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Previous release (v1)
2020-11-27 00:15:52, GGRNA.v2 : RefSeq release 202 (Sep, 2020)
LOCUS NM_001161346 11228 bp mRNA linear PRI 10-AUG-2020
DEFINITION Homo sapiens checkpoint with forkhead and ring finger domains
(CHFR), transcript variant 3, mRNA.
ACCESSION NM_001161346
VERSION NM_001161346.2
KEYWORDS RefSeq; MANE Select.
SOURCE Homo sapiens (human)
ORGANISM Homo sapiens
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi;
Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini;
Catarrhini; Hominidae; Homo.
REFERENCE 1 (bases 1 to 11228)
AUTHORS Cha Y, Kim SY, Yeo HY, Baek JY, Choi MK, Jung KH, Dong SM and Chang
HJ.
TITLE Association of CHFR Promoter Methylation with Treatment Outcomes of
Irinotecan-Based Chemotherapy in Metastatic Colorectal Cancer
JOURNAL Neoplasia 21 (1), 146-155 (2019)
PUBMED 30562637
REMARK GeneRIF: These data suggest that CHFR methylation may be associated
with favorable treatment outcomes of irinotecan-based chemotherapy
in patients with metastatic colorectal cancer.
REFERENCE 2 (bases 1 to 11228)
AUTHORS Woo SR, Lee HJ, Oh SJ, Kim S, Park SH, Lee J, Song KH and Kim TW.
TITLE Stabilization of HDAC1 via TCL1-pAKT-CHFR axis is a key element for
NANOG-mediated multi-resistance and stem-like phenotype in
immune-edited tumor cells
JOURNAL Biochem. Biophys. Res. Commun. 503 (3), 1812-1818 (2018)
PUBMED 30060952
REMARK GeneRIF: The results establish a firm molecular link in
immune-edited tumor cells among NANOG, AKT, CHFR, and HDAC1,
identifying HDAC1 as a molecular target in controlling NANOGHIGH
immune-refractory cancer.
REFERENCE 3 (bases 1 to 11228)
AUTHORS Zhou JD, Zhang TJ, Li XX, Ma JC, Guo H, Wen XM, Yao DM, Zhang W,
Lin J and Qian J.
TITLE Methylation-independent CHFR expression is a potential biomarker
affecting prognosis in acute myeloid leukemia
JOURNAL J. Cell. Physiol. 233 (6), 4707-4714 (2018)
PUBMED 29115660
REMARK GeneRIF: Lower CHFR expression was independently associated with
unfavorable prognosis in acute myeloid leukemia. Moreover, aberrant
CHFR promoter methylation was a rare event in myeloid malignances.
REFERENCE 4 (bases 1 to 11228)
AUTHORS Castellano L, Dabrowska A, Pellegrino L, Ottaviani S, Cathcart P,
Frampton AE, Krell J and Stebbing J.
TITLE Sustained expression of miR-26a promotes chromosomal instability
and tumorigenesis through regulation of CHFR
JOURNAL Nucleic Acids Res. 45 (8), 4401-4412 (2017)
PUBMED 28126920
REMARK GeneRIF: Re-expression of CHFR in miR-26a overexpressing cells
partially rescues normal mitosis and impairs the tumorigenesis
exerted by miR-26a.
REFERENCE 5 (bases 1 to 11228)
AUTHORS Kim M, Kwon YE, Song JO, Bae SJ and Seol JH.
TITLE CHFR negatively regulates SIRT1 activity upon oxidative stress
JOURNAL Sci Rep 6, 37578 (2016)
PUBMED 27883020
REMARK GeneRIF: JNK inhibitor prevents SIRT1 phosphorylation, leading to
elevated SIRT1 protein levels even in the presence of H2O2. Taken
together, our results indicate that CHFR plays a crucial role in
the cellular stress response pathway by controlling the stability
and function of SIRT1.
Publication Status: Online-Only
REFERENCE 6 (bases 1 to 11228)
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 11228)
AUTHORS Mizuno K, Osada H, Konishi H, Tatematsu Y, Yatabe Y, Mitsudomi T,
Fujii Y and Takahashi T.
TITLE Aberrant hypermethylation of the CHFR prophase checkpoint gene in
human lung cancers
JOURNAL Oncogene 21 (15), 2328-2333 (2002)
PUBMED 11948416
REFERENCE 8 (bases 1 to 11228)
AUTHORS Chaturvedi P, Sudakin V, Bobiak 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 11228)
AUTHORS Kang D, Chen J, Wong J and Fang G.
