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Previous release (v1)
2024-04-20 14:37:33, GGRNA.v2 : RefSeq release 222 (Jan, 2024)
LOCUS NM_018223 3168 bp mRNA linear PRI 17-APR-2023
DEFINITION Homo sapiens checkpoint with forkhead and ring finger domains
(CHFR), transcript variant 4, mRNA.
ACCESSION NM_018223
VERSION NM_018223.2
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 3168)
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 3168)
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 3168)
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 3168)
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 3168)
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 3168)
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 3168)
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 3168)
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 3168)
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 3168)
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, AK001658.1,
AK027687.1, AC127070.10 and BC012072.1.
On Jun 6, 2009 this sequence version replaced NM_018223.1.
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 :: AK001658.1, SRR1660809.224931.1
[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
1-20 BP313700.1 1-20
21-727 AK001658.1 1-707
728-728 AK027687.1 809-809
729-1344 AK001658.1 709-1324
1345-1345 AK027687.1 1426-1426
1346-1810 AK001658.1 1326-1790
1811-2113 AK027687.1 1892-2194
2114-2811 AC127070.10 108422-109119
2812-3168 BC012072.1 2825-3181
FEATURES Location/Qualifiers
source 1..3168
/organism="Homo sapiens"
/mol_type="mRNA"
/db_xref="taxon:9606"
/chromosome="12"
/map="12q24.33"
gene 1..3168
/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..1956
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/EC_number="2.3.2.27"
/note="isoform 4 is encoded by transcript variant 4; 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 4"
/protein_id="NP_060693.2"
/db_xref="CCDS:CCDS31937.1"
/db_xref="GeneID:55743"
/db_xref="HGNC:HGNC:20455"
/db_xref="MIM:605209"
/translation="
MERPEEGKQSPPPQPWGRLLRLGAEEGEPHVLLRKREWTIGRRRGCDLSFPSNKLVSGDHCRIVVDEKSGQVTLEDTSTSGTVINKLKVVKKQTCPLQTGDVIYLVYRKNEPEHNVAYLYESLSEKQGMTQESFEMVPCCVAQAGLKLLGSSDPPTLASQSIVITGSGGGGISPKGSGPSVASDEVSSFASALPDRKTASFSSLEPQDQEDLEPVKKKMRGDGDLDLNGQLLVAQPRRNAQTVHEDVRAAAGKPDKMEETLTCIICQDLLHDCVSLQPCMHTFCAACYSGWMERSSLCPTCRCPVERICKNHILNNLVEAYLIQHPDKSRSEEDVQSMDARNKITQDMLQPKVRRSFSDEEGSSEDLLELSDVDSESSDISQPYVVCRQCPEYRRQAAQPPHCPAPEGEPGAPQALGDAPSTSVSLTTAVQDYVCPLQGSHALCTCCFQPMPDRRAEREQDPRVAPQQCAVCLQPFCHLYWGCTRTGCYGCLAPFCELNLGDKCLDGVLNNNSYESDILKNYLATRGLTWKNMLTESLVALQRGVFLLSDYRVTGDTVLCYCCGLRSFRELTYQYRQNIPASELPVAVTSRPDCYWGRNCRTQVKAHHAMKFNHICEQTRFKN"
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 853..>1467
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/note="DNA repair protein rad18; Region: rad18; TIGR00599"
/db_xref="CDD:273165"
misc_feature 859..1020
/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 1351..1821
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/note="Cysteine rich domain with multizinc binding
regions; Region: zf-CRD; pfam17979"
/db_xref="CDD:436187"
misc_feature 1855..1926
/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..580
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/inference="alignment:Splign:2.1.0"
variation 491
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1331574821"
variation 493
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1349750283"
variation 496
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1180972611"
variation 497
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:9943856"
variation 500
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:771714333"
variation 501
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:747621911"
variation 503
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1159355477"
variation 505
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:139045656"
variation 506
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1225701393"
variation 511
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1951231839"
variation 512
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:770802724"
variation 514
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:113941471"
variation 516
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1200997859"
variation 518
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1478094317"
variation 525
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:1238108509"
variation 526..530
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="ct"
/replace="ctcct"
/db_xref="dbSNP:1216434365"
variation 526
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:749243668"
variation 529
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1643249948"
variation 530
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1004863721"
variation 532
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1249948248"
variation 533
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1449096307"
variation 534
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:890489027"
variation 537..538
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="aa"
/db_xref="dbSNP:1951231070"
variation 539
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:536448896"
variation 542
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:912312301"
variation 544
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1386156952"
variation 547
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1208289168"
variation 551
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1327378162"
variation 554
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1161754439"
variation 555
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1052427155"
variation 556
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1265270599"
variation 558
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1413566399"
variation 560
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1224174923"
variation 562
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1951230432"
variation 563
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1951230365"
variation 565
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1344471837"
variation 566
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1390162710"
variation 567
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1274177364"
variation 570
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:932290965"
variation 571
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1434216915"
variation 573
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:190910189"
variation 574
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1321004658"
variation 578
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1951229911"
variation 579
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1951229858"
variation 580
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1319461623"
exon 581..748
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/inference="alignment:Splign:2.1.0"
variation 584
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1038150337"
variation 586
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:370517411"
variation 587
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1951211639"
variation 589
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1438318944"
variation 590
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:777186106"
variation 592..593
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="gg"
/db_xref="dbSNP:1189456093"
variation 592
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:766667278"
variation 595
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:761034338"
variation 596
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1593482765"
variation 598
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:138637226"
variation 600
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1951211154"
variation 601
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1387477118"
variation 604
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:34220055"
variation 605
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:761525824"
variation 606
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2136982888"
variation 611
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1951210868"
variation 614
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:774070010"
variation 615
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:1419993206"
variation 616
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1951210693"
variation 617
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:201192149"
variation 618
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:989203291"
variation 620
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1951210512"
variation 624
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:796201985"
variation 625
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1163339779"
variation 633
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:749192848"
variation 637
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:374107669"
variation 639
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:769505625"
variation 644
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:780945230"
variation 648
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1951210091"
variation 657
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1951210040"
variation 661
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:35206714"
variation 663
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1951209926"
variation 664
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1366834805"
variation 666
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1038008124"
variation 668
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:560433355"
variation 670..676
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="aga"
/replace="agaaaga"
/db_xref="dbSNP:1951209560"
variation 673
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:201727566"
variation 677
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:2136982730"
variation 678
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:758662673"
variation 679
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:533118486"
variation 680
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:150995074"
variation 681
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:755027328"
variation 682..686
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="t"
/replace="tcctt"
/db_xref="dbSNP:2136982677"
variation 684
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:908433616"
variation 687
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:200213031"
variation 689
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:754307363"
variation 690
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:145246258"
variation 692
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:141183005"
variation 693
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:767988129"
variation 694..695
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="t"
/replace="tt"
/db_xref="dbSNP:766718829"
variation 696
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1566189184"
variation 697
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1423637297"
variation 700..703
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="ccc"
/replace="cccc"
/db_xref="dbSNP:762524769"
variation 700
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:751592981"
variation 702
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1951208832"
variation 704
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:373754363"
variation 705
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:761615752"
variation 706
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:147803776"
variation 708
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1566189143"
variation 710
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1951208615"
variation 714
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:774088595"
variation 715
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1472958431"
variation 723
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:768052255"
variation 724..726
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="cc"
/replace="ccc"
/db_xref="dbSNP:2136982524"
variation 725
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:762481129"
variation 726
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1025589682"
variation 727
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:775309126"
variation 729
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:764279540"
variation 730
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1951208249"
variation 731
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1463671908"
variation 733
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:974854406"
variation 736
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:1221100387"
variation 737
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1951208117"
variation 738
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:1238379063"
variation 739
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1951208036"
variation 740
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1566189061"
variation 745
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:745763828"
exon 749..908
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/inference="alignment:Splign:2.1.0"
