ver.2
Home
|
Help
|
Advanced search
Previous release (v1)
2024-04-19 19:37:45, GGRNA.v2 : RefSeq release 222 (Jan, 2024)
LOCUS NM_001161347 3015 bp mRNA linear PRI 17-APR-2023
DEFINITION Homo sapiens checkpoint with forkhead and ring finger domains
(CHFR), transcript variant 5, mRNA.
ACCESSION NM_001161347
VERSION NM_001161347.1
KEYWORDS RefSeq.
SOURCE Homo sapiens (human)
ORGANISM Homo sapiens
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi;
Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini;
Catarrhini; Hominidae; Homo.
REFERENCE 1 (bases 1 to 3015)
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 3015)
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 3015)
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 3015)
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 3015)
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 3015)
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 3015)
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 3015)
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 3015)
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 3015)
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, AK302785.1,
AK027687.1, AC127070.10 and BC012072.1.
Summary: This gene encodes an E3 ubiquitin-protein ligase required
for the maintenance of the antephase checkpoint that regulates cell
cycle entry into mitosis and, therefore, may play a key role in
cell cycle progression and tumorigenesis. The encoded protein has
an N-terminal forkhead-associated domain, a central RING-finger
domain, and a cysteine-rich C-terminal region. Alternatively
spliced transcript variants that encode different protein isoforms
have been described. [provided by RefSeq, Mar 2014].
Sequence Note: This RefSeq record was created from transcript and
genomic sequence data to make the sequence consistent with the
reference genome assembly. The genomic coordinates used for the
transcript record were based on transcript alignments.
Publication Note: This RefSeq record includes a subset of the
publications that are available for this gene. Please see the Gene
record to access additional publications.
##Evidence-Data-START##
Transcript exon combination :: AK302785.1 [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
1-15 BP313700.1 1-15
16-1545 AK302785.1 1-1530
1546-1546 AK027687.1 1780-1780
1547-1842 AK302785.1 1532-1827
1843-2658 AC127070.10 108304-109119
2659-3015 BC012072.1 2825-3181
FEATURES Location/Qualifiers
source 1..3015
/organism="Homo sapiens"
/mol_type="mRNA"
/db_xref="taxon:9606"
/chromosome="12"
/map="12q24.33"
gene 1..3015
/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..1803
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/EC_number="2.3.2.27"
/note="isoform 5 is encoded by transcript variant 5; 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 5"
/protein_id="NP_001154819.1"
/db_xref="CCDS:CCDS53847.1"
/db_xref="GeneID:55743"
/db_xref="HGNC:HGNC:20455"
/db_xref="MIM:605209"
/translation="
MERPEEGKQSPPPQPWGRLLRLGAEEGEPHVLLRKREWTIGRRRGCDLSFPSNKLVSGDHCRIVVDEKSGQVTLEDTSTSGTVINKLKVVKKQTCPLQTGDVIYLVYRKNEPEHRSGGGGISPKGSGPSVASDEVSSFASALPDRKTASFSSLEPQDQEDLEPVKKKMRGDGDLDLNGQLLVAQPRRNAQTVHEDVRAAAGKPDKMEETLTCIICQDLLHDCVSLQPCMHTFCAACYSGWMERSSLCPTCRCPVERICKNHILNNLVEAYLIQHPDKSRSEEDVQSMDARNKITQDMLQPKVRRSFSDEEGSSEDLLELSDVDSESSDISQPYVVCRQCPEYRRQAAQPPHCPAPEGEPGAPQALGDAPSTSVSLTTAVQDYVCPLQGSHALCTCCFQPMPDRRAEREQDPRVAPQQCAVCLQPFCHLYWGCTRTGCYGCLAPFCELNLGDKCLDGVLNNNSYESDILKNYLATRGLTWKNMLTESLVALQRGVFLLSDYRVTGDTVLCYCCGLRSFRELTYQYRQNIPASELPVAVTSRPDCYWGRNCRTQVKAHHAMKFNHICEQTRFKN"
misc_feature 127..426
/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)
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/note="homodimer interface [polypeptide binding]; other
site"
/db_xref="CDD:438724"
misc_feature 175..>696
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/note="type VI secretion system FHA domain protein;
Region: VI_FHA; TIGR03354"
/db_xref="CDD:274537"
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 700..>1314
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/note="DNA repair protein rad18; Region: rad18; TIGR00599"
/db_xref="CDD:273165"
misc_feature 706..867
/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 1198..1668
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/note="Cysteine rich domain with multizinc binding
regions; Region: zf-CRD; pfam17979"
/db_xref="CDD:436187"
misc_feature 1702..1773
/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..595
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/inference="alignment:Splign:2.1.0"
variation 431
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1038150337"
variation 433
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:370517411"
variation 434
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1951211639"
variation 436
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1438318944"
variation 437
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:777186106"
variation 439..440
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="gg"
/db_xref="dbSNP:1189456093"
variation 439
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:766667278"
variation 442
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:761034338"
variation 443
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1593482765"
variation 445
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:138637226"
variation 447
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1951211154"
variation 448
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1387477118"
variation 451
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:34220055"
variation 452
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:761525824"
variation 453
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2136982888"
variation 458
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1951210868"
variation 461
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:774070010"
variation 462
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:1419993206"
variation 463
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1951210693"
variation 464
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:201192149"
variation 465
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:989203291"
variation 467
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1951210512"
variation 471
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:796201985"
variation 472
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1163339779"
variation 480
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:749192848"
variation 484
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:374107669"
variation 486
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:769505625"
variation 491
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:780945230"
variation 495
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1951210091"
variation 504
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1951210040"
variation 508
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:35206714"
variation 510
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1951209926"
variation 511
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1366834805"
variation 513
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1038008124"
variation 515
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:560433355"
variation 517..523
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="aga"
/replace="agaaaga"
/db_xref="dbSNP:1951209560"
variation 520
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:201727566"
variation 524
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:2136982730"
variation 525
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:758662673"
variation 526
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:533118486"
variation 527
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:150995074"
variation 528
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:755027328"
variation 529..533
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="t"
/replace="tcctt"
/db_xref="dbSNP:2136982677"
variation 531
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:908433616"
variation 534
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:200213031"
variation 536
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:754307363"
variation 537
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:145246258"
variation 539
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:141183005"
variation 540
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:767988129"
variation 541..542
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="t"
/replace="tt"
/db_xref="dbSNP:766718829"
variation 543
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1566189184"
variation 544
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1423637297"
variation 547..550
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="ccc"
/replace="cccc"
/db_xref="dbSNP:762524769"
variation 547
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:751592981"
variation 549
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1951208832"
variation 551
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:373754363"
variation 552
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:761615752"
variation 553
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:147803776"
variation 555
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1566189143"
variation 557
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1951208615"
variation 561
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:774088595"
variation 562
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1472958431"
variation 570
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:768052255"
variation 571..573
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="cc"
/replace="ccc"
/db_xref="dbSNP:2136982524"
variation 572
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:762481129"
variation 573
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1025589682"
variation 574
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:775309126"
variation 576
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:764279540"
variation 577
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1951208249"
variation 578
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1463671908"
variation 580
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:974854406"
variation 583
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:1221100387"
variation 584
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1951208117"
variation 585
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:1238379063"
variation 586
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1951208036"
variation 587
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1566189061"
variation 592
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:745763828"
exon 596..755
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/inference="alignment:Splign:2.1.0"
variation 596
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1951157533"
variation 597
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:756088633"
variation 600
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1951157390"
variation 601
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:563202190"
variation 604
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2136974267"
variation 605
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1360404336"
variation 608
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1951157150"
variation 609
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:781748631"
variation 612
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:757715316"
variation 614
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:752016583"
variation 615
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:377318460"
variation 616
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:115096950"
variation 617
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1593477819"
variation 618
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1393923793"
variation 619..620
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="t"
/db_xref="dbSNP:776753889"
variation 620
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:1311480210"
variation 621
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:758139441"
variation 622
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:973250523"
variation 624
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1021390710"
variation 628
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:752281100"
variation 630
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:115431373"
variation 631
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:148618944"
variation 633
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:369526598"
variation 636
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:769878915"
variation 637
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:540759128"
variation 638
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:760584451"
variation 639