TITLE The checkpoint protein Chfr is a ligase that ubiquitinates Plk1 and
inhibits Cdc2 at the G2 to M transition
JOURNAL J. Cell Biol. 156 (2), 249-259 (2002)
PUBMED 11807090
REMARK GeneRIF: checkpoint protein Chfr is a ligase that ubiquitinates
Plk1 and inhibits Cdc2 at the G2 to M transition
REFERENCE 10 (bases 1 to 11228)
AUTHORS Scolnick 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 AC127070.10.
On Aug 2, 2019 this sequence version replaced NM_001161346.1.
Summary: This gene encodes an E3 ubiquitin-protein ligase required
for the maintenance of the antephase checkpoint that regulates cell
cycle entry into mitosis and, therefore, may play a key role in
cell cycle progression and tumorigenesis. The encoded protein has
an N-terminal forkhead-associated domain, a central RING-finger
domain, and a cysteine-rich C-terminal region. Alternatively
spliced transcript variants that encode different protein isoforms
have been described. [provided by RefSeq, Mar 2014].
Sequence Note: The RefSeq transcript and protein were derived from
genomic sequence to make the sequence consistent with the reference
genome assembly. The genomic coordinates used for the transcript
record were based on alignments.
Publication Note: This RefSeq record includes a subset of the
publications that are available for this gene. Please see the Gene
record to access additional publications.
##Evidence-Data-START##
Transcript exon combination :: SRR1803617.125085.1,
SRR1803615.188338.1 [ECO:0000332]
##Evidence-Data-END##
##RefSeq-Attributes-START##
RefSeq Select criteria :: based on conservation, expression
##RefSeq-Attributes-END##
COMPLETENESS: complete on the 3' end.
PRIMARY REFSEQ_SPAN PRIMARY_IDENTIFIER PRIMARY_SPAN COMP
1-59 AC127070.10 62213-62271
60-204 AC127070.10 62478-62622
205-304 AC127070.10 72164-72263
305-414 AC127070.10 77424-77533
415-474 AC127070.10 79035-79094
475-654 AC127070.10 80020-80199
655-822 AC127070.10 88184-88351
823-982 AC127070.10 90591-90750
983-1137 AC127070.10 92259-92413
1138-1300 AC127070.10 93188-93350
1301-1443 AC127070.10 96245-96387
1444-1563 AC127070.10 98081-98200
1564-1647 AC127070.10 101094-101177
1648-1718 AC127070.10 101663-101733
1719-1806 AC127070.10 102688-102775
1807-1914 AC127070.10 105684-105791
1915-1987 AC127070.10 106735-106807
1988-11228 AC127070.10 108222-117462
FEATURES Location/Qualifiers
source 1..11228
/organism="Homo sapiens"
/mol_type="mRNA"
/db_xref="taxon:9606"
/chromosome="12"
/map="12q24.33"
gene 1..11228
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/note="checkpoint with forkhead and ring finger domains"
/db_xref="GeneID:55743"
/db_xref="HGNC:HGNC:20455"
/db_xref="MIM:605209"
exon 1..59
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/inference="alignment:Splign:2.1.0"
variation 3
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:534357480"
variation 4
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:570446374"
variation 5
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:896280970"
variation 10
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1452969814"
variation 11
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1468914426"
variation 16
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1403273314"
variation 17..28
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="gcggcggcggcg"
/replace="gcggcggcggcggcg"
/db_xref="dbSNP:1462255454"
variation 17
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1052274666"
variation 19
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1023737356"
variation 22
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1177915172"
variation 23
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1305328622"
variation 24
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1043377910"
variation 25
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:942391667"
variation 26
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:910903529"
variation 27
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:986491943"
variation 28
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1593552393"
variation 30
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:867733545"
variation 31
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:866582582"
variation 32
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1184602056"
variation 33
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1457982394"
variation 34
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1180202481"
variation 36
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:955129324"
