2705
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1374414628"
variation 2706
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:926776920"
variation 2711
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1280739400"
variation 2712
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1593436904"
variation 2715
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1593436894"
variation 2716
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:530330334"
variation 2717
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:971314022"
variation 2723
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1438398757"
variation 2724
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950694458"
variation 2738
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1950694435"
variation 2740
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1206923715"
variation 2741
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1231446323"
variation 2742
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1406251214"
variation 2744
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:941743070"
variation 2745
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950694296"
variation 2747
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:115799873"
variation 2748
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:541241838"
variation 2751
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950694155"
variation 2752
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:2136905761"
variation 2753
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950694126"
variation 2754
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950694099"
variation 2763
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1047424647"
variation 2765
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:932962176"
variation 2766
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:753996875"
variation 2767
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1211863620"
variation 2769
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950693980"
variation 2770
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1397721159"
variation 2771
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1489535422"
variation 2773
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1266210457"
variation 2776..2780
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="aaccg"
/db_xref="dbSNP:1950693729"
variation 2778..2779
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="atgctgctcccttgtgtgagtgaccacggccccgagcctggggctgga
cgcaggtcccagga"
/db_xref="dbSNP:1950693826"
variation 2778
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1316055975"
variation 2779..2780
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="acggccccgagcctggggctggacgcaggtcccaggacgtgct"
/db_xref="dbSNP:1441439409"
variation 2779
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:766575351"
variation 2780..2781
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="agcctggggctggacgcaggtcccaggacgtgctgctcccttct"
/replace="caggtcccaggacgtgctgctcccttct"
/replace="ctcccttct"
/replace="tgcattcccttct"
/replace="tgctgctcccttct"
/db_xref="dbSNP:rs1336309071"
variation 2781..2891
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="gtgagtgaccgcggccccgagcctggggctggacgcaggtcccaggac
"
/replace="gtgagtgaccgcggccccgagcctggggctggacgcaggtcccaggac
atgctgctcccttgtgtgagtgaccgcggccccgagcctggggctggacgcaggtccc
aggac"
/db_xref="dbSNP:1950691745"
variation 2781
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950693572"
variation 2781
/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 2782
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:974656529"
variation 2783
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1304579464"
variation 2786
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:1593436768"
variation 2788
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1593436758"
variation 2790
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:577007021"
variation 2791
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:60054929"
variation 2792..2828
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="cggccccgagcctggggctggacgcaggtcccaggac"
/replace="cggccccgagcctggggctggacgcaggtcccaggacgtgctgctccc
ttctgtgagtgaccacggccccgagcctggggctggacgcaggtcccaggac"
/db_xref="dbSNP:1566170955"
variation 2792
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:137860747"
variation 2793
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:543507917"
variation 2794
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1339972650"
variation 2796
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1950693259"
variation 2798
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:576425597"
variation 2799
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:978587251"
variation 2802..2803
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="cc"
/db_xref="dbSNP:1950693096"
variation 2802
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:970720837"
variation 2803
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950693066"
variation 2811
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1000902244"
variation 2814
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1025409954"
variation 2815
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1012477120"
variation 2816
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="cc"
/db_xref="dbSNP:1722609409"
variation 2821
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950692922"
variation 2822
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1452627569"
variation 2823
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1950692858"
variation 2825
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:899887350"
variation 2828
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950692769"
variation 2829
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:373137192"
variation 2830..2916
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="tgctgctcccttgtgtgagtgacc"
/replace="tgctgctcccttgtgtgagtgaccgcggccccgagcctggggctggac
gcaggtcccaggacgtgctgctcccttgtgtgagtgacc"
/db_xref="dbSNP:1950691334"
variation 2832
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:554677515"
variation 2835
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:377537751"
variation 2839
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1420814830"
variation 2841..2842
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="ac"
/db_xref="dbSNP:1950692612"
variation 2842
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:796139459"
variation 2843