variation 749
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1951157533"
variation 750
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:756088633"
variation 753
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1951157390"
variation 754
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:563202190"
variation 757
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2136974267"
variation 758
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1360404336"
variation 761
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1951157150"
variation 762
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:781748631"
variation 765
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:757715316"
variation 767
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:752016583"
variation 768
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:377318460"
variation 769
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:115096950"
variation 770
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1593477819"
variation 771
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1393923793"
variation 772..773
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="t"
/db_xref="dbSNP:776753889"
variation 773
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:1311480210"
variation 774
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:758139441"
variation 775
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:973250523"
variation 777
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1021390710"
variation 781
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:752281100"
variation 783
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:115431373"
variation 784
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:148618944"
variation 786
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:369526598"
variation 789
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:769878915"
variation 790
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:540759128"
variation 791
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:760584451"
variation 792
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:773102049"
variation 793
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:749537035"
variation 794
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:375174098"
variation 796
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:770024903"
variation 799
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1951155348"
variation 802
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:188170704"
variation 803
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:745889598"
variation 804
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1951155139"
variation 805
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:781395404"
variation 807
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:757876886"
variation 808
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1593477690"
variation 809
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1951154950"
variation 810
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:747517165"
variation 811
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:199761208"
variation 814
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1951154859"
variation 816
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1380131918"
variation 817
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:144838296"
variation 819
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1449844658"
variation 821
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1000960906"
variation 822
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:371434249"
variation 823
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:764757412"
variation 824
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="t"
/db_xref="dbSNP:768680290"
variation 824
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1464052810"
variation 826
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:754506935"
variation 827
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:149862277"
variation 830
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2136973920"
variation 831
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:765845584"
variation 833
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1277312621"
variation 834
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:746414469"
variation 835
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1341883561"
variation 836
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:2136973888"
variation 837
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1295926976"
variation 839
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1306779303"
variation 841
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1593477559"
variation 842
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1375950961"
variation 845
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2136973857"
variation 846
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:35011845"
variation 847
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1341253353"
variation 849
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1951153923"
variation 852
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1312306793"
variation 853
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:767348322"
variation 855
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1352413194"
variation 858
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2136973793"
variation 861
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:2136973786"
variation 863
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:761474515"
variation 864
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:775799321"
variation 865
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2136973760"
variation 867
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1951153687"
variation 868
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1951153632"
variation 870
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1369689338"
variation 872
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2136973741"
variation 874
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1951153534"
variation 876
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:770185579"
variation 877
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1252007101"
variation 879
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:12315353"
variation 882
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:146107503"
variation 888
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1368629651"
variation 891
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1186411942"
variation 892
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1951153233"
variation 893
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:759798633"
variation 894
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:2136973671"
variation 895
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1951153155"
variation 897
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1253421391"
variation 898
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1951153058"
variation 903
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:776915637"
variation 904
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:771123706"
variation 906
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1469130916"
exon 909..1063
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/inference="alignment:Splign:2.1.0"
variation 909
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:560066373"
variation 913
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1213141444"
variation 917
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:780721649"
variation 918
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:565644778"
variation 922
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:987211916"
variation 925
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1566185781"
variation 926
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1174814592"
variation 927
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1478670195"
variation 929
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:751498855"
variation 930
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:142975525"
variation 933
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1466544467"
variation 936
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:138280939"
variation 937
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:754144763"
variation 938
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:921635691"
variation 939
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:766660009"
variation 940
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:760933260"
variation 941
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1221124973"
variation 947
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:368405665"
variation 948
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:767634272"
variation 950
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:762287710"
variation 951
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1367099211"
variation 953
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:774770261"
variation 954
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1951109519"
variation 958
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1433978124"
variation 960
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:553735979"
variation 961..963
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="gag"
/replace="gagag"
/db_xref="dbSNP:1566185670"
variation 962
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:968563777"
variation 964
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:749601873"
variation 965
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:775805064"
variation 968
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1402056016"
variation 969
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:769371058"
variation 970
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1593473549"
variation 972
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:745529097"
variation 973..974
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="ct"
/db_xref="dbSNP:1951108714"
variation 976
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1951108652"
variation 978
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:780623191"
variation 982
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:535313174"
variation 983
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:756736276"
variation 985
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1474574138"
variation 988
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:770034782"
variation 989
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:146343801"
variation 992
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1441931198"
variation 994
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:571101753"
variation 996
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:115029653"
variation 997
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1344021759"
variation 1003
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:182092641"
variation 1004
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:756361707"
variation 1008
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1359376881"
variation 1010
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:141404869"
variation 1012
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1951107709"
variation 1013
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:767497782"
variation 1015
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1313496770"
variation 1016
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1319716667"
variation 1017
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1339366523"
variation 1019
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1951107360"
variation 1020
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1951107293"
variation 1023
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:375199215"
variation 1028
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:774858017"
variation 1029
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1951107092"
variation 1030
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1371529354"
variation 1031
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:764629991"
variation 1033
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1255988921"
variation 1035
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:191062458"
variation 1036
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:775898959"
variation 1039
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1182669640"
variation 1042
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1213131732"
variation 1043
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1241168194"
variation 1046
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1593473382"
variation 1047
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:148311652"
variation 1050
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:143181439"
variation 1051
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1241159400"
variation 1052
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1593473335"
variation 1053
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:770380694"
variation 1057
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:746470663"