variation 37
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1418375663"
variation 39
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:918721775"
variation 40
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1379340094"
variation 41
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:558080896"
variation 42
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1401227842"
variation 45
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1203285887"
variation 46
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1373084089"
variation 47
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1460094658"
variation 49
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:972910573"
variation 50
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:962990830"
variation 55
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1210883392"
variation 56
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1261984726"
variation 58
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1318118652"
variation 59
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1307468722"
exon 60..204
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/inference="alignment:Splign:2.1.0"
misc_feature 63..65
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/note="upstream in-frame stop codon"
variation 68..70
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="cc"
/replace="ccc"
/db_xref="dbSNP:1000300479"
variation 68
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:756050840"
variation 69
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1200689283"
variation 70
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:745782659"
CDS 72..2030
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/EC_number="2.3.2.27"
/note="isoform 3 is encoded by transcript variant 3; RING
finger protein 196; checkpoint with forkhead and ring
finger domains, E3 ubiquitin protein ligase; RING-type E3
ubiquitin transferase CHFR"
/codon_start=1
/product="E3 ubiquitin-protein ligase CHFR isoform 3"
/protein_id="NP_001154818.1"
/db_xref="CCDS:CCDS53848.1"
/db_xref="GeneID:55743"
/db_xref="HGNC:HGNC:20455"
/db_xref="MIM:605209"
/translation="
MERPEEGKQSPPPQPWGRLLRLGAEEGEPHVLLRKREWTIGRRRGCDLSFPSNKLVSGDHCRIVVDEKSGQVTLEDTSTSGTVINKLKVVKKQTCPLQTGDVIYLVYRKNEPEHNVAYLYESLSEKQGMTQESFDTSGAGAGRGADPRVPPSSPATQVCFEEPQPSTSTSDLFPTASASSTEPSPAGRERSSSCGSGGGGISPKGSGPSVASDEVSSFASALPDRKTASFSSLEPQDQEDLEPVKKKMRGDGDLDLNGQLLVAQPRRNAQTVHEDVRAAAGKPDKMEETLTCIICQDLLHDCVSLQPCMHTFCAACYSGWMERSSLCPTCRCPVERICKNHILNNLVEAYLIQHPDKSRSEEDVQSMDARNKITQDMLQPKVRRSFSDEEGSSEDLLELSDVDSESSDISQPYVVCRQCPEYRRQAAQPPHCPAPEGEPGAPQALGDAPSTSVSLTTAVQDYVCPLQGSHALCTCCFQPMPDRRAEREQDPRVAPQQCAVCLQPFCHLYWGCTRTGCYGCLAPFCELNLGDKCLDGVLNNNSYESDILKNYLATRGLTWKNMLTESLVALQRGVFLLSDYRVTGDTVLCYCCGLRSFRELTYQYRQNIPASELPVAVTSRPDCYWGRNCRTQVKAHHAMKFNHICEQTRFKN"
misc_feature 117..386
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/note="Forkhead associated domain (FHA); found in
eukaryotic and prokaryotic proteins. Putative nuclear
signalling domain. FHA domains may bind phosphothreonine,
phosphoserine and sometimes phosphotyrosine. In
eukaryotes, many FHA domain-containing proteins...;
Region: FHA; cd00060"
/db_xref="CDD:238017"
misc_feature <162..>380
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/note="Forkhead associated (FHA) domain, binds pSer, pThr,
pTyr [Signal transduction mechanisms]; Region: FHA;
COG1716"
/db_xref="CDD:224630"
misc_feature order(195..197,234..236,240..245,306..314)
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/note="phosphopeptide binding site; other site"
/db_xref="CDD:238017"
misc_feature 765..767
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/note="Phosphoserine.
/evidence=ECO:0000244|PubMed:23186163; propagated from
UniProtKB/Swiss-Prot (Q96EP1.2); phosphorylation site"
misc_feature 942..1073
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/note="RING-finger (Really Interesting New Gene) domain, a
specialized type of Zn-finger of 40 to 60 residues that
binds two atoms of zinc; defined by the 'cross-brace'
motif C-X2-C-X(9-39)-C-X(1-3)-
H-X(2-3)-(N/C/H)-X2-C-X(4-48)C-X2-C; probably involved
in...; Region: RING; cd00162"
/db_xref="CDD:238093"
misc_feature order(945..947,954..956,993..995,999..1001,1008..1010,
1017..1019,1050..1052,1059..1061)
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/note="cross-brace motif; other site"
/db_xref="CDD:238093"
misc_feature 1191..1193
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/note="Phosphothreonine.