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:773102049"
variation 640
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:749537035"
variation 641
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:375174098"
variation 643
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:770024903"
variation 646
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1951155348"
variation 649
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:188170704"
variation 650
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:745889598"
variation 651
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1951155139"
variation 652
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:781395404"
variation 654
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:757876886"
variation 655
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1593477690"
variation 656
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1951154950"
variation 657
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:747517165"
variation 658
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:199761208"
variation 661
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1951154859"
variation 663
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1380131918"
variation 664
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:144838296"
variation 666
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1449844658"
variation 668
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1000960906"
variation 669
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:371434249"
variation 670
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:764757412"
variation 671
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="t"
/db_xref="dbSNP:768680290"
variation 671
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1464052810"
variation 673
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:754506935"
variation 674
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:149862277"
variation 677
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2136973920"
variation 678
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:765845584"
variation 680
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1277312621"
variation 681
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:746414469"
variation 682
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1341883561"
variation 683
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:2136973888"
variation 684
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1295926976"
variation 686
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1306779303"
variation 688
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1593477559"
variation 689
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1375950961"
variation 692
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2136973857"
variation 693
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:35011845"
variation 694
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1341253353"
variation 696
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1951153923"
variation 699
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1312306793"
variation 700
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:767348322"
variation 702
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1352413194"
variation 705
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2136973793"
variation 708
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:2136973786"
variation 710
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:761474515"
variation 711
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:775799321"
variation 712
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2136973760"
variation 714
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1951153687"
variation 715
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1951153632"
variation 717
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1369689338"
variation 719
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2136973741"
variation 721
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1951153534"
variation 723
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:770185579"
variation 724
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1252007101"
variation 726
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:12315353"
variation 729
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:146107503"
variation 735
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1368629651"
variation 738
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1186411942"
variation 739
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1951153233"
variation 740
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:759798633"
variation 741
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:2136973671"
variation 742
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1951153155"
variation 744
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1253421391"
variation 745
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1951153058"
variation 750
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:776915637"
variation 751
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:771123706"
variation 753
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1469130916"
exon 756..910
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/inference="alignment:Splign:2.1.0"
variation 756
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:560066373"
variation 760
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1213141444"
variation 764
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:780721649"
variation 765
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:565644778"
variation 769
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:987211916"
variation 772
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1566185781"
variation 773
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1174814592"
variation 774
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1478670195"
variation 776
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:751498855"
variation 777
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:142975525"
variation 780
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1466544467"
variation 783
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:138280939"
variation 784
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:754144763"
variation 785
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:921635691"
variation 786
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:766660009"
variation 787
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:760933260"
variation 788
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1221124973"
variation 794
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:368405665"
variation 795
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:767634272"
variation 797
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:762287710"
variation 798
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1367099211"
variation 800
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:774770261"
variation 801
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1951109519"
variation 805
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1433978124"
variation 807
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:553735979"
variation 808..810
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="gag"
/replace="gagag"
/db_xref="dbSNP:1566185670"
variation 809
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:968563777"
variation 811
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:749601873"
variation 812
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:775805064"
variation 815
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1402056016"
variation 816
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:769371058"
variation 817
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1593473549"
variation 819
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:745529097"
variation 820..821
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="ct"
/db_xref="dbSNP:1951108714"
variation 823
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1951108652"
variation 825
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:780623191"
variation 829
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:535313174"
variation 830
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:756736276"
variation 832
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1474574138"
variation 835
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:770034782"
variation 836
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:146343801"
variation 839
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1441931198"
variation 841
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:571101753"
variation 843
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:115029653"
variation 844
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1344021759"
variation 850
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:182092641"
variation 851
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:756361707"
variation 855
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1359376881"
variation 857
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:141404869"
variation 859
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1951107709"
variation 860
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:767497782"
variation 862
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1313496770"
variation 863
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1319716667"
variation 864
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1339366523"
variation 866
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1951107360"
variation 867
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1951107293"
variation 870
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:375199215"
variation 875
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:774858017"
variation 876
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1951107092"
variation 877
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1371529354"
variation 878
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:764629991"
variation 880
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1255988921"
variation 882
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:191062458"
variation 883
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:775898959"
variation 886
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1182669640"
variation 889
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1213131732"
variation 890
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1241168194"
variation 893
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1593473382"
variation 894
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:148311652"
variation 897
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:143181439"
variation 898
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1241159400"
variation 899
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1593473335"
variation 900
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:770380694"
variation 904
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:746470663"
variation 905
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:370386571"
variation 906
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2136966487"
variation 908
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1951106171"
exon 911..1073
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/inference="alignment:Splign:2.1.0"
variation 912
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1227736511"
variation 913..914
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="aa"
/db_xref="dbSNP:777961507"
variation 919
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1210874026"
variation 921
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:928539042"
variation 925..932
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="gaaga"
/replace="gaagaaga"
/db_xref="dbSNP:1951075030"
variation 925
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1951075098"
variation 927
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1566184554"
variation 934
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:879123151"
variation 936
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1229649968"
variation 938
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:777930523"
variation 939
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1566184534"
variation 941
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1293723698"
variation 943
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:377225060"
variation 947
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:748309050"
variation 948
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:778828908"
variation 949
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1434082116"
variation 950
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:200764395"
variation 951