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1006432643"
variation 2849
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1950692520"
variation 2852
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1396446600"
variation 2853..2854
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="acggccccgagcctggggctggacgcaggtcccaggacgtgctgctcc
cttctgtgagt"
/replace="acggccccgagcctggggctggacgcaggtcccaggacgtgctgctcc
cttctgtgagtgaccacggccccgagcctggggctggacgcaggtcccaggacatgct
gctcccttctgtgagt"
/replace="acggccccgagcctggggctggacgcaggtcccaggacgtgctgctcc
cttgtgtgagt"
/db_xref="dbSNP:1566170899"
variation 2853
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1384812230"
variation 2854..2855
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="acca"
/db_xref="dbSNP:1566170888"
variation 2854
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:15638"
variation 2855
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:111799372"
variation 2856
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:572274927"
variation 2858
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950692211"
variation 2859
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:997687935"
variation 2861
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:376925671"
variation 2862
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1039131607"
variation 2866
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950692083"
variation 2867..2917
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="tggggctggacgcaggtcccaggacgtgctgctcccttgtgtgagtga
cca"
/db_xref="dbSNP:1566170810"
variation 2867
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:373528706"
variation 2868
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1593436635"
variation 2872
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1354479573"
variation 2873
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="t"
/replace="tt"
/db_xref="dbSNP:1192334475"
variation 2877
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:369891917"
variation 2878
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1950691911"
variation 2879
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1950691881"
variation 2881
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1950691853"
variation 2882
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:867795922"
variation 2889
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:187667016"
variation 2891
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1186063298"
variation 2892
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:111786421"
variation 2893..2904
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="tgctgctccctt"
/replace="tgctgctcccttctgtgagtgaccacggccccgagcctggggctggac
gcaggtcccaggacatgctgctccctt"
/db_xref="dbSNP:1950691518"
variation 2893
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950691632"
variation 2895..2896
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="a"
/db_xref="dbSNP:1950691609"
variation 2897..2898
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="gc"
/db_xref="dbSNP:1950691577"
variation 2900
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1485012640"
variation 2904
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1054216011"
variation 2905
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:75167846"
variation 2908
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950691423"
variation 2909
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950691387"
variation 2912
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950691364"
variation 2917
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1456063340"
variation 2918
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:538873969"
variation 2919
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:117246365"
variation 2920..2932
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="gccccaagcccag"
/db_xref="dbSNP:1230976787"
variation 2920
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1566170789"
variation 2921
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950691154"
variation 2922
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950691128"
variation 2923
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1007364269"
variation 2924
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1218487646"
variation 2925
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:111338463"
variation 2926
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950690986"
variation 2930
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:978174785"
variation 2931
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:8021"
variation 2933
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:917908364"
variation 2938
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950690803"
variation 2940
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1332266605"
variation 2941
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:890301777"
variation 2942
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1301350623"
variation 2946
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1593436516"
variation 2948
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950690645"
variation 2951
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1950690593"
variation 2952
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1051667411"
variation 2953
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950690530"
variation 2954
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:991258229"
variation 2955
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:959608059"
variation 2956
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1016485269"
variation 2957
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1006486333"
variation 2959
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:73489148"
variation 2960
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950690229"
variation 2963
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1950690169"
variation 2964
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1364197764"
variation 2965
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1455110594"
variation 2973
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1026915435"
variation 2975
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1359866417"
variation 2976
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1566170710"
variation 2977
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1172254217"
variation 2978
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1468017193"
variation 2979