/evidence=ECO:0000250|UniProtKB:Q810L3; propagated from
UniProtKB/Swiss-Prot (Q96EP1.2); phosphorylation site"
variation 74
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1323042743"
variation 76
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:780919643"
variation 79
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:757065782"
variation 80
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:879451433"
variation 81
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1252988651"
variation 87
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1285867152"
variation 91
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1453369842"
variation 94
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1381686714"
variation 96
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1334460653"
variation 100..111
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="cgccgccgc"
/replace="cgccgccgccgc"
/replace="cgccgccgccgccgc"
/db_xref="dbSNP:765917829"
variation 100
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:752932212"
variation 102
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:372093401"
variation 104
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1566211828"
variation 105
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1459172597"
variation 108
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1022133046"
variation 109
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1407689006"
variation 110
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1415407421"
variation 113
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1184750358"
variation 114
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1444571399"
variation 116
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:547086677"
variation 118..121
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="ggg"
/replace="gggg"
/db_xref="dbSNP:1180924768"
variation 123
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1481059648"
variation 125
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1593551043"
variation 128
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1327949016"
variation 129
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1250940821"
variation 133
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1202757955"
variation 135
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1323574369"
variation 138
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1292594475"
variation 140
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1246548917"
variation 143
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:753867941"
variation 144
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1312590714"
variation 146
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1448675201"
variation 148
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1373843772"
variation 152
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1297235638"
variation 156
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:766461060"
variation 157
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1242357676"
variation 158
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:889736424"
variation 159
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1050716303"
variation 161
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1163686245"
variation 162
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1424534907"
variation 164
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:761126986"
variation 165
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:896897715"
variation 167
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1161017404"
variation 168
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:558346895"
variation 170
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1291046887"
variation 173
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:994965729"
variation 176
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1250327307"
variation 178
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1037164725"
variation 179
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1175632960"
variation 185
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1489596045"
variation 188
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1269637112"
variation 189
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1329871429"
variation 192
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1220935343"
variation 194
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1360131934"
variation 195
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:941122476"
variation 201
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1221878184"
exon 205..304
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/inference="alignment:Splign:2.1.0"
variation 206..207
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="t"
/replace="tt"
/db_xref="dbSNP:1566203316"
variation 208
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:762757910"
variation 209
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:775199616"
variation 210
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1016169013"
variation 213
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:370348872"
variation 216
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1184762410"
variation 219
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:776467669"
variation 221
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1371415158"
variation 222
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:765839818"
variation 223
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:770855105"
variation 225
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:146088609"
variation 228
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:77052806"
variation 231
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:540426488"
variation 236
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:771849929"
variation 241
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1325393287"
variation 244
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:573017098"
variation 245
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:780255609"
variation 246
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:956973617"
variation 249
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:756177652"
variation 250
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:1336502857"
variation 251
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1468386635"
variation 259
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:750466757"
variation 261
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:781107351"
variation 262
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:142824452"
variation 264
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1372280960"
variation 265
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:752104453"
variation 270
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1190933998"
variation 278
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1446377947"
variation 279
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:764607751"
variation 283
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:763356188"
variation 289
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1436266778"
variation 290
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:115711908"
variation 291
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1252203966"
variation 296
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1390531305"
variation 301
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1196075617"
variation 302
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:764905392"
variation 304
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:996565819"
exon 305..414
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/inference="alignment:Splign:2.1.0"
variation 307
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1405603798"
variation 308
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:200283117"
variation 317
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:138320999"
variation 320
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1262248032"
variation 328
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1403538188"
variation 329
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1593510822"
variation 336..341
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="gtt"
/replace="gttgtt"
/db_xref="dbSNP:749471534"
variation 338
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1026698840"
variation 345
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:753427887"
variation 347
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1409273260"
variation 348
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:765931951"
variation 349
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:145622325"
variation 350
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:896801495"
variation 357
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1220821081"
variation 364
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:773164146"
variation 366
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:1285340068"
variation 375
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1593510705"
variation 378
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1204882792"
variation 382
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:1349041006"
variation 384
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:767392115"
variation 386
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:761633567"
variation 387
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:774239471"
variation 392
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:768330210"
variation 400
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1281470229"
variation 402
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1036686943"
variation 404
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1277101257"
variation 406
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:377703818"
variation 407
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:771143796"
variation 411
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:201058448"
variation 412
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:778449705"
variation 414
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:758996497"
exon 415..474
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/inference="alignment:Splign:2.1.0"
variation 416
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:368692761"
variation 417
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:765096474"
variation 420
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1300704622"
variation 422
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:761045629"
variation 423
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1402185439"
variation 426
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:773555344"
variation 430
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:772208422"
variation 438
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1428337510"
variation 441
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1387598301"
variation 449
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1164831443"
variation 453
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:202105666"
variation 454
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:769092725"
variation 456
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1415955003"
variation 459
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1312795252"