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:369063253"
variation 952
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:1026572995"
variation 953
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:766865645"
variation 954
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:2062163"
variation 962
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1047280041"
variation 963
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:750119581"
variation 965
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:760238279"
variation 967
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:761337268"
variation 973
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:150467142"
variation 981
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:763498728"
variation 985
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1951074170"
variation 990
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:930183182"
variation 991
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1322357484"
variation 992
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:762961678"
variation 993
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:879252133"
variation 994
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:920205326"
variation 995
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:201828860"
variation 997
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1593470536"
variation 998
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:769607729"
variation 999
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:745615761"
variation 1002
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:776390811"
variation 1006
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:974463026"
variation 1009..1015
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="gaag"
/replace="gaagaag"
/db_xref="dbSNP:1434190222"
variation 1016
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:772321674"
variation 1019
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1315657949"
variation 1022
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="cc"
/db_xref="dbSNP:1951073572"
variation 1022
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1413044699"
variation 1026
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1353432969"
variation 1030
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1951073448"
variation 1033
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1309789349"
variation 1038
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:748314312"
variation 1044
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1283784330"
variation 1045
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1951073286"
variation 1047
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1395585538"
variation 1048
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1165776578"
variation 1054
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1951073172"
variation 1056
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1951073138"
variation 1058
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:779111370"
variation 1059
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1951073053"
variation 1062
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1368718436"
variation 1064
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1951072973"
variation 1071
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:754958760"
exon 1074..1216
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/inference="alignment:Splign:2.1.0"
variation 1077
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1286314037"
variation 1078
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1020597739"
variation 1080
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:748419509"
variation 1081
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:372270460"
variation 1082
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1013270057"
variation 1083
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1438322046"
variation 1084
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:768814594"
variation 1085
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1318363216"
variation 1086
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:749373830"
variation 1087
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:150627547"
variation 1089
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:368755833"
variation 1093
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1435723841"
variation 1094
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:746360566"
variation 1095
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1191956640"
variation 1101
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1451601823"
variation 1103
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:781699438"
variation 1106
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:757496767"
variation 1110
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1192492326"
variation 1112
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950995102"
variation 1114
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1445358565"
variation 1115
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950994995"
variation 1121
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:374229656"
variation 1122
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:777240371"
variation 1123
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1303770543"
variation 1124
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:371541325"
variation 1125
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:563852229"
variation 1129
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1231849613"
variation 1130
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1950994654"
variation 1132
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1366854652"
variation 1133
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1270421677"
variation 1134
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1429332642"
variation 1136
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1176161885"
variation 1137
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:764723102"
variation 1143
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2136951422"
variation 1147
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1237028076"
variation 1149
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:759529335"
variation 1150
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:753721064"
variation 1152
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1375184437"
variation 1153
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950993996"
variation 1154
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:367968934"
variation 1155
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:374006779"
variation 1156
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:774658371"
variation 1157
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1167629443"
variation 1158
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1566181842"
variation 1159
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:924051400"
variation 1160
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1593463729"
variation 1161
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1041545091"
variation 1165
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:768798394"
variation 1167
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1239336733"
variation 1172
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950993248"
variation 1180
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950993189"
variation 1182
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1189940191"
variation 1185
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950993053"
variation 1187
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:138207644"
variation 1188
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1593463695"
variation 1189
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1256747525"
variation 1191
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1379314322"
variation 1192
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:775767314"
variation 1195
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1196421815"
variation 1196
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:769933100"
variation 1197
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:746380972"
variation 1198
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:1215461680"
variation 1200
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:781511228"
variation 1201
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:141835819"
variation 1205
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:747380214"
variation 1208
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:778169456"
variation 1210
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:1355326421"
variation 1211
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:752333209"
variation 1212
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:536396076"
exon 1217..1336
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/inference="alignment:Splign:2.1.0"
variation 1217
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1402157616"
variation 1218
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:757077660"
variation 1219
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1950950768"
variation 1221
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:146976267"
variation 1223
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:765605647"
variation 1224
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1408464611"
variation 1228
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2136945225"
variation 1230
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:141349945"
variation 1231
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:776642806"
variation 1235
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1593459784"
variation 1236
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1306934237"
variation 1237
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:764423128"
variation 1238
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1950950185"
variation 1240
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:766469365"
variation 1242
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:761102171"
variation 1243
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2136945164"
variation 1247
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1304421220"
variation 1251
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:773703522"
variation 1252
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:772460210"
variation 1254
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:147791929"
variation 1255
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1454391193"
variation 1259
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1345653105"
variation 1260
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:116286061"
variation 1263
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:768361418"
variation 1264
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1593459724"
variation 1265
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1396714833"
variation 1266..1273
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="ctgct"
/replace="ctgctgct"
/db_xref="dbSNP:1363396811"
variation 1266
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:748952886"
variation 1267
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:763257394"
variation 1269
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1278317795"
variation 1275
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1950949058"
variation 1276
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1593459675"
variation 1277
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:779441212"
variation 1278
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:775978433"
variation 1285
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1187706335"
variation 1287
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:781224248"
variation 1288
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:757239007"
variation 1289
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1593459653"
variation 1291
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:936864653"
variation 1292
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:969442993"
variation 1295
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:751440176"
variation 1297
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1950948312"
variation 1298
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2306541"
variation 1299
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:755310429"
variation 1300
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1298012137"
variation 1302
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950947947"
variation 1303
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:754035414"
variation 1304
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:944300584"
variation 1305
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:766376169"
variation 1306