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1950689734"
variation 2980
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1376990440"
variation 2985
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950689662"
variation 2986
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:997254637"
variation 2989
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1395673079"
variation 2990
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1378783852"
variation 2995
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="cggtc"
/db_xref="dbSNP:1950689542"
variation 2998
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950689502"
variation 2999
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:941680964"
variation 3000
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="a"
/db_xref="dbSNP:2136904893"
variation 3002
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:535014873"
variation 3005
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1950689402"
variation 3010
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1950689380"
variation 3011
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950689346"
variation 3018..3030
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="tg"
/replace="tggcttccgcctg"
/db_xref="dbSNP:1950689207"
variation 3018
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:1238486499"
variation 3025
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1038687461"
variation 3026
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1007221366"
variation 3027
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:182104463"
variation 3030
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:980532486"
variation 3031
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1349314061"
variation 3033
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950689114"
variation 3035
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1213577280"
variation 3041
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1436173408"
variation 3043
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950689033"
variation 3044
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:764304023"
variation 3049
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2136904817"
variation 3052
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:566065778"
variation 3056
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1481966746"
variation 3059
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1950688911"
variation 3062
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2136904799"
variation 3063
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950688886"
variation 3067
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1950688853"
variation 3070
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1199546557"
variation 3073
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1950688798"
variation 3074
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:892808322"
variation 3075..3079
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="ttttt"
/replace="tttttt"
/db_xref="dbSNP:1950688694"
variation 3078
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:949556782"
variation 3080..3081
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="gg"
/db_xref="dbSNP:1176616028"
variation 3082..3089
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="aaaa"
/replace="aaaaaa"
/replace="aaaaaaa"
/replace="aaaaaaaa"
/replace="aaaaaaaaa"
/db_xref="dbSNP:rs957212862"
variation 3082
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1265543823"
variation 3083
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1054268966"
variation 3084
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:934594162"
variation 3085
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1488453973"
variation 3090
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:191072646"
variation 3091..3096
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="ttttt"
/replace="tttttt"
/replace="ttttttt"
/db_xref="dbSNP:1566170618"
variation 3093
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1256563011"
variation 3095..3101
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="tt"
/replace="ttatctt"
/db_xref="dbSNP:1950688278"
variation 3097
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:566122046"
variation 3100
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:949484292"
variation 3101
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1950688259"
variation 3102
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950688232"
variation 3114
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950688210"
variation 3115
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1018288530"
variation 3116
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1950688147"
variation 3117
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950688117"
variation 3122
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1299758456"
variation 3123
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:549120489"
variation 3131
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950688014"
variation 3136
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:918030300"
variation 3138
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:565128269"
variation 3142
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1458856890"
variation 3150..3157
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="cttct"
/replace="cttcttct"
/db_xref="dbSNP:1468716986"
variation 3151
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:937960418"
variation 3152
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:909224402"
variation 3153
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1226033314"
variation 3156
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1046106"
variation 3158
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950687714"
variation 3163
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1315555821"
variation 3164
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950687665"
variation 3165
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1279655347"
variation 3166
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1950687603"
variation 3167
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:985017981"
variation 3168
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1950687569"
variation 3175
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:1950687539"
variation 3176
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1432491382"
variation 3179
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:753726528"