variation 461
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:374502930"
variation 462
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:761297928"
variation 463
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1481092256"
variation 465
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:780460479"
variation 467
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:773617187"
variation 470
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1443614623"
exon 475..654
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/inference="alignment:Splign:2.1.0"
variation 475
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:1415698891"
variation 481..496
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="caggtgcagg"
/replace="caggtgcaggtgcagg"
/replace="caggtgcaggtgcaggtgcagg"
/db_xref="dbSNP:1566196191"
variation 485
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1345035376"
variation 489
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:529705996"
variation 490
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:968187911"
variation 491
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:1053846225"
variation 496
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1430015478"
variation 497
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1566196184"
variation 499
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:761341813"
variation 501..504
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="gggg"
/replace="ggggg"
/db_xref="dbSNP:1431549533"
variation 506
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1265155365"
variation 507
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:768775618"
variation 510
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:565366267"
variation 511
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1267263973"
variation 512
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:547367271"
variation 513
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:746187833"
variation 514
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:780923793"
variation 520
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1231852845"
variation 521
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1309985498"
variation 523
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1298364440"
variation 526
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1030329804"
variation 527
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:199790262"
variation 528
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1318983295"
variation 529
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:371470066"
variation 530
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:777219646"
variation 532
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1176037831"
variation 533
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1422710949"
variation 534
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:998173223"
variation 537
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1359228046"
variation 538
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:757969077"
variation 540
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:748110156"
variation 542
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:991093892"
variation 543
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:775208965"
variation 545
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1186481589"
variation 547
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1462519990"
variation 560
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1212965676"
variation 561
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1243354590"
variation 562
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:756710137"
variation 571
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:959491929"
variation 572
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:753235007"
variation 574
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:778929950"
variation 575
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:909400005"
variation 577
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1252563891"
variation 578
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:754853631"
variation 585
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1342113004"
variation 590
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1296093228"
variation 591
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:368788828"
variation 594
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1398898916"
variation 598
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:984493040"
variation 601
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1048846757"
variation 602
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:528825047"
variation 603
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:564810555"
variation 604
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1382340206"
variation 608
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:751789347"
variation 609
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1298843354"
variation 610
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:546136386"
variation 611
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1430290279"
variation 613
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:541715629"
variation 614
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:75391939"
variation 615
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1593503337"
variation 616
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1166700448"
variation 620
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1446218228"
variation 622..626
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="ct"
/replace="ctcct"
/db_xref="dbSNP:1593503293"
variation 624
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1385634222"
variation 629
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:965751134"
variation 632
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:563840755"
variation 633
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:745321936"
variation 634
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:776005190"
variation 639
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1042155534"
variation 640
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:765687815"
variation 645
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:1460603946"
variation 648
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1381533831"
variation 652
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1225450271"
exon 655..822
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/inference="alignment:Splign:2.1.0"
variation 658
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1038150337"
variation 660
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:370517411"
variation 663
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1438318944"
variation 664
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:777186106"
variation 666..667
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="gg"
/db_xref="dbSNP:1189456093"
variation 666
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:766667278"
variation 669
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:761034338"
variation 670
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1593482765"
variation 672
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:138637226"
variation 675
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1387477118"
variation 678
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:34220055"
variation 679
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:761525824"
variation 688
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:774070010"
variation 689
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:1419993206"
variation 691
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:201192149"
variation 692
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:989203291"
variation 698
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:796201985"
variation 699
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1163339779"
variation 707
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:749192848"
variation 711
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:374107669"
variation 713
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:769505625"
variation 718
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:780945230"
variation 735
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:35206714"
variation 738
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1366834805"
variation 740
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1038008124"
variation 742
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:560433355"
variation 747
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:201727566"
variation 752
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:758662673"
variation 753
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:533118486"
variation 754
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:150995074"
variation 755
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:755027328"
variation 758
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:908433616"
variation 761
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:200213031"
variation 763
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:754307363"
variation 764
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:145246258"
variation 766
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:141183005"
variation 767
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:767988129"
variation 768..769
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="t"
/replace="tt"
/db_xref="dbSNP:766718829"
variation 770
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1566189184"
variation 771
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1423637297"
variation 774..777
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="ccc"
/replace="cccc"
/db_xref="dbSNP:762524769"
variation 774
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:751592981"
variation 778
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:373754363"
variation 779
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:761615752"
variation 780
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:147803776"
variation 782
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:1566189143"
variation 788
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:774088595"
variation 789
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1472958431"
variation 797
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:768052255"
variation 799
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:762481129"
variation 800
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1025589682"
variation 801
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:775309126"
variation 803
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:764279540"
variation 805
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1463671908"
variation 807
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:974854406"
variation 810
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:1221100387"
variation 812
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:1238379063"
variation 814
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1566189061"
variation 819
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:745763828"
exon 823..982
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/inference="alignment:Splign:2.1.0"