variation 1058
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:370386571"
variation 1059
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2136966487"
variation 1061
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1951106171"
exon 1064..1226
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/inference="alignment:Splign:2.1.0"
variation 1065
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1227736511"
variation 1066..1067
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="aa"
/db_xref="dbSNP:777961507"
variation 1072
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1210874026"
variation 1074
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:928539042"
variation 1078..1085
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="gaaga"
/replace="gaagaaga"
/db_xref="dbSNP:1951075030"
variation 1078
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1951075098"
variation 1080
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1566184554"
variation 1087
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:879123151"
variation 1089
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1229649968"
variation 1091
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:777930523"
variation 1092
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1566184534"
variation 1094
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1293723698"
variation 1096
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:377225060"
variation 1100
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:748309050"
variation 1101
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:778828908"
variation 1102
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1434082116"
variation 1103
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:200764395"
variation 1104
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:369063253"
variation 1105
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:1026572995"
variation 1106
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:766865645"
variation 1107
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:2062163"
variation 1115
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1047280041"
variation 1116
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:750119581"
variation 1118
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:760238279"
variation 1120
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:761337268"
variation 1126
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:150467142"
variation 1134
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:763498728"
variation 1138
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1951074170"
variation 1143
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:930183182"
variation 1144
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1322357484"
variation 1145
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:762961678"
variation 1146
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:879252133"
variation 1147
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:920205326"
variation 1148
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:201828860"
variation 1150
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1593470536"
variation 1151
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:769607729"
variation 1152
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:745615761"
variation 1155
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:776390811"
variation 1159
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:974463026"
variation 1162..1168
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="gaag"
/replace="gaagaag"
/db_xref="dbSNP:1434190222"
variation 1169
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:772321674"
variation 1172
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1315657949"
variation 1175
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="cc"
/db_xref="dbSNP:1951073572"
variation 1175
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1413044699"
variation 1179
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1353432969"
variation 1183
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1951073448"
variation 1186
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1309789349"
variation 1191
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:748314312"
variation 1197
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1283784330"
variation 1198
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1951073286"
variation 1200
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1395585538"
variation 1201
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1165776578"
variation 1207
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1951073172"
variation 1209
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1951073138"
variation 1211
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:779111370"
variation 1212
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1951073053"
variation 1215
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1368718436"
variation 1217
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1951072973"
variation 1224
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:754958760"
exon 1227..1369
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/inference="alignment:Splign:2.1.0"
variation 1230
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1286314037"
variation 1231
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1020597739"
variation 1233
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:748419509"
variation 1234
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:372270460"
variation 1235
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1013270057"
variation 1236
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1438322046"
variation 1237
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:768814594"
variation 1238
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1318363216"
variation 1239
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:749373830"
variation 1240
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:150627547"
variation 1242
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:368755833"
variation 1246
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1435723841"
variation 1247
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:746360566"
variation 1248
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1191956640"
variation 1254
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1451601823"
variation 1256
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:781699438"
variation 1259
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:757496767"
variation 1263
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1192492326"
variation 1265
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950995102"
variation 1267
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1445358565"
variation 1268
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950994995"
variation 1274
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:374229656"
variation 1275
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:777240371"
variation 1276
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1303770543"
variation 1277
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:371541325"
variation 1278
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:563852229"
variation 1282
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1231849613"
variation 1283
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1950994654"
variation 1285
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1366854652"
variation 1286
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1270421677"
variation 1287
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1429332642"
variation 1289
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1176161885"
variation 1290
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:764723102"
variation 1296
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2136951422"
variation 1300
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1237028076"
variation 1302
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:759529335"
variation 1303
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:753721064"
variation 1305
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1375184437"
variation 1306
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950993996"
variation 1307
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:367968934"
variation 1308
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:374006779"
variation 1309
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:774658371"
variation 1310
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1167629443"
variation 1311
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1566181842"
variation 1312
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:924051400"
variation 1313
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1593463729"
variation 1314
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1041545091"
variation 1318
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:768798394"
variation 1320
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1239336733"
variation 1325
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950993248"
variation 1333
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950993189"
variation 1335
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1189940191"
variation 1338
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950993053"
variation 1340
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:138207644"
variation 1341
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1593463695"
variation 1342
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1256747525"
variation 1344
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1379314322"
variation 1345
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:775767314"
variation 1348
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1196421815"
variation 1349
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:769933100"
variation 1350
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:746380972"
variation 1351
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:1215461680"
variation 1353
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:781511228"
variation 1354
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:141835819"
variation 1358
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:747380214"
variation 1361
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:778169456"
variation 1363
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:1355326421"
variation 1364
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:752333209"
variation 1365
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:536396076"
exon 1370..1489
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/inference="alignment:Splign:2.1.0"
variation 1370
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1402157616"
variation 1371
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:757077660"
variation 1372
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1950950768"
variation 1374
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:146976267"
variation 1376
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:765605647"
variation 1377
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1408464611"
variation 1381
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2136945225"
variation 1383
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:141349945"
variation 1384
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:776642806"
variation 1388
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1593459784"
variation 1389
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1306934237"
variation 1390
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:764423128"
variation 1391
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1950950185"
variation 1393
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:766469365"
variation 1395
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:761102171"
variation 1396
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2136945164"
variation 1400
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1304421220"
variation 1404
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:773703522"
variation 1405
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:772460210"
variation 1407
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:147791929"
variation 1408
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1454391193"
variation 1412
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1345653105"
variation 1413
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:116286061"
variation 1416
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:768361418"
variation 1417
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1593459724"
variation 1418
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1396714833"
variation 1419..1426
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="ctgct"
/replace="ctgctgct"
/db_xref="dbSNP:1363396811"
variation 1419
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:748952886"
variation 1420
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:763257394"
variation 1422
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1278317795"
variation 1428
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1950949058"