variation 3181
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1950687442"
variation 3189
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1425798710"
variation 3191
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2136904528"
variation 3195
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950687386"
variation 3197
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:529547282"
variation 3200..3217
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="ctg"
/replace="ctgagaagcagcaatctg"
/db_xref="dbSNP:1950687169"
variation 3200
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:148270257"
variation 3202
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:11542904"
variation 3213
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:2136904496"
variation 3215
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:976689419"
variation 3216
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950687203"
variation 3217
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:2136904480"
variation 3218
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950687133"
variation 3219
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1950687101"
variation 3223
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:965819930"
variation 3225
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1950687045"
variation 3233
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="g"
/db_xref="dbSNP:897708347"
variation 3233
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1367604138"
variation 3236
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1037632913"
variation 3238
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950686909"
variation 3240
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950686881"
variation 3241
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950686849"
variation 3251
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:941651179"
variation 3252
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1046130"
regulatory 3254..3259
/regulatory_class="polyA_signal_sequence"
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
variation 3254
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1950686736"
variation 3255
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950686709"
variation 3260
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:904877930"
variation 3261
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1017734390"
variation 3265
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:376262240"
variation 3266
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1007273719"
variation 3267
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:892777244"
variation 3268
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:561407931"
variation 3272
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1244757352"
variation 3274
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1298125618"
variation 3275
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:998710936"
variation 3277
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950686377"
polyA_site 3278
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
ORIGIN
agctgagggagccgcaatgtctcttgacagcggcggcggcgcagccggttccgggttcggcgcggggcggggatgtgaatcccgatggagcggcccgaggaaggcaagcagtcgccgccgccgcagccctggggacggctcctgcgtctgggcgcggaggagggcgagccgcacgtcctcctgaggaagcgggagtggaccatcgggcggagacgaggttgcgacctttccttccccagcaataaactggtctctggagatcactgtagaattgtagtggatgaaaaatcaggtcaggtgacactggaagataccagcaccagtggaacagtgattaacaagctgaaggttgttaagaagcagacatgccctttacagactggggatgtcatctacttggtgtacaggaagaatgaaccggaacacaacgtggcatacctctatgaatctttaagtgaaaagcaaggcatgacacaagaatcctttgaagctaacaaggaaaatgtgttccatgggaccaaagatacctcaggtgcaggtgcagggcgaggggccgatccccgggtccctccgtcgtcgcccgccactcaggtgtgctttgaggaaccacagccatcaacatcgacgtcagacctcttccccacagcctcggcctcttccacggagccttctcctgcagggcgagagcgttcctccagttgtgggtctgggggtggtggcatctcccctaaaggaagtggtccctctgtggcaagtgatgaagtctccagctttgcctcagctctcccagacagaaagactgcgtccttttcgtcgttggaaccccaggatcaggaggatttggagcccgtgaagaagaaaatgagaggagatggggaccttgacctgaacgggcagttgttggtcgcacaaccgcgtagaaatgcccaaaccgtccacgaggacgtcagagcagcggctgggaagccagacaagatggaggagacgctgacatgcatcatctgccaggacctgctgcacgactgcgtgagtttgcagccctgcatgcacacgttctgcgcggcttgctactcgggctggatggagcgctcgtccctgtgtcctacctgccgctgtcccgtggagcggatctgtaaaaaccacatcctcaacaacctcgtggaagcatacctcatccagcatccagacaagagtcgcagtgaagaagatgtgcaaagtatggatgccaggaataaaatcactcaagacatgctgcagcccaaagtcaggcggtctttttctgatgaagaagggagttcagaggacctgctggagctgtcagacgttgacagtgagtcctcagacattagccagccatacgtcgtgtgccggcagtgtcctgagtacagaaggcaggcggcgcagcctccccactgcccagcacccgagggcgagccaggagccccacaggccctgggggatgcaccctccacgtccgtcagcctgacgacagtccaggattacgtgtgccctctgcaaggaagccacgccctgtgcacctgctgcttccagcccatgcccgaccggagagcggagcgcgagcaggacccgcgtgtcgcccctcagcagtgtgcggtctgcctgcagcctttctgccacctgtactggggctgcacccggaccggctgctacggctgcctggccccgttttgtgagctcaacctgggtgacaagtgtctggacggcgtgctgaacaacaacagctacgagtcagacatcctgaagaattacctggcaaccagaggtttgacatggaaaaacatgttgaccgagagcctcgtggctctccagcggggagtgtttctgctgtctgattacagagtcacgggagacaccgttctgtgttactgctgtggcctgcgcagcttccgtgagctgacctatcagtatcggcagaacattcctgcttccgagttgccagtggccgtaacatcccgtcctgactgctactggggccgtaactgccgcactcaggtgaaagctcaccacgccatgaaattcaatcatatctgtgaacagacaaggttcaaaaactaagcatccagaggccctgagcagctttcagcactggaggtgaagagagcgtgtttttaaaatacagagacaagcacgtcaaggtgttttcacagccccctgagggaagggacgcagggtctccgacaggtgctctggggtgactcttctgtggagctttaccctctgagtgagaccctccccagagccccgggggccgcagcccgccctcctggtgagcgctgggcagggctcgtggtggcatcagcagcagagacgaagcctttctgtaacatgcggccgtcccgccgagaggggcagttttgctcttttgtacattttccgaaactacagttaaagcagaagtctgtttttaggaaaagtttcaagggagaagggcaagtttatcaaaaacattgtttcaggagaagggagcataagtttacagcctacaggacgtacacaatatcctgctgctgggaaaaccacagcattttatctattttttattttaataggtttggtgcttatcttctaataagatttaaatgtcacaaactgtagcacaaataatataatttataatttacaaattgactaaaattgggtatagtatggtatttgaaagaataagcatatgcttctgtttattaaaaaaagaaaccttccaatgtccaaaactgctaaccctcgacgtggccgccaagttagtcgctccttgctaaccggtgagtgaccgcggccccgagcctggggctggacgcaggtcccaggacatgctgctcccttgtgtgagtgaccgcggccccgagcctggggctggacgcaggtcccaggacgtgctgctcccttgtgtgagtgaccacggccccaagcccagggctggaggcaggtcccaggacgcgccgctccctcatgctgcccgggcccttcctccaagaccctacagagcctgaggggcaccttggcttccgcctgtgctagctttgccatgtcatctggaataatacttgaaattttgatttttggaaaaaaaagttttttatcttttgttgaaatcacctgttatccttgtttgtaaactgataacttttttgcttcttctcaggaatacagttttcaactgttgtcttgctcttgatagaaactgagaagcagcaatctgtatttgtggaggaaagtcctctcttttgcatattctaataaatgagccgcgtttgctcctcaaaaaaaaaa
//
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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