variation 824
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:756088633"
variation 828
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:563202190"
variation 832
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1360404336"
variation 836
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:781748631"
variation 839
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:757715316"
variation 841
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:752016583"
variation 842
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:377318460"
variation 843
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:115096950"
variation 844
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1593477819"
variation 845
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1393923793"
variation 846..847
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="t"
/db_xref="dbSNP:776753889"
variation 847
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:1311480210"
variation 848
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:758139441"
variation 849
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:973250523"
variation 851
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1021390710"
variation 855
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:752281100"
variation 857
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:115431373"
variation 858
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:148618944"
variation 860
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:369526598"
variation 863
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:769878915"
variation 864
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:540759128"
variation 865
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:760584451"
variation 866
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:773102049"
variation 867
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:749537035"
variation 868
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:375174098"
variation 870
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:770024903"
variation 876
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:188170704"
variation 877
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:745889598"
variation 879
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:781395404"
variation 881
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:757876886"
variation 882
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1593477690"
variation 884
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:747517165"
variation 885
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:199761208"
variation 890
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1380131918"
variation 891
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:144838296"
variation 893
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1449844658"
variation 895
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1000960906"
variation 896
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:371434249"
variation 897
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:764757412"
variation 898
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="t"
/db_xref="dbSNP:768680290"
variation 898
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1464052810"
variation 900
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:754506935"
variation 901
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:149862277"
variation 905
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:765845584"
variation 907
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1277312621"
variation 908
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:746414469"
variation 909
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1341883561"
variation 911
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1295926976"
variation 913
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1306779303"
variation 915
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1593477559"
variation 916
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1375950961"
variation 920
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:35011845"
variation 921
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1341253353"
variation 926
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1312306793"
variation 927
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:767348322"
variation 929
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1352413194"
variation 937
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:761474515"
variation 938
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:775799321"
variation 944
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:1369689338"
variation 950
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:770185579"
variation 951
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1252007101"
variation 953
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:12315353"
variation 956
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:146107503"
variation 962
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1368629651"
variation 965
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1186411942"
variation 967
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:759798633"
variation 971
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1253421391"
variation 977
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:776915637"
variation 978
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:771123706"
variation 980
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1469130916"
exon 983..1137
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/inference="alignment:Splign:2.1.0"
variation 983
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:560066373"
variation 987
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1213141444"
variation 991
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:780721649"
variation 992
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:565644778"
variation 996
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:987211916"
variation 999
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1566185781"
variation 1000
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1174814592"
variation 1001
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1478670195"
variation 1003
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:751498855"
variation 1004
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:142975525"
variation 1007
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1466544467"
variation 1010
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:138280939"
variation 1011
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:754144763"
variation 1012
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:921635691"
variation 1013
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:766660009"
variation 1014
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:760933260"
variation 1015
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1221124973"
variation 1021
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:368405665"
variation 1022
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:767634272"
variation 1024
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:762287710"
variation 1025
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1367099211"
variation 1027
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:774770261"
variation 1032
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1433978124"
variation 1034
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:553735979"
variation 1035..1037
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="gag"
/replace="gagag"
/db_xref="dbSNP:1566185670"
variation 1036
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:968563777"
variation 1038
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:749601873"
variation 1039
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:775805064"
variation 1042
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1402056016"
variation 1043
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:769371058"
variation 1044
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1593473549"
variation 1046
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:745529097"
variation 1052
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:780623191"
variation 1056
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:535313174"
variation 1057
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:756736276"
variation 1059
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1474574138"
variation 1062
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:770034782"
variation 1063
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:146343801"
variation 1066
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1441931198"
variation 1068
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:571101753"
variation 1070
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:115029653"
variation 1071
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1344021759"
variation 1077
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:182092641"
variation 1078
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:756361707"
variation 1082
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1359376881"
variation 1084
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:141404869"
variation 1087
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:767497782"
variation 1089
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1313496770"
variation 1090
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1319716667"
variation 1091
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1339366523"
variation 1097
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:375199215"
variation 1102
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:774858017"
variation 1104
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1371529354"
variation 1105
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:764629991"
variation 1107
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1255988921"
variation 1109
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:191062458"
variation 1110
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:775898959"
variation 1113
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1182669640"
variation 1116
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1213131732"
variation 1117
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1241168194"
variation 1120
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1593473382"
variation 1121
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:148311652"
variation 1124
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:143181439"
variation 1125
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1241159400"
variation 1126
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1593473335"
variation 1127
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:770380694"
variation 1131
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:746470663"
variation 1132
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:370386571"
exon 1138..1300
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/inference="alignment:Splign:2.1.0"
variation 1139
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1227736511"
variation 1140..1141
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="aa"
/db_xref="dbSNP:777961507"
variation 1146