variation 1429
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1593459675"
variation 1430
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:779441212"
variation 1431
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:775978433"
variation 1438
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1187706335"
variation 1440
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:781224248"
variation 1441
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:757239007"
variation 1442
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1593459653"
variation 1444
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:936864653"
variation 1445
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:969442993"
variation 1448
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:751440176"
variation 1450
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1950948312"
variation 1451
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2306541"
variation 1452
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:755310429"
variation 1453
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1298012137"
variation 1455
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950947947"
variation 1456
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:754035414"
variation 1457
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:944300584"
variation 1458
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:766376169"
variation 1459
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:150920425"
variation 1462
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1015010652"
variation 1463
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:773617183"
variation 1465
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950947517"
variation 1467
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2136944907"
variation 1469
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:768065335"
variation 1470
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:142511371"
variation 1471
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:114117795"
variation 1472..1475
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="gt"
/replace="gtgt"
/db_xref="dbSNP:1950947070"
variation 1472
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:201454195"
variation 1473
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1172173801"
variation 1474
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:200436687"
variation 1476
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:920038038"
variation 1477
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:746554223"
variation 1479
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:973207321"
variation 1483
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1486915053"
variation 1485
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1346472721"
variation 1486
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1258850426"
variation 1488
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:769207559"
exon 1490..1573
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/inference="alignment:Splign:2.1.0"
variation 1492
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:372012714"
variation 1493
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:201350082"
variation 1494
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:7975454"
variation 1497
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:375656978"
variation 1503
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1335016856"
variation 1505
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:201237898"
variation 1506
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1442703181"
variation 1507
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:765505226"
variation 1508
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1324580295"
variation 1512
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950877727"
variation 1514
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950877687"
variation 1515
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950877658"
variation 1517
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1403110794"
variation 1524
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:759242088"
variation 1526..1529
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="ggg"
/replace="gggg"
/db_xref="dbSNP:1950877531"
variation 1529
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:953787024"
variation 1533
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:546055046"
variation 1534
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1593453012"
variation 1535
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:766020195"
variation 1537
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:371092913"
variation 1538
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:146156998"
variation 1539
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1454840670"
variation 1540
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:979112170"
variation 1541
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1252629926"
variation 1542
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:772089817"
variation 1543
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1448818469"
variation 1545
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1593452935"
variation 1546
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1950876982"
variation 1548
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1249069969"
variation 1550
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:767140702"
variation 1551
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:765611625"
variation 1552
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1349644861"
variation 1557
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:189987561"
variation 1558
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1236250946"
variation 1560
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:966632867"
variation 1563
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950876673"
variation 1564
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1348083185"
variation 1565
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1302248351"
variation 1566
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1433674477"
variation 1569
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1327743680"
exon 1574..1644
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/inference="alignment:Splign:2.1.0"
variation 1575
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:777921940"
variation 1580
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1950866672"
variation 1581
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:200853567"
variation 1584
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:748721756"
variation 1585
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1179840200"
variation 1587
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950866525"
variation 1588
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950866486"
variation 1590
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1471040037"
variation 1591
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:1950866384"
variation 1593
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1415191475"
variation 1595
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1233090445"
variation 1602
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:372404283"
variation 1603
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:755522022"
variation 1604
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:754297675"
variation 1605
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1323808548"
variation 1612..1621
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="aacaaca"
/replace="aacaacaaca"
/db_xref="dbSNP:1950865942"
variation 1614
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1213796881"
variation 1615
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:780565079"
variation 1616
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1288355908"
variation 1619
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1225827826"
variation 1620
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:755891788"
variation 1622
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1288380542"
variation 1626
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:749973618"
variation 1627
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950865817"
variation 1628
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:1379904886"
variation 1629
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:767082498"
variation 1633
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1950865707"
variation 1634
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:1950865670"
variation 1635
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1416698488"
variation 1639
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:761176081"
variation 1644
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1326600805"
exon 1645..1732
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/inference="alignment:Splign:2.1.0"
variation 1646
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1432073088"
variation 1647
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950847784"
variation 1650
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1422500887"
variation 1651
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:899072283"
variation 1652
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1008556440"
variation 1655
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950847611"
variation 1657
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:776466473"
variation 1659
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1950847509"
variation 1661
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:576074865"
variation 1663..1674
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="gg"
/replace="ggtttgacatgg"
/db_xref="dbSNP:1950847213"
variation 1666
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:2306537"
variation 1671
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:536151635"
variation 1672
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1281285798"
variation 1673
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1378971375"
variation 1675..1679
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="aaaaa"
/replace="aaaaaa"
/db_xref="dbSNP:1224656808"
variation 1679
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1232869629"
variation 1681
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:200187965"
variation 1687
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:2136929281"
variation 1689
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:749821203"
variation 1690
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:780655269"
variation 1696
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:770399858"
variation 1698
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:899313894"
variation 1699
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2306536"
variation 1702
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1485801990"
variation 1703
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:781614371"
variation 1704
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:756917083"
variation 1707
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950846511"
variation 1709
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1313082363"
variation 1710
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1465200907"
variation 1711
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1357095646"
variation 1712
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:558156375"
variation 1719
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1363290036"
variation 1723
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="c"
/db_xref="dbSNP:1428595949"
variation 1730
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1423530802"
variation 1732
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1950846204"
exon 1733..1840
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/inference="alignment:Splign:2.1.0"
variation 1733
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1265969471"
variation 1737
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950758429"
variation 1738..1741
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="ag"
/replace="agag"
/db_xref="dbSNP:1950758380"
variation 1745
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:115684143"
variation 1746
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1222086097"
variation 1747
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950758289"
variation 1755
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:115566777"
variation 1756
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:758025460"
variation 1758
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:976650599"
variation 1759
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:747697880"
variation 1760
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:1566173893"
variation 1763
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1950757987"
variation 1766
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="aa"
/db_xref="dbSNP:2136917535"
variation 1766
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1356919481"
variation 1768
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:778392987"
variation 1769