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:150920425"
variation 1309
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1015010652"
variation 1310
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:773617183"
variation 1312
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950947517"
variation 1314
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2136944907"
variation 1316
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:768065335"
variation 1317
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:142511371"
variation 1318
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:114117795"
variation 1319..1322
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="gt"
/replace="gtgt"
/db_xref="dbSNP:1950947070"
variation 1319
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:201454195"
variation 1320
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1172173801"
variation 1321
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:200436687"
variation 1323
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:920038038"
variation 1324
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:746554223"
variation 1326
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:973207321"
variation 1330
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1486915053"
variation 1332
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1346472721"
variation 1333
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1258850426"
variation 1335
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:769207559"
exon 1337..1420
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/inference="alignment:Splign:2.1.0"
variation 1339
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:372012714"
variation 1340
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:201350082"
variation 1341
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:7975454"
variation 1344
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:375656978"
variation 1350
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1335016856"
variation 1352
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:201237898"
variation 1353
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1442703181"
variation 1354
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:765505226"
variation 1355
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1324580295"
variation 1359
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950877727"
variation 1361
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950877687"
variation 1362
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950877658"
variation 1364
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1403110794"
variation 1371
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:759242088"
variation 1373..1376
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="ggg"
/replace="gggg"
/db_xref="dbSNP:1950877531"
variation 1376
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:953787024"
variation 1380
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:546055046"
variation 1381
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1593453012"
variation 1382
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:766020195"
variation 1384
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:371092913"
variation 1385
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:146156998"
variation 1386
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1454840670"
variation 1387
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:979112170"
variation 1388
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1252629926"
variation 1389
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:772089817"
variation 1390
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1448818469"
variation 1392
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1593452935"
variation 1393
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1950876982"
variation 1395
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1249069969"
variation 1397
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:767140702"
variation 1398
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:765611625"
variation 1399
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1349644861"
variation 1404
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:189987561"
variation 1405
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1236250946"
variation 1407
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:966632867"
variation 1410
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950876673"
variation 1411
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1348083185"
variation 1412
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1302248351"
variation 1413
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1433674477"
variation 1416
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1327743680"
exon 1421..1491
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/inference="alignment:Splign:2.1.0"
variation 1422
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:777921940"
variation 1427
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1950866672"
variation 1428
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:200853567"
variation 1431
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:748721756"
variation 1432
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1179840200"
variation 1434
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950866525"
variation 1435
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950866486"
variation 1437
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1471040037"
variation 1438
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:1950866384"
variation 1440
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1415191475"
variation 1442
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1233090445"
variation 1449
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:372404283"
variation 1450
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:755522022"
variation 1451
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:754297675"
variation 1452
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1323808548"
variation 1459..1468
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="aacaaca"
/replace="aacaacaaca"
/db_xref="dbSNP:1950865942"
variation 1461
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1213796881"
variation 1462
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:780565079"
variation 1463
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1288355908"
variation 1466
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1225827826"
variation 1467
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:755891788"
variation 1469
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1288380542"
variation 1473
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:749973618"
variation 1474
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950865817"
variation 1475
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:1379904886"
variation 1476
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:767082498"
variation 1480
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1950865707"
variation 1481
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:1950865670"
variation 1482
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1416698488"
variation 1486
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:761176081"
variation 1491
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1326600805"
exon 1492..1579
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/inference="alignment:Splign:2.1.0"
variation 1493
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1432073088"
variation 1494
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950847784"
variation 1497
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1422500887"
variation 1498
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:899072283"
variation 1499
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1008556440"
variation 1502
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950847611"
variation 1504
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:776466473"
variation 1506
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1950847509"
variation 1508
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:576074865"
variation 1510..1521
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="gg"
/replace="ggtttgacatgg"
/db_xref="dbSNP:1950847213"
variation 1513
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:2306537"
variation 1518
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:536151635"
variation 1519
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1281285798"
variation 1520
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1378971375"
variation 1522..1526
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="aaaaa"
/replace="aaaaaa"
/db_xref="dbSNP:1224656808"
variation 1526
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1232869629"
variation 1528
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:200187965"
variation 1534
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:2136929281"
variation 1536
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:749821203"
variation 1537
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:780655269"
variation 1543
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:770399858"
variation 1545
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:899313894"
variation 1546
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2306536"
variation 1549
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1485801990"
variation 1550
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:781614371"
variation 1551
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:756917083"
variation 1554
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950846511"
variation 1556
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1313082363"
variation 1557
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1465200907"
variation 1558
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1357095646"
variation 1559
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:558156375"
variation 1566
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1363290036"
variation 1570
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="c"
/db_xref="dbSNP:1428595949"
variation 1577
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1423530802"
variation 1579
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1950846204"
exon 1580..1687
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/inference="alignment:Splign:2.1.0"
variation 1580
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1265969471"
variation 1584
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950758429"
variation 1585..1588
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="ag"
/replace="agag"
/db_xref="dbSNP:1950758380"
variation 1592
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:115684143"
variation 1593
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1222086097"
variation 1594
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950758289"
variation 1602
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:115566777"
variation 1603
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:758025460"
variation 1605
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:976650599"
variation 1606
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:747697880"
variation 1607
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:1566173893"
variation 1610
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1950757987"
variation 1613
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="aa"
/db_xref="dbSNP:2136917535"
variation 1613
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1356919481"
variation 1615
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:778392987"
variation 1616
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:754931883"
variation 1617
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1442480016"
variation 1626
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:937547511"
variation 1627
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:961309862"
variation 1628
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:557461509"
variation 1629
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1456695524"
variation 1631
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:766096241"
variation 1632
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:2136917474"
variation 1636
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:376798546"
variation 1637
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950757414"
variation 1641
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950757365"
variation 1642
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1439266364"
variation 1646
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:764448295"
variation 1647
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1950757240"
variation 1648
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1220708351"
variation 1650