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1210874026"
variation 1148
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:928539042"
variation 1154
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1566184554"
variation 1161
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:879123151"
variation 1163
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1229649968"
variation 1165
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:777930523"
variation 1166
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1566184534"
variation 1168
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1293723698"
variation 1170
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:377225060"
variation 1174
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:748309050"
variation 1175
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:778828908"
variation 1176
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1434082116"
variation 1177
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:200764395"
variation 1178
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:369063253"
variation 1179
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:1026572995"
variation 1180
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:766865645"
variation 1181
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:2062163"
variation 1189
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1047280041"
variation 1190
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:750119581"
variation 1192
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:760238279"
variation 1194
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:761337268"
variation 1200
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:150467142"
variation 1208
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:763498728"
variation 1217
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:930183182"
variation 1218
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1322357484"
variation 1219
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:762961678"
variation 1220
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:879252133"
variation 1221
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:920205326"
variation 1222
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:201828860"
variation 1224
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1593470536"
variation 1225
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:769607729"
variation 1226
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:745615761"
variation 1229
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:776390811"
variation 1233
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:974463026"
variation 1236..1242
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="gaag"
/replace="gaagaag"
/db_xref="dbSNP:1434190222"
variation 1243
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:772321674"
variation 1246
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1315657949"
variation 1249
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1413044699"
variation 1253
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1353432969"
variation 1260
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1309789349"
variation 1265
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:748314312"
variation 1271
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1283784330"
variation 1274
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1395585538"
variation 1275
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1165776578"
variation 1285
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:779111370"
variation 1289
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1368718436"
variation 1298
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:754958760"
exon 1301..1443
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/inference="alignment:Splign:2.1.0"
variation 1304
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1286314037"
variation 1305
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1020597739"
variation 1307
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:748419509"
variation 1308
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:372270460"
variation 1309
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1013270057"
variation 1310
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1438322046"
variation 1311
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:768814594"
variation 1312
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1318363216"
variation 1313
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:749373830"
variation 1314
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:150627547"
variation 1316
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:368755833"
variation 1320
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1435723841"
variation 1321
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:746360566"
variation 1322
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1191956640"
variation 1328
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1451601823"
variation 1330
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:781699438"
variation 1333
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:757496767"
variation 1337
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1192492326"
variation 1341
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1445358565"
variation 1348
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:374229656"
variation 1349
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:777240371"
variation 1350
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1303770543"
variation 1351
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:371541325"
variation 1352
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:563852229"
variation 1356
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1231849613"
variation 1359
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1366854652"
variation 1360
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1270421677"
variation 1361
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1429332642"
variation 1363
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1176161885"
variation 1364
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:764723102"
variation 1374
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1237028076"
variation 1376
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:759529335"
variation 1377
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:753721064"
variation 1379
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1375184437"
variation 1381
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:367968934"
variation 1382
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:374006779"
variation 1383
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:774658371"
variation 1384
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1167629443"
variation 1385
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1566181842"
variation 1386
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:924051400"
variation 1387
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1593463729"
variation 1388
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1041545091"
variation 1392
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:768798394"
variation 1394
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1239336733"
variation 1409
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1189940191"
variation 1414
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:138207644"
variation 1415
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1593463695"
variation 1416
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1256747525"
variation 1418
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1379314322"
variation 1419
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:775767314"
variation 1422
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1196421815"
variation 1423
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:769933100"
variation 1424
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:746380972"
variation 1425
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:1215461680"
variation 1427
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:781511228"
variation 1428
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:141835819"
variation 1432
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:747380214"
variation 1435
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:778169456"
variation 1437
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:1355326421"
variation 1438
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:752333209"
variation 1439
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:536396076"
exon 1444..1563
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/inference="alignment:Splign:2.1.0"
variation 1444
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1402157616"
variation 1445
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:757077660"
variation 1448
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:146976267"
variation 1450
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:765605647"
variation 1451
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1408464611"
variation 1457
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:141349945"
variation 1458
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:776642806"
variation 1462
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1593459784"
variation 1463
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1306934237"
variation 1464
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:764423128"
variation 1467
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:766469365"
variation 1469
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:761102171"
variation 1474
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1304421220"
variation 1478
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:773703522"
variation 1479
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:772460210"
variation 1481
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:147791929"
variation 1482
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1454391193"
variation 1486
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1345653105"
variation 1487
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:116286061"
variation 1490
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:768361418"
variation 1491
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1593459724"
variation 1492
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1396714833"
variation 1493..1500
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="ctgct"
/replace="ctgctgct"
/db_xref="dbSNP:1363396811"
variation 1493
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:748952886"
variation 1494
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:763257394"
variation 1496
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1278317795"
variation 1503
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1593459675"
variation 1504
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:779441212"
variation 1505
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:775978433"
variation 1512
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1187706335"
variation 1514
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:781224248"
variation 1515
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:757239007"
variation 1516