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:754931883"
variation 1770
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1442480016"
variation 1779
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:937547511"
variation 1780
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:961309862"
variation 1781
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:557461509"
variation 1782
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1456695524"
variation 1784
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:766096241"
variation 1785
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:2136917474"
variation 1789
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:376798546"
variation 1790
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950757414"
variation 1794
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950757365"
variation 1795
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1439266364"
variation 1799
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:764448295"
variation 1800
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1950757240"
variation 1801
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1220708351"
variation 1803
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1195509679"
variation 1804
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:2136917397"
variation 1805
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:114483951"
variation 1806
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1950757063"
variation 1810
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:775769340"
variation 1811
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:144644143"
variation 1817
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950756927"
variation 1818
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1950756882"
variation 1830
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:373411620"
variation 1831
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:777155485"
variation 1837
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:76224039"
exon 1841..1913
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/inference="alignment:Splign:2.1.0"
variation 1845
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:772354359"
variation 1846
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:761464761"
variation 1847
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="t"
/replace="tt"
/db_xref="dbSNP:1476434657"
variation 1849
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1425682767"
variation 1852
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1593440414"
variation 1854
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1194364986"
variation 1860
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:774002945"
variation 1863
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1260717996"
variation 1864
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1212784968"
variation 1869
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:768078789"
variation 1870
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950735401"
variation 1876
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:192495200"
variation 1877
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:779420556"
variation 1880
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1950735266"
variation 1883..1887
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="gc"
/replace="gccgc"
/db_xref="dbSNP:1218603125"
variation 1885
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:769922499"
variation 1886
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:745735958"
variation 1889
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1339131647"
variation 1892
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:1188833829"
variation 1893
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950735030"
variation 1894
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1295444518"
variation 1896
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1449229353"
variation 1901
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1950734903"
variation 1902
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1340024053"
variation 1905
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950734826"
variation 1908
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:146332668"
variation 1909
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:371841032"
variation 1911
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1401175113"
variation 1912
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:752894210"
variation 1913
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:779235326"
exon 1914..3158
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/inference="alignment:Splign:2.1.0"
variation 1920
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1456116703"
variation 1922
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:549826875"
variation 1924
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1950704889"
variation 1925
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1223009144"
variation 1926
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:772496941"
variation 1929
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1950704757"
variation 1933
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1950704725"
variation 1934
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950704692"
variation 1939
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1288110354"
variation 1940
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1190631767"
variation 1944
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:200441646"
variation 1952
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2136907624"
variation 1956
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:1950704521"
variation 1957
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1242787279"
variation 1958
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950704441"
variation 1964
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:776670620"
variation 1965
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:770961851"
variation 1967
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1566171705"
variation 1968
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1238046110"
variation 1971
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:746869999"
variation 1972
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:777416500"
variation 1973
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:755292850"
variation 1974
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:973123804"
variation 1976
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:375664747"
variation 1979..1981
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="tt"
/replace="ttt"
/db_xref="dbSNP:1566171684"
variation 1982
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:780118329"
variation 1986
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1293032557"
variation 1987
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:756135373"
variation 1988..1989
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="tg"
/db_xref="dbSNP:1950704004"
variation 1993
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:750955936"
variation 1994
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1157735470"
variation 1995
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:531300162"
variation 1998
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:757695645"
variation 1999
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:113800546"
variation 2002
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:752032125"
variation 2003
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:549782692"
variation 2004
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:762683133"
variation 2021
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1314603974"
variation 2022
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950703637"
variation 2025..2026
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="aa"
/replace="aaa"
/db_xref="dbSNP:1950703539"
variation 2025
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:1353651008"
variation 2026
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1286369531"
variation 2027
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1045979"
variation 2030
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:954494653"
variation 2031
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:749186808"
variation 2033
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1283042988"
variation 2036
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1237120100"
variation 2037
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1348995249"
variation 2038
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2136907397"
variation 2039
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1593437486"
variation 2042
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1030178377"
variation 2047
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="a"
/db_xref="dbSNP:1950703000"
variation 2048
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="g"
/db_xref="dbSNP:1950702946"
variation 2049..2053
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="ccccc"
/replace="ccccccc"
/db_xref="dbSNP:1950702782"
variation 2050
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1950702902"
variation 2051
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1950702832"
variation 2054
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:925838751"
variation 2057
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1361292300"
variation 2059
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1593437462"
variation 2063
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:974644686"
variation 2065..2069
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="acgca"
/db_xref="dbSNP:1950702436"
variation 2066
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:567430632"
variation 2067
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1341331550"
variation 2071
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:911586191"
variation 2074
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:542153503"
variation 2077
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1156419163"
variation 2078
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1435059615"
variation 2079
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1593437426"
variation 2081
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:370209943"
variation 2083
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:950536054"
variation 2084
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950702021"
variation 2088
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:559705268"
variation 2090
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1010901456"
variation 2093
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950701848"
variation 2094
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1298882440"
variation 2096
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:893810615"
variation 2102
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:963549804"
variation 2110..2111
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="ct"
/replace="ctct"
/db_xref="dbSNP:2136907189"
variation 2111..2113
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="t"
/replace="ttt"
/replace="ttttt"
/db_xref="dbSNP:3832804"
variation 2111
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="t"
/replace="tgt"
/db_xref="dbSNP:2136907182"
variation 2112
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="t"
/replace="tat"
/db_xref="dbSNP:2136907172"
variation 2114
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1593437365"
variation 2115
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:111820152"
variation 2116
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1052601435"
variation 2117
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950701329"
variation 2118
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1414983132"
variation 2119
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950701238"
variation 2120
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="t"
/replace="tt"
/db_xref="dbSNP:1950701181"
variation 2124
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:935595520"
variation 2125..2128
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="gaga"
/replace="gagaga"
/db_xref="dbSNP:1950701113"
variation 2129..2131
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="cc"
/replace="ccc"
/db_xref="dbSNP:1418783722"
variation 2134
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950701021"
variation 2135
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1002477975"
variation 2142
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1278595598"
variation 2144
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1347878070"
variation 2145..2149
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="gggg"
/replace="ggggg"
/db_xref="dbSNP:1950700679"
variation 2145
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:541179525"
variation 2146
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1950700733"
variation 2149
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:576945941"
variation 2151
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:769326943"
variation 2152
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:892514179"
variation 2153
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1054288089"