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1195509679"
variation 1651
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:2136917397"
variation 1652
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:114483951"
variation 1653
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1950757063"
variation 1657
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:775769340"
variation 1658
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:144644143"
variation 1664
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950756927"
variation 1665
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1950756882"
variation 1677
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:373411620"
variation 1678
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:777155485"
variation 1684
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:76224039"
exon 1688..1760
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/inference="alignment:Splign:2.1.0"
variation 1692
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:772354359"
variation 1693
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:761464761"
variation 1694
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="t"
/replace="tt"
/db_xref="dbSNP:1476434657"
variation 1696
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1425682767"
variation 1699
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1593440414"
variation 1701
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1194364986"
variation 1707
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:774002945"
variation 1710
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1260717996"
variation 1711
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1212784968"
variation 1716
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:768078789"
variation 1717
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950735401"
variation 1723
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:192495200"
variation 1724
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:779420556"
variation 1727
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1950735266"
variation 1730..1734
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="gc"
/replace="gccgc"
/db_xref="dbSNP:1218603125"
variation 1732
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:769922499"
variation 1733
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:745735958"
variation 1736
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1339131647"
variation 1739
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:1188833829"
variation 1740
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950735030"
variation 1741
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1295444518"
variation 1743
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1449229353"
variation 1748
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1950734903"
variation 1749
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1340024053"
variation 1752
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950734826"
variation 1755
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:146332668"
variation 1756
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:371841032"
variation 1758
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1401175113"
variation 1759
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:752894210"
variation 1760
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:779235326"
exon 1761..3005
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/inference="alignment:Splign:2.1.0"
variation 1767
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1456116703"
variation 1769
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:549826875"
variation 1771
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1950704889"
variation 1772
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1223009144"
variation 1773
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:772496941"
variation 1776
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1950704757"
variation 1780
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1950704725"
variation 1781
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950704692"
variation 1786
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1288110354"
variation 1787
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1190631767"
variation 1791
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:200441646"
variation 1799
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2136907624"
variation 1803
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:1950704521"
variation 1804
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1242787279"
variation 1805
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950704441"
variation 1811
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:776670620"
variation 1812
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:770961851"
variation 1814
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1566171705"
variation 1815
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1238046110"
variation 1818
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:746869999"
variation 1819
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:777416500"
variation 1820
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:755292850"
variation 1821
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:973123804"
variation 1823
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:375664747"
variation 1826..1828
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="tt"
/replace="ttt"
/db_xref="dbSNP:1566171684"
variation 1829
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:780118329"
variation 1833
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1293032557"
variation 1834
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:756135373"
variation 1835..1836
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="tg"
/db_xref="dbSNP:1950704004"
variation 1840
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:750955936"
variation 1841
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1157735470"
variation 1842
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:531300162"
variation 1845
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:757695645"
variation 1846
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:113800546"
variation 1849
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:752032125"
variation 1850
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:549782692"
variation 1851
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:762683133"
variation 1868
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1314603974"
variation 1869
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950703637"
variation 1872..1873
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="aa"
/replace="aaa"
/db_xref="dbSNP:1950703539"
variation 1872
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:1353651008"
variation 1873
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1286369531"
variation 1874
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1045979"
variation 1877
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:954494653"
variation 1878
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:749186808"
variation 1880
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1283042988"
variation 1883
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1237120100"
variation 1884
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1348995249"
variation 1885
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2136907397"
variation 1886
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1593437486"
variation 1889
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1030178377"
variation 1894
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="a"
/db_xref="dbSNP:1950703000"
variation 1895
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="g"
/db_xref="dbSNP:1950702946"
variation 1896..1900
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="ccccc"
/replace="ccccccc"
/db_xref="dbSNP:1950702782"
variation 1897
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1950702902"
variation 1898
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1950702832"
variation 1901
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:925838751"
variation 1904
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1361292300"
variation 1906
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1593437462"
variation 1910
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:974644686"
variation 1912..1916
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="acgca"
/db_xref="dbSNP:1950702436"
variation 1913
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:567430632"
variation 1914
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1341331550"
variation 1918
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:911586191"
variation 1921
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:542153503"
variation 1924
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1156419163"
variation 1925
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1435059615"
variation 1926
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1593437426"
variation 1928
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:370209943"
variation 1930
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:950536054"
variation 1931
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950702021"
variation 1935
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:559705268"
variation 1937
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1010901456"
variation 1940
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950701848"
variation 1941
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1298882440"
variation 1943
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:893810615"
variation 1949
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:963549804"
variation 1957..1958
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="ct"
/replace="ctct"
/db_xref="dbSNP:2136907189"
variation 1958..1960
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="t"
/replace="ttt"
/replace="ttttt"
/db_xref="dbSNP:3832804"
variation 1958
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="t"
/replace="tgt"
/db_xref="dbSNP:2136907182"
variation 1959
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="t"
/replace="tat"
/db_xref="dbSNP:2136907172"
variation 1961
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1593437365"
variation 1962
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:111820152"
variation 1963
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1052601435"
variation 1964
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950701329"
variation 1965
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1414983132"
variation 1966
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950701238"
variation 1967
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="t"
/replace="tt"
/db_xref="dbSNP:1950701181"
variation 1971
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:935595520"
variation 1972..1975
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="gaga"
/replace="gagaga"
/db_xref="dbSNP:1950701113"
variation 1976..1978
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="cc"
/replace="ccc"
/db_xref="dbSNP:1418783722"
variation 1981
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950701021"
variation 1982
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1002477975"
variation 1989
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1278595598"
variation 1991
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1347878070"
variation 1992..1996
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="gggg"
/replace="ggggg"
/db_xref="dbSNP:1950700679"
variation 1992
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:541179525"
variation 1993
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1950700733"
variation 1996
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:576945941"
variation 1998
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:769326943"
variation 1999
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:892514179"
variation 2000
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1054288089"
variation 2005
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:367620504"
variation 2006
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:916367947"
variation 2009
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:973064787"
variation 2015
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1038910312"
variation 2016
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:963001005"
variation 2017..2018
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="cc"
/replace="ga"
/db_xref="dbSNP:796574941"
variation 2017
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950700117"
variation 2018
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:943323229"
variation 2020
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950699977"
variation 2021
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950699935"