variation 2158
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:367620504"
variation 2159
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:916367947"
variation 2162
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:973064787"
variation 2168
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1038910312"
variation 2169
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:963001005"
variation 2170..2171
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="cc"
/replace="ga"
/db_xref="dbSNP:796574941"
variation 2170
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950700117"
variation 2171
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:943323229"
variation 2173
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950699977"
variation 2174
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950699935"
variation 2178
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950699905"
variation 2181
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1950699872"
variation 2184
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:370314942"
variation 2185
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950699794"
variation 2186
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950699755"
variation 2187
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:182916402"
variation 2188
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:3741490"
variation 2193
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1443374356"
variation 2195
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950699663"
variation 2197
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2136906865"
variation 2199
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:983339952"
variation 2202
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:1950699592"
variation 2204
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1301770978"
variation 2210
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:987116079"
variation 2211
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950699497"
variation 2213
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:554895850"
variation 2215
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2136906816"
variation 2216
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950699427"
variation 2220
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1950699392"
variation 2225
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1298316988"
variation 2228
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950699320"
variation 2230
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:75237791"
variation 2231
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:746850522"
variation 2233
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1353265460"
variation 2234
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:777597930"
variation 2235
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:973165920"
variation 2239
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:758214417"
variation 2240
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:996057076"
variation 2242
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:192844482"
variation 2243..2247
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="gag"
/replace="gagag"
/db_xref="dbSNP:1423726431"
variation 2243
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:547619077"
variation 2249
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:2136906701"
variation 2251
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1010952147"
variation 2252
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1002451487"
variation 2255
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950698849"
variation 2258
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:893777773"
variation 2262
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1030977492"
variation 2264
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1163686844"
variation 2274
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950698740"
variation 2275
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1950698712"
variation 2276
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:781543889"
variation 2277
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:906815915"
variation 2278
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:2136906626"
variation 2281
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1415593537"
variation 2283
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1046993159"
variation 2293
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1334852400"
variation 2294
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:3741489"
variation 2300
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950698472"
variation 2303
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950698451"
variation 2304
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1270832087"
variation 2305
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1450666893"
variation 2307
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:4758909"
variation 2315
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1201112509"
variation 2318
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1192780707"
variation 2325
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1950698208"
variation 2329
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1258321216"
variation 2333
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:112870346"
variation 2335
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1593437106"
variation 2338
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1476204979"
variation 2339
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1163079471"
variation 2341
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1593437086"
variation 2344
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:754605513"
variation 2345
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:549889950"
variation 2348
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1458219528"
variation 2355
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1413405596"
variation 2356..2360
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="ag"
/replace="aggag"
/db_xref="dbSNP:1950697843"
variation 2363
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1037421988"
variation 2365..2367
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="gag"
/db_xref="dbSNP:1272645289"
variation 2365
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950697778"
variation 2369
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1053774837"
variation 2374
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1401470577"
variation 2378
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950697578"
variation 2379
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1231595234"
variation 2382
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1161815482"
variation 2387
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1950697422"
variation 2388
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1343788492"
variation 2389
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1593437040"
variation 2390
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:941773272"
variation 2391
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:907515157"
variation 2392
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:142376269"
variation 2395
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950697143"
variation 2397..2398
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="aa"
/replace="aaa"
/db_xref="dbSNP:36039891"
variation 2397
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950697092"
variation 2401
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950696998"
variation 2405
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1950696954"
variation 2408
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:933225060"
variation 2418
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1355291257"
variation 2420
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1223981564"
variation 2430
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:923251377"
variation 2431
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:1950696730"
variation 2432
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1950696680"
variation 2434
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:755120503"
variation 2435
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:2136906288"
variation 2437
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950696585"
variation 2438
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1566171220"
variation 2442
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:964542689"
variation 2446
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:1021425081"
variation 2452..2454
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="tt"
/replace="ttt"
/db_xref="dbSNP:1950696422"
variation 2452
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950696455"
variation 2459..2466
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="ctt"
/replace="cttatctt"
/db_xref="dbSNP:943198387"
variation 2459
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1950696399"
variation 2464
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:989498094"
variation 2469
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1215845332"
variation 2479
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950696268"
variation 2481
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1258077252"
variation 2482
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950696224"
variation 2483
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950696187"
variation 2485
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950696162"
variation 2487
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1296311836"
variation 2489
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2136906187"
variation 2493
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:958138392"
variation 2496
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950696070"
variation 2501..2507
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="aata"
/replace="aataata"
/db_xref="dbSNP:1950695982"
variation 2502..2511
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="ataat"
/replace="ataatataat"
/db_xref="dbSNP:1950695893"
variation 2504
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:1950696039"
variation 2506..2521
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="tataattta"
/replace="tataatttataattta"
/db_xref="dbSNP:1401013436"
variation 2506
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1486597998"
variation 2509
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950695953"
variation 2510
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:1593436977"
variation 2514
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950695859"
variation 2517
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1950695816"
variation 2518
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1030946220"
variation 2522
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950695735"
variation 2526
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1236969685"
variation 2529
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1950695685"
variation 2531
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:911779056"
variation 2532..2533
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="t"
/db_xref="dbSNP:1950695597"
variation 2532
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:1950695623"
variation 2533
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:1950695572"
variation 2534
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1179105860"
variation 2536
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1950695511"
variation 2538
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1406240647"
variation 2540
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:560709767"
variation 2541
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1950695431"
variation 2545
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:999568389"
variation 2547
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950695356"
variation 2549
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:548922117"
variation 2550
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1377843900"
variation 2551..2554
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="t"
/replace="tatt"
/db_xref="dbSNP:1950695202"
variation 2552
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:1950695263"
variation 2553
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950695232"
variation 2554..2557
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="ttga"
/db_xref="dbSNP:1950695140"
variation 2556
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1025188661"
variation 2557..2559
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="aa"
/replace="aaa"
/db_xref="dbSNP:1950695100"
variation 2565
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1331697816"
variation 2566
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:973134921"
variation 2567
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1012923039"
variation 2568
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:2136905955"
variation 2569
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950694997"
variation 2570
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:895287582"
variation 2572
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950694939"