variation 2025
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950699905"
variation 2028
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1950699872"
variation 2031
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:370314942"
variation 2032
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950699794"
variation 2033
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950699755"
variation 2034
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:182916402"
variation 2035
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:3741490"
variation 2040
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1443374356"
variation 2042
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950699663"
variation 2044
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2136906865"
variation 2046
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:983339952"
variation 2049
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:1950699592"
variation 2051
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1301770978"
variation 2057
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:987116079"
variation 2058
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950699497"
variation 2060
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:554895850"
variation 2062
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2136906816"
variation 2063
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950699427"
variation 2067
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1950699392"
variation 2072
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1298316988"
variation 2075
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950699320"
variation 2077
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:75237791"
variation 2078
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:746850522"
variation 2080
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1353265460"
variation 2081
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:777597930"
variation 2082
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:973165920"
variation 2086
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:758214417"
variation 2087
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:996057076"
variation 2089
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:192844482"
variation 2090..2094
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="gag"
/replace="gagag"
/db_xref="dbSNP:1423726431"
variation 2090
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:547619077"
variation 2096
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:2136906701"
variation 2098
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1010952147"
variation 2099
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1002451487"
variation 2102
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950698849"
variation 2105
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:893777773"
variation 2109
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1030977492"
variation 2111
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1163686844"
variation 2121
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950698740"
variation 2122
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1950698712"
variation 2123
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:781543889"
variation 2124
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:906815915"
variation 2125
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:2136906626"
variation 2128
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1415593537"
variation 2130
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1046993159"
variation 2140
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1334852400"
variation 2141
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:3741489"
variation 2147
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950698472"
variation 2150
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950698451"
variation 2151
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1270832087"
variation 2152
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1450666893"
variation 2154
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:4758909"
variation 2162
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1201112509"
variation 2165
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1192780707"
variation 2172
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1950698208"
variation 2176
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1258321216"
variation 2180
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:112870346"
variation 2182
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1593437106"
variation 2185
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1476204979"
variation 2186
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1163079471"
variation 2188
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1593437086"
variation 2191
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:754605513"
variation 2192
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:549889950"
variation 2195
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1458219528"
variation 2202
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1413405596"
variation 2203..2207
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="ag"
/replace="aggag"
/db_xref="dbSNP:1950697843"
variation 2210
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1037421988"
variation 2212..2214
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="gag"
/db_xref="dbSNP:1272645289"
variation 2212
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950697778"
variation 2216
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1053774837"
variation 2221
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1401470577"
variation 2225
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950697578"
variation 2226
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1231595234"
variation 2229
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1161815482"
variation 2234
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1950697422"
variation 2235
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1343788492"
variation 2236
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1593437040"
variation 2237
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:941773272"
variation 2238
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:907515157"
variation 2239
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:142376269"
variation 2242
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950697143"
variation 2244..2245
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="aa"
/replace="aaa"
/db_xref="dbSNP:36039891"
variation 2244
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950697092"
variation 2248
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950696998"
variation 2252
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1950696954"
variation 2255
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:933225060"
variation 2265
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1355291257"
variation 2267
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1223981564"
variation 2277
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:923251377"
variation 2278
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:1950696730"
variation 2279
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1950696680"
variation 2281
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:755120503"
variation 2282
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:2136906288"
variation 2284
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950696585"
variation 2285
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1566171220"
variation 2289
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:964542689"
variation 2293
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:1021425081"
variation 2299..2301
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="tt"
/replace="ttt"
/db_xref="dbSNP:1950696422"
variation 2299
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950696455"
variation 2306..2313
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="ctt"
/replace="cttatctt"
/db_xref="dbSNP:943198387"
variation 2306
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1950696399"
variation 2311
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:989498094"
variation 2316
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1215845332"
variation 2326
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950696268"
variation 2328
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1258077252"
variation 2329
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950696224"
variation 2330
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950696187"
variation 2332
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950696162"
variation 2334
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1296311836"
variation 2336
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2136906187"
variation 2340
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:958138392"
variation 2343
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950696070"
variation 2348..2354
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="aata"
/replace="aataata"
/db_xref="dbSNP:1950695982"
variation 2349..2358
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="ataat"
/replace="ataatataat"
/db_xref="dbSNP:1950695893"
variation 2351
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:1950696039"
variation 2353..2368
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="tataattta"
/replace="tataatttataattta"
/db_xref="dbSNP:1401013436"
variation 2353
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1486597998"
variation 2356
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950695953"
variation 2357
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:1593436977"
variation 2361
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950695859"
variation 2364
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1950695816"
variation 2365
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1030946220"
variation 2369
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950695735"
variation 2373
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1236969685"
variation 2376
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1950695685"
variation 2378
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:911779056"
variation 2379..2380
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="t"
/db_xref="dbSNP:1950695597"
variation 2379
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:1950695623"
variation 2380
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:1950695572"
variation 2381
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1179105860"
variation 2383
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1950695511"
variation 2385
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1406240647"
variation 2387
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:560709767"
variation 2388
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1950695431"
variation 2392
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:999568389"
variation 2394
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950695356"
variation 2396
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:548922117"
variation 2397
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1377843900"
variation 2398..2401
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="t"
/replace="tatt"
/db_xref="dbSNP:1950695202"
variation 2399
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:1950695263"
variation 2400
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950695232"
variation 2401..2404
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="ttga"
/db_xref="dbSNP:1950695140"
variation 2403
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1025188661"
variation 2404..2406
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="aa"
/replace="aaa"
/db_xref="dbSNP:1950695100"
variation 2412
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1331697816"
variation 2413
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:973134921"
variation 2414
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1012923039"
variation 2415
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:2136905955"
variation 2416
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950694997"
variation 2417
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:895287582"
variation 2419
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950694939"
variation 2420
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1950694917"
variation 2421
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2136905920"
variation 2422..2423
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="g"
/db_xref="dbSNP:34409499"
variation 2423
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1165063779"
variation 2428..2430
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="t"
/replace="tat"
/db_xref="dbSNP:1950694812"
variation 2429
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:2136905904"
variation 2430
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950694782"
variation 2432..2438
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="aaaaaaa"
/replace="aaaaaaaa"
/db_xref="dbSNP:1350044921"
variation 2432
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1374414628"
variation 2433
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:926776920"
variation 2438
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1280739400"
variation 2439
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1593436904"
variation 2442
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1593436894"
variation 2443
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:530330334"
variation 2444
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:971314022"
variation 2450
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1438398757"
variation 2451
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950694458"
variation 2465
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1950694435"
variation 2467
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1206923715"
variation 2468
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1231446323"
variation 2469
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1406251214"
variation 2471
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:941743070"
variation 2472
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950694296"
variation 2474
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:115799873"
variation 2475
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:541241838"
variation 2478
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950694155"
variation 2479
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:2136905761"
variation 2480
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950694126"
variation 2481
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950694099"
variation 2490
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1047424647"
variation 2492
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:932962176"
variation 2493
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:753996875"
variation 2494
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1211863620"
variation 2496
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950693980"
variation 2497
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1397721159"
variation 2498
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1489535422"
variation 2500
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1266210457"
variation 2503..2507
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="aaccg"
/db_xref="dbSNP:1950693729"
variation 2505..2506
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="atgctgctcccttgtgtgagtgaccacggccccgagcctggggctgga
cgcaggtcccagga"
/db_xref="dbSNP:1950693826"
variation 2505
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1316055975"
variation 2506..2507
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="acggccccgagcctggggctggacgcaggtcccaggacgtgct"
/db_xref="dbSNP:1441439409"
variation 2506
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:766575351"
variation 2507..2508
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="agcctggggctggacgcaggtcccaggacgtgctgctcccttct"
/replace="caggtcccaggacgtgctgctcccttct"
/replace="ctcccttct"
/replace="tgcattcccttct"
/replace="tgctgctcccttct"
/db_xref="dbSNP:rs1336309071"
variation 2508..2618
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="gtgagtgaccgcggccccgagcctggggctggacgcaggtcccaggac
"
/replace="gtgagtgaccgcggccccgagcctggggctggacgcaggtcccaggac
atgctgctcccttgtgtgagtgaccgcggccccgagcctggggctggacgcaggtccc
aggac"
/db_xref="dbSNP:1950691745"
variation 2508
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950693572"
variation 2508
/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 2509
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:974656529"
variation 2510
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1304579464"
variation 2513
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:1593436768"
variation 2515
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1593436758"
variation 2517
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:577007021"
variation 2518
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:60054929"
variation 2519..2555
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="cggccccgagcctggggctggacgcaggtcccaggac"
/replace="cggccccgagcctggggctggacgcaggtcccaggacgtgctgctccc
ttctgtgagtgaccacggccccgagcctggggctggacgcaggtcccaggac"
/db_xref="dbSNP:1566170955"
variation 2519
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:137860747"
variation 2520
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:543507917"
variation 2521
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1339972650"
variation 2523
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1950693259"
variation 2525
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:576425597"
variation 2526
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:978587251"
variation 2529..2530
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="cc"
/db_xref="dbSNP:1950693096"
variation 2529
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:970720837"
variation 2530
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950693066"
variation 2538
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1000902244"
variation 2541
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1025409954"
variation 2542
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1012477120"
variation 2543
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="cc"
/db_xref="dbSNP:1722609409"
variation 2548
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950692922"
variation 2549
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1452627569"
variation 2550
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1950692858"
variation 2552
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:899887350"
variation 2555
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950692769"
variation 2556
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:373137192"
variation 2557..2643
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="tgctgctcccttgtgtgagtgacc"
/replace="tgctgctcccttgtgtgagtgaccgcggccccgagcctggggctggac
gcaggtcccaggacgtgctgctcccttgtgtgagtgacc"
/db_xref="dbSNP:1950691334"
variation 2559
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:554677515"
variation 2562
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:377537751"
variation 2566
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1420814830"
variation 2568..2569
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="ac"
/db_xref="dbSNP:1950692612"
variation 2569
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:796139459"
variation 2570
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1006432643"
variation 2576
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1950692520"
variation 2579
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1396446600"
variation 2580..2581
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="acggccccgagcctggggctggacgcaggtcccaggacgtgctgctcc
cttctgtgagt"
/replace="acggccccgagcctggggctggacgcaggtcccaggacgtgctgctcc
cttctgtgagtgaccacggccccgagcctggggctggacgcaggtcccaggacatgct
gctcccttctgtgagt"
/replace="acggccccgagcctggggctggacgcaggtcccaggacgtgctgctcc
cttgtgtgagt"
/db_xref="dbSNP:1566170899"
variation 2580
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1384812230"
variation 2581..2582
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="acca"
/db_xref="dbSNP:1566170888"
variation 2581
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:15638"
variation 2582
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:111799372"
variation 2583
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:572274927"
variation 2585
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950692211"
variation 2586
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:997687935"
variation 2588
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:376925671"
variation 2589
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1039131607"
variation 2593
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950692083"
variation 2594..2644
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="tggggctggacgcaggtcccaggacgtgctgctcccttgtgtgagtga
cca"
/db_xref="dbSNP:1566170810"
variation 2594
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:373528706"
variation 2595
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1593436635"
variation 2599
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1354479573"
variation 2600
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="t"
/replace="tt"
/db_xref="dbSNP:1192334475"
variation 2604
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:369891917"
variation 2605
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1950691911"
variation 2606
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1950691881"
variation 2608
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1950691853"
variation 2609
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:867795922"
variation 2616
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:187667016"
variation 2618
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1186063298"
variation 2619
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:111786421"
variation 2620..2631
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="tgctgctccctt"
/replace="tgctgctcccttctgtgagtgaccacggccccgagcctggggctggac
gcaggtcccaggacatgctgctccctt"
/db_xref="dbSNP:1950691518"
variation 2620
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950691632"
variation 2622..2623
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="a"
/db_xref="dbSNP:1950691609"
variation 2624..2625
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="gc"
/db_xref="dbSNP:1950691577"
variation 2627
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1485012640"
variation 2631
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1054216011"
variation 2632
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:75167846"
variation 2635
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950691423"
variation 2636
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950691387"
variation 2639
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950691364"
variation 2644
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1456063340"
variation 2645
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:538873969"
variation 2646
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:117246365"
variation 2647..2659
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="gccccaagcccag"
/db_xref="dbSNP:1230976787"
variation 2647
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1566170789"
variation 2648
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950691154"
variation 2649
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950691128"
variation 2650
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1007364269"
variation 2651
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1218487646"
variation 2652
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:111338463"
variation 2653
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950690986"
variation 2657
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:978174785"
variation 2658
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:8021"
variation 2660
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:917908364"
variation 2665
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950690803"
variation 2667
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1332266605"
variation 2668
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:890301777"
variation 2669
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1301350623"
variation 2673
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1593436516"
variation 2675
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950690645"
variation 2678
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1950690593"
variation 2679
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1051667411"
variation 2680
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950690530"
variation 2681
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:991258229"
variation 2682
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:959608059"
variation 2683
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1016485269"
variation 2684
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1006486333"
variation 2686
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:73489148"
variation 2687
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950690229"
variation 2690
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1950690169"
variation 2691
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1364197764"
variation 2692
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1455110594"
variation 2700
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1026915435"
variation 2702