variation 2573
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1950694917"
variation 2574
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2136905920"
variation 2575..2576
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="g"
/db_xref="dbSNP:34409499"
variation 2576
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1165063779"
variation 2581..2583
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="t"
/replace="tat"
/db_xref="dbSNP:1950694812"
variation 2582
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:2136905904"
variation 2583
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950694782"
variation 2585..2591
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="aaaaaaa"
/replace="aaaaaaaa"
/db_xref="dbSNP:1350044921"
variation 2585
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1374414628"
variation 2586
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:926776920"
variation 2591
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1280739400"
variation 2592
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1593436904"
variation 2595
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1593436894"
variation 2596
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:530330334"
variation 2597
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:971314022"
variation 2603
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1438398757"
variation 2604
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950694458"
variation 2618
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1950694435"
variation 2620
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1206923715"
variation 2621
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1231446323"
variation 2622
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1406251214"
variation 2624
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:941743070"
variation 2625
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950694296"
variation 2627
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:115799873"
variation 2628
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:541241838"
variation 2631
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950694155"
variation 2632
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:2136905761"
variation 2633
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950694126"
variation 2634
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950694099"
variation 2643
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1047424647"
variation 2645
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:932962176"
variation 2646
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:753996875"
variation 2647
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1211863620"
variation 2649
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950693980"
variation 2650
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1397721159"
variation 2651
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1489535422"
variation 2653
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1266210457"
variation 2656..2660
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="aaccg"
/db_xref="dbSNP:1950693729"
variation 2658..2659
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="atgctgctcccttgtgtgagtgaccacggccccgagcctggggctgga
cgcaggtcccagga"
/db_xref="dbSNP:1950693826"
variation 2658
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1316055975"
variation 2659..2660
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="acggccccgagcctggggctggacgcaggtcccaggacgtgct"
/db_xref="dbSNP:1441439409"
variation 2659
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:766575351"
variation 2660..2661
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="agcctggggctggacgcaggtcccaggacgtgctgctcccttct"
/replace="caggtcccaggacgtgctgctcccttct"
/replace="ctcccttct"
/replace="tgcattcccttct"
/replace="tgctgctcccttct"
/db_xref="dbSNP:rs1336309071"
variation 2661..2771
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="gtgagtgaccgcggccccgagcctggggctggacgcaggtcccaggac
"
/replace="gtgagtgaccgcggccccgagcctggggctggacgcaggtcccaggac
atgctgctcccttgtgtgagtgaccgcggccccgagcctggggctggacgcaggtccc
aggac"
/db_xref="dbSNP:1950691745"
variation 2661
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950693572"
variation 2661
/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 2662
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:974656529"
variation 2663
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1304579464"
variation 2666
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:1593436768"
variation 2668
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1593436758"
variation 2670
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:577007021"
variation 2671
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:60054929"
variation 2672..2708
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="cggccccgagcctggggctggacgcaggtcccaggac"
/replace="cggccccgagcctggggctggacgcaggtcccaggacgtgctgctccc
ttctgtgagtgaccacggccccgagcctggggctggacgcaggtcccaggac"
/db_xref="dbSNP:1566170955"
variation 2672
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:137860747"
variation 2673
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:543507917"
variation 2674
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1339972650"
variation 2676
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1950693259"
variation 2678
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:576425597"
variation 2679
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:978587251"
variation 2682..2683
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="cc"
/db_xref="dbSNP:1950693096"
variation 2682
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:970720837"
variation 2683
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950693066"
variation 2691
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1000902244"
variation 2694
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1025409954"
variation 2695
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1012477120"
variation 2696
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="cc"
/db_xref="dbSNP:1722609409"
variation 2701
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950692922"
variation 2702
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1452627569"
variation 2703
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1950692858"
variation 2705
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:899887350"
variation 2708
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950692769"
variation 2709
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:373137192"
variation 2710..2796
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="tgctgctcccttgtgtgagtgacc"
/replace="tgctgctcccttgtgtgagtgaccgcggccccgagcctggggctggac
gcaggtcccaggacgtgctgctcccttgtgtgagtgacc"
/db_xref="dbSNP:1950691334"
variation 2712
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:554677515"
variation 2715
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:377537751"
variation 2719
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1420814830"
variation 2721..2722
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="ac"
/db_xref="dbSNP:1950692612"
variation 2722
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:796139459"
variation 2723
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1006432643"
variation 2729
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1950692520"
variation 2732
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1396446600"
variation 2733..2734
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="acggccccgagcctggggctggacgcaggtcccaggacgtgctgctcc
cttctgtgagt"
/replace="acggccccgagcctggggctggacgcaggtcccaggacgtgctgctcc
cttctgtgagtgaccacggccccgagcctggggctggacgcaggtcccaggacatgct
gctcccttctgtgagt"
/replace="acggccccgagcctggggctggacgcaggtcccaggacgtgctgctcc
cttgtgtgagt"
/db_xref="dbSNP:1566170899"
variation 2733
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1384812230"
variation 2734..2735
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="acca"
/db_xref="dbSNP:1566170888"
variation 2734
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:15638"
variation 2735
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:111799372"
variation 2736
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:572274927"
variation 2738
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950692211"
variation 2739
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:997687935"
variation 2741
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:376925671"
variation 2742
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1039131607"
variation 2746
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950692083"
variation 2747..2797
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="tggggctggacgcaggtcccaggacgtgctgctcccttgtgtgagtga
cca"
/db_xref="dbSNP:1566170810"
variation 2747
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:373528706"
variation 2748
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1593436635"
variation 2752
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1354479573"
variation 2753
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="t"
/replace="tt"
/db_xref="dbSNP:1192334475"
variation 2757
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:369891917"
variation 2758
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1950691911"
variation 2759
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1950691881"
variation 2761
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1950691853"
variation 2762
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:867795922"
variation 2769
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:187667016"
variation 2771
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1186063298"
variation 2772
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:111786421"
variation 2773..2784
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="tgctgctccctt"
/replace="tgctgctcccttctgtgagtgaccacggccccgagcctggggctggac
gcaggtcccaggacatgctgctccctt"
/db_xref="dbSNP:1950691518"
variation 2773
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950691632"
variation 2775..2776
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="a"
/db_xref="dbSNP:1950691609"
variation 2777..2778
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="gc"
/db_xref="dbSNP:1950691577"
variation 2780
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1485012640"
variation 2784
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1054216011"
variation 2785
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:75167846"
variation 2788
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950691423"
variation 2789
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950691387"
variation 2792
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950691364"
variation 2797
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1456063340"
variation 2798
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:538873969"
variation 2799
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:117246365"
variation 2800..2812
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="gccccaagcccag"
/db_xref="dbSNP:1230976787"
variation 2800
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1566170789"
variation 2801
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950691154"
variation 2802
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950691128"
variation 2803
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1007364269"
variation 2804
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1218487646"
variation 2805
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:111338463"
variation 2806
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950690986"
variation 2810
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:978174785"
variation 2811
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:8021"
variation 2813
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:917908364"
variation 2818
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950690803"
variation 2820
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1332266605"
variation 2821
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:890301777"
variation 2822
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1301350623"
variation 2826
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1593436516"
variation 2828
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950690645"
variation 2831
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1950690593"
variation 2832
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1051667411"
variation 2833
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950690530"
variation 2834
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:991258229"
variation 2835
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:959608059"
variation 2836
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1016485269"
variation 2837
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1006486333"
variation 2839
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:73489148"
variation 2840
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950690229"
variation 2843
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1950690169"
variation 2844
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1364197764"
variation 2845
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1455110594"