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1359866417"
variation 2703
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1566170710"
variation 2704
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1172254217"
variation 2705
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1468017193"
variation 2706
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1950689734"
variation 2707
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1376990440"
variation 2712
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950689662"
variation 2713
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:997254637"
variation 2716
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1395673079"
variation 2717
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1378783852"
variation 2722
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="cggtc"
/db_xref="dbSNP:1950689542"
variation 2725
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950689502"
variation 2726
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:941680964"
variation 2727
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="a"
/db_xref="dbSNP:2136904893"
variation 2729
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:535014873"
variation 2732
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1950689402"
variation 2737
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1950689380"
variation 2738
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950689346"
variation 2745..2757
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="tg"
/replace="tggcttccgcctg"
/db_xref="dbSNP:1950689207"
variation 2745
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:1238486499"
variation 2752
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1038687461"
variation 2753
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1007221366"
variation 2754
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:182104463"
variation 2757
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:980532486"
variation 2758
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1349314061"
variation 2760
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950689114"
variation 2762
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1213577280"
variation 2768
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1436173408"
variation 2770
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950689033"
variation 2771
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:764304023"
variation 2776
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2136904817"
variation 2779
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:566065778"
variation 2783
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1481966746"
variation 2786
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1950688911"
variation 2789
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2136904799"
variation 2790
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950688886"
variation 2794
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1950688853"
variation 2797
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1199546557"
variation 2800
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1950688798"
variation 2801
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:892808322"
variation 2802..2806
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="ttttt"
/replace="tttttt"
/db_xref="dbSNP:1950688694"
variation 2805
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:949556782"
variation 2807..2808
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="gg"
/db_xref="dbSNP:1176616028"
variation 2809..2816
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="aaaa"
/replace="aaaaaa"
/replace="aaaaaaa"
/replace="aaaaaaaa"
/replace="aaaaaaaaa"
/db_xref="dbSNP:rs957212862"
variation 2809
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1265543823"
variation 2810
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1054268966"
variation 2811
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:934594162"
variation 2812
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1488453973"
variation 2817
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:191072646"
variation 2818..2823
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="ttttt"
/replace="tttttt"
/replace="ttttttt"
/db_xref="dbSNP:1566170618"
variation 2820
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1256563011"
variation 2822..2828
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="tt"
/replace="ttatctt"
/db_xref="dbSNP:1950688278"
variation 2824
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:566122046"
variation 2827
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:949484292"
variation 2828
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1950688259"
variation 2829
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950688232"
variation 2841
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950688210"
variation 2842
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1018288530"
variation 2843
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1950688147"
variation 2844
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950688117"
variation 2849
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1299758456"
variation 2850
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:549120489"
variation 2858
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950688014"
variation 2863
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:918030300"
variation 2865
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:565128269"
variation 2869
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1458856890"
variation 2877..2884
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="cttct"
/replace="cttcttct"
/db_xref="dbSNP:1468716986"
variation 2878
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:937960418"
variation 2879
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:909224402"
variation 2880
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1226033314"
variation 2883
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1046106"
variation 2885
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950687714"
variation 2890
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1315555821"
variation 2891
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950687665"
variation 2892
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1279655347"
variation 2893
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1950687603"
variation 2894
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:985017981"
variation 2895
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1950687569"
variation 2902
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:1950687539"
variation 2903
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1432491382"
variation 2906
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:753726528"
variation 2908
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1950687442"
variation 2916
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1425798710"
variation 2918
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2136904528"
variation 2922
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950687386"
variation 2924
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:529547282"
variation 2927..2944
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="ctg"
/replace="ctgagaagcagcaatctg"
/db_xref="dbSNP:1950687169"
variation 2927
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:148270257"
variation 2929
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:11542904"
variation 2940
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:2136904496"
variation 2942
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:976689419"
variation 2943
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950687203"
variation 2944
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:2136904480"
variation 2945
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950687133"
variation 2946
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1950687101"
variation 2950
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:965819930"
variation 2952
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1950687045"
variation 2960
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="g"
/db_xref="dbSNP:897708347"
variation 2960
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1367604138"
variation 2963
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1037632913"
variation 2965
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950686909"
variation 2967
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950686881"
variation 2968
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950686849"
variation 2978
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:941651179"
variation 2979
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1046130"
regulatory 2981..2986
/regulatory_class="polyA_signal_sequence"
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
variation 2981
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1950686736"
variation 2982
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1950686709"
variation 2987
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:904877930"
variation 2988
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1017734390"
variation 2992
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:376262240"
variation 2993
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1007273719"
variation 2994
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:892777244"
variation 2995
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:561407931"
variation 2999
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1244757352"
variation 3001
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1298125618"
variation 3002
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:998710936"
variation 3004
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1950686377"
polyA_site 3005
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
ORIGIN
agctgagggagccgcaatgtctcttgacagcggcggcggcgcagccggttccgggttcggcgcggggcggggatgtgaatcccgatggagcggcccgaggaaggcaagcagtcgccgccgccgcagccctggggacggctcctgcgtctgggcgcggaggagggcgagccgcacgtcctcctgaggaagcgggagtggaccatcgggcggagacgaggttgcgacctttccttccccagcaataaactggtctctggagatcactgtagaattgtagtggatgaaaaatcaggtcaggtgacactggaagataccagcaccagtggaacagtgattaacaagctgaaggttgttaagaagcagacatgccctttacagactggggatgtcatctacttggtgtacaggaagaatgaaccggaacacaggtctgggggtggtggcatctcccctaaaggaagtggtccctctgtggcaagtgatgaagtctccagctttgcctcagctctcccagacagaaagactgcgtccttttcgtcgttggaaccccaggatcaggaggatttggagcccgtgaagaagaaaatgagaggagatggggaccttgacctgaacgggcagttgttggtcgcacaaccgcgtagaaatgcccaaaccgtccacgaggacgtcagagcagcggctgggaagccagacaagatggaggagacgctgacatgcatcatctgccaggacctgctgcacgactgcgtgagtttgcagccctgcatgcacacgttctgcgcggcttgctactcgggctggatggagcgctcgtccctgtgtcctacctgccgctgtcccgtggagcggatctgtaaaaaccacatcctcaacaacctcgtggaagcatacctcatccagcatccagacaagagtcgcagtgaagaagatgtgcaaagtatggatgccaggaataaaatcactcaagacatgctgcagcccaaagtcaggcggtctttttctgatgaagaagggagttcagaggacctgctggagctgtcagacgttgacagtgagtcctcagacattagccagccatacgtcgtgtgccggcagtgtcctgagtacagaaggcaggcggcgcagcctccccactgcccagcacccgagggcgagccaggagccccacaggccctgggggatgcaccctccacgtccgtcagcctgacgacagcagtccaggattacgtgtgccctctgcaaggaagccacgccctgtgcacctgctgcttccagcccatgcccgaccggagagcggagcgcgagcaggacccgcgtgtcgcccctcagcagtgtgcggtctgcctgcagcctttctgccacctgtactggggctgcacccggaccggctgctacggctgcctggccccgttttgtgagctcaacctgggtgacaagtgtctggacggcgtgctgaacaacaacagctacgagtcagacatcctgaagaattacctggcaaccagaggtttgacatggaaaaacatgttgaccgagagcctcgtggctctccagcggggagtgtttctgctgtctgattacagagtcacgggagacaccgttctgtgttactgctgtggcctgcgcagcttccgtgagctgacctatcagtatcggcagaacattcctgcttccgagttgccagtggccgtaacatcccgtcctgactgctactggggccgtaactgccgcactcaggtgaaagctcaccacgccatgaaattcaatcatatctgtgaacagacaaggttcaaaaactaagcatccagaggccctgagcagctttcagcactggaggtgaagagagcgtgtttttaaaatacagagacaagcacgtcaaggtgttttcacagccccctgagggaagggacgcagggtctccgacaggtgctctggggtgactcttctgtggagctttaccctctgagtgagaccctccccagagccccgggggccgcagcccgccctcctggtgagcgctgggcagggctcgtggtggcatcagcagcagagacgaagcctttctgtaacatgcggccgtcccgccgagaggggcagttttgctcttttgtacattttccgaaactacagttaaagcagaagtctgtttttaggaaaagtttcaagggagaagggcaagtttatcaaaaacattgtttcaggagaagggagcataagtttacagcctacaggacgtacacaatatcctgctgctgggaaaaccacagcattttatctattttttattttaataggtttggtgcttatcttctaataagatttaaatgtcacaaactgtagcacaaataatataatttataatttacaaattgactaaaattgggtatagtatggtatttgaaagaataagcatatgcttctgtttattaaaaaaagaaaccttccaatgtccaaaactgctaaccctcgacgtggccgccaagttagtcgctccttgctaaccggtgagtgaccgcggccccgagcctggggctggacgcaggtcccaggacatgctgctcccttgtgtgagtgaccgcggccccgagcctggggctggacgcaggtcccaggacgtgctgctcccttgtgtgagtgaccacggccccaagcccagggctggaggcaggtcccaggacgcgccgctccctcatgctgcccgggcccttcctccaagaccctacagagcctgaggggcaccttggcttccgcctgtgctagctttgccatgtcatctggaataatacttgaaattttgatttttggaaaaaaaagttttttatcttttgttgaaatcacctgttatccttgtttgtaaactgataacttttttgcttcttctcaggaatacagttttcaactgttgtcttgctcttgatagaaactgagaagcagcaatctgtatttgtggaggaaagtcctctcttttgcatattctaataaatgagccgcgtttgctcctcaaaaaaaaaa
//
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.
[Full Text]