variation 2853
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1026915435"
variation 2855
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1359866417"
variation 2856
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1566170710"
variation 2857
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1172254217"
variation 2858
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1468017193"
variation 2859
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1950689734"
variation 2860
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1376990440"
variation 2865
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950689662"
variation 2866
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:997254637"
variation 2869
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1395673079"
variation 2870
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1378783852"
variation 2875
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="cggtc"
/db_xref="dbSNP:1950689542"
variation 2878
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950689502"
variation 2879
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:941680964"
variation 2880
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="a"
/db_xref="dbSNP:2136904893"
variation 2882
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:535014873"
variation 2885
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1950689402"
variation 2890
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1950689380"
variation 2891
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950689346"
variation 2898..2910
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="tg"
/replace="tggcttccgcctg"
/db_xref="dbSNP:1950689207"
variation 2898
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:1238486499"
variation 2905
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1038687461"
variation 2906
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1007221366"
variation 2907
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:182104463"
variation 2910
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:980532486"
variation 2911
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1349314061"
variation 2913
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950689114"
variation 2915
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1213577280"
variation 2921
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1436173408"
variation 2923
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950689033"
variation 2924
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:764304023"
variation 2929
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2136904817"
variation 2932
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:566065778"
variation 2936
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1481966746"
variation 2939
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1950688911"
variation 2942
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2136904799"
variation 2943
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950688886"
variation 2947
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1950688853"
variation 2950
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1199546557"
variation 2953
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1950688798"
variation 2954
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:892808322"
variation 2955..2959
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="ttttt"
/replace="tttttt"
/db_xref="dbSNP:1950688694"
variation 2958
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:949556782"
variation 2960..2961
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="gg"
/db_xref="dbSNP:1176616028"
variation 2962..2969
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="aaaa"
/replace="aaaaaa"
/replace="aaaaaaa"
/replace="aaaaaaaa"
/replace="aaaaaaaaa"
/db_xref="dbSNP:rs957212862"
variation 2962
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1265543823"
variation 2963
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1054268966"
variation 2964
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:934594162"
variation 2965
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1488453973"
variation 2970
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:191072646"
variation 2971..2976
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="ttttt"
/replace="tttttt"
/replace="ttttttt"
/db_xref="dbSNP:1566170618"
variation 2973
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1256563011"
variation 2975..2981
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="tt"
/replace="ttatctt"
/db_xref="dbSNP:1950688278"
variation 2977
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:566122046"
variation 2980
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:949484292"
variation 2981
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1950688259"
variation 2982
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950688232"
variation 2994
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950688210"
variation 2995
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1018288530"
variation 2996
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1950688147"
variation 2997
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950688117"
variation 3002
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1299758456"
variation 3003
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:549120489"
variation 3011
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950688014"
variation 3016
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:918030300"
variation 3018
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:565128269"
variation 3022
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1458856890"
variation 3030..3037
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="cttct"
/replace="cttcttct"
/db_xref="dbSNP:1468716986"
variation 3031
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:937960418"
variation 3032
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:909224402"
variation 3033
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1226033314"
variation 3036
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1046106"
variation 3038
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950687714"
variation 3043
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1315555821"
variation 3044
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950687665"
variation 3045
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1279655347"
variation 3046
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1950687603"
variation 3047
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:985017981"
variation 3048
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1950687569"
variation 3055
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:1950687539"
variation 3056
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1432491382"
variation 3059
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:753726528"
variation 3061
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1950687442"
variation 3069
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1425798710"
variation 3071
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2136904528"
variation 3075
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950687386"
variation 3077
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:529547282"
variation 3080..3097
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="ctg"
/replace="ctgagaagcagcaatctg"
/db_xref="dbSNP:1950687169"
variation 3080
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:148270257"
variation 3082
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:11542904"
variation 3093
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:2136904496"
variation 3095
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:976689419"
variation 3096
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950687203"
variation 3097
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:2136904480"
variation 3098
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950687133"
variation 3099
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1950687101"
variation 3103
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:965819930"
variation 3105
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1950687045"
variation 3113
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="g"
/db_xref="dbSNP:897708347"
variation 3113
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1367604138"
variation 3116
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1037632913"
variation 3118
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950686909"
variation 3120
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950686881"
variation 3121
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950686849"
variation 3131
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:941651179"
variation 3132
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1046130"
regulatory 3134..3139
/regulatory_class="polyA_signal_sequence"
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
variation 3134
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1950686736"
variation 3135
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950686709"
variation 3140
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:904877930"
variation 3141
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1017734390"
variation 3145
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:376262240"
variation 3146
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1007273719"
variation 3147
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:892777244"
variation 3148
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:561407931"
variation 3152
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1244757352"
variation 3154
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1298125618"
variation 3155
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:998710936"
variation 3157
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950686377"
polyA_site 3158
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
ORIGIN
agctgagggagccgcaatgtctcttgacagcggcggcggcgcagccggttccgggttcggcgcggggcggggatgtgaatcccgatggagcggcccgaggaaggcaagcagtcgccgccgccgcagccctggggacggctcctgcgtctgggcgcggaggagggcgagccgcacgtcctcctgaggaagcgggagtggaccatcgggcggagacgaggttgcgacctttccttccccagcaataaactggtctctggagatcactgtagaattgtagtggatgaaaaatcaggtcaggtgacactggaagataccagcaccagtggaacagtgattaacaagctgaaggttgttaagaagcagacatgccctttacagactggggatgtcatctacttggtgtacaggaagaatgaaccggaacacaacgtggcatacctctatgaatctttaagtgaaaagcaaggcatgacacaagaatcctttgagatggtgccttgctgtgttgcccaggctggtctaaaactcctgggatcaagtgatcctcccaccttggcctcccaaagtattgtgattacagggtctgggggtggtggcatctcccctaaaggaagtggtccctctgtggcaagtgatgaagtctccagctttgcctcagctctcccagacagaaagactgcgtccttttcgtcgttggaaccccaggatcaggaggatttggagcccgtgaagaagaaaatgagaggagatggggaccttgacctgaacgggcagttgttggtcgcacaaccgcgtagaaatgcccaaaccgtccacgaggacgtcagagcagcggctgggaagccagacaagatggaggagacgctgacatgcatcatctgccaggacctgctgcacgactgcgtgagtttgcagccctgcatgcacacgttctgcgcggcttgctactcgggctggatggagcgctcgtccctgtgtcctacctgccgctgtcccgtggagcggatctgtaaaaaccacatcctcaacaacctcgtggaagcatacctcatccagcatccagacaagagtcgcagtgaagaagatgtgcaaagtatggatgccaggaataaaatcactcaagacatgctgcagcccaaagtcaggcggtctttttctgatgaagaagggagttcagaggacctgctggagctgtcagacgttgacagtgagtcctcagacattagccagccatacgtcgtgtgccggcagtgtcctgagtacagaaggcaggcggcgcagcctccccactgcccagcacccgagggcgagccaggagccccacaggccctgggggatgcaccctccacgtccgtcagcctgacgacagcagtccaggattacgtgtgccctctgcaaggaagccacgccctgtgcacctgctgcttccagcccatgcccgaccggagagcggagcgcgagcaggacccgcgtgtcgcccctcagcagtgtgcggtctgcctgcagcctttctgccacctgtactggggctgcacccggaccggctgctacggctgcctggccccgttttgtgagctcaacctgggtgacaagtgtctggacggcgtgctgaacaacaacagctacgagtcagacatcctgaagaattacctggcaaccagaggtttgacatggaaaaacatgttgaccgagagcctcgtggctctccagcggggagtgtttctgctgtctgattacagagtcacgggagacaccgttctgtgttactgctgtggcctgcgcagcttccgtgagctgacctatcagtatcggcagaacattcctgcttccgagttgccagtggccgtaacatcccgtcctgactgctactggggccgtaactgccgcactcaggtgaaagctcaccacgccatgaaattcaatcatatctgtgaacagacaaggttcaaaaactaagcatccagaggccctgagcagctttcagcactggaggtgaagagagcgtgtttttaaaatacagagacaagcacgtcaaggtgttttcacagccccctgagggaagggacgcagggtctccgacaggtgctctggggtgactcttctgtggagctttaccctctgagtgagaccctccccagagccccgggggccgcagcccgccctcctggtgagcgctgggcagggctcgtggtggcatcagcagcagagacgaagcctttctgtaacatgcggccgtcccgccgagaggggcagttttgctcttttgtacattttccgaaactacagttaaagcagaagtctgtttttaggaaaagtttcaagggagaagggcaagtttatcaaaaacattgtttcaggagaagggagcataagtttacagcctacaggacgtacacaatatcctgctgctgggaaaaccacagcattttatctattttttattttaataggtttggtgcttatcttctaataagatttaaatgtcacaaactgtagcacaaataatataatttataatttacaaattgactaaaattgggtatagtatggtatttgaaagaataagcatatgcttctgtttattaaaaaaagaaaccttccaatgtccaaaactgctaaccctcgacgtggccgccaagttagtcgctccttgctaaccggtgagtgaccgcggccccgagcctggggctggacgcaggtcccaggacatgctgctcccttgtgtgagtgaccgcggccccgagcctggggctggacgcaggtcccaggacgtgctgctcccttgtgtgagtgaccacggccccaagcccagggctggaggcaggtcccaggacgcgccgctccctcatgctgcccgggcccttcctccaagaccctacagagcctgaggggcaccttggcttccgcctgtgctagctttgccatgtcatctggaataatacttgaaattttgatttttggaaaaaaaagttttttatcttttgttgaaatcacctgttatccttgtttgtaaactgataacttttttgcttcttctcaggaatacagttttcaactgttgtcttgctcttgatagaaactgagaagcagcaatctgtatttgtggaggaaagtcctctcttttgcatattctaataaatgagccgcgtttgctcctcaaaaaaaaaa
//
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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