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1593459653"
variation 1518
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:936864653"
variation 1519
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:969442993"
variation 1522
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:751440176"
variation 1525
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:2306541"
variation 1526
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:755310429"
variation 1527
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1298012137"
variation 1530
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:754035414"
variation 1531
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:944300584"
variation 1532
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:766376169"
variation 1533
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:150920425"
variation 1536
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1015010652"
variation 1537
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:773617183"
variation 1543
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:768065335"
variation 1544
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:142511371"
variation 1545
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:114117795"
variation 1546
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:201454195"
variation 1547
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1172173801"
variation 1548
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:200436687"
variation 1550
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:920038038"
variation 1551
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:746554223"
variation 1553
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:973207321"
variation 1557
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1486915053"
variation 1559
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1346472721"
variation 1560
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1258850426"
variation 1562
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:769207559"
exon 1564..1647
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/inference="alignment:Splign:2.1.0"
variation 1566
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:372012714"
variation 1567
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:201350082"
variation 1568
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:7975454"
variation 1571
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:375656978"
variation 1577
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1335016856"
variation 1579
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:201237898"
variation 1580
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1442703181"
variation 1581
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:765505226"
variation 1582
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1324580295"
variation 1591
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1403110794"
variation 1598
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:759242088"
variation 1603
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:953787024"
variation 1607
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:546055046"
variation 1608
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1593453012"
variation 1609
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:766020195"
variation 1611
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:371092913"
variation 1612
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:146156998"
variation 1613
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1454840670"
variation 1614
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:979112170"
variation 1615
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1252629926"
variation 1616
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:772089817"
variation 1617
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1448818469"
variation 1619
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1593452935"
variation 1622
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1249069969"
variation 1624
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:767140702"
variation 1625
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:765611625"
variation 1626
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1349644861"
variation 1631
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:189987561"
variation 1632
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1236250946"
variation 1634
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:966632867"
variation 1638
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1348083185"
variation 1639
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1302248351"
variation 1640
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1433674477"
variation 1643
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1327743680"
exon 1648..1718
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/inference="alignment:Splign:2.1.0"
variation 1649
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:777921940"
variation 1655
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:200853567"
variation 1658
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:748721756"
variation 1659
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1179840200"
variation 1664
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1471040037"
variation 1667
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1415191475"
variation 1669
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1233090445"
variation 1676
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:372404283"
variation 1677
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:755522022"
variation 1678
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:754297675"
variation 1679
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1323808548"
variation 1688
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1213796881"
variation 1689
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:780565079"
variation 1690
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1288355908"
variation 1693
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1225827826"
variation 1694
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:755891788"
variation 1696
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1288380542"
variation 1700
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:749973618"
variation 1702
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:1379904886"
variation 1703
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:767082498"
variation 1709
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1416698488"
variation 1713
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:761176081"
variation 1718
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1326600805"
exon 1719..1806
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/inference="alignment:Splign:2.1.0"
variation 1720
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1432073088"
variation 1724
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1422500887"
variation 1725
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:899072283"
variation 1726
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1008556440"
variation 1731
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:776466473"
variation 1735
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:576074865"
variation 1740
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:2306537"
variation 1745
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:536151635"
variation 1746
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1281285798"
variation 1747
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1378971375"
variation 1749..1753
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="aaaaa"
/replace="aaaaaa"
/db_xref="dbSNP:1224656808"
variation 1753
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1232869629"
variation 1755
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:200187965"
variation 1763
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:749821203"
variation 1764
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:780655269"
variation 1770
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:770399858"
variation 1772
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:899313894"
variation 1773
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:2306536"
variation 1776
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1485801990"
variation 1777
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:781614371"
variation 1778
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:756917083"
variation 1783
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1313082363"
variation 1784
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1465200907"
variation 1785
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1357095646"
variation 1786
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:558156375"
variation 1793
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1363290036"
variation 1797
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="c"
/db_xref="dbSNP:1428595949"
variation 1804
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1423530802"
exon 1807..1914
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/inference="alignment:Splign:2.1.0"
variation 1807
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1265969471"
variation 1819
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:115684143"
variation 1820
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1222086097"
variation 1829
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:115566777"
variation 1830
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:758025460"
variation 1832
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:976650599"
variation 1833
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:747697880"
variation 1834
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:1566173893"
variation 1840
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1356919481"
variation 1842
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:778392987"
variation 1843
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:754931883"
variation 1844
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1442480016"
variation 1853
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:937547511"
variation 1854
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:961309862"
variation 1855
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:557461509"
variation 1856
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1456695524"
variation 1858
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:766096241"
variation 1863
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:376798546"
variation 1869
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1439266364"
variation 1873
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:764448295"
variation 1875
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1220708351"
variation 1877
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1195509679"
variation 1879
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:114483951"
variation 1884
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:775769340"
variation 1885
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:144644143"
variation 1904
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:373411620"
variation 1905
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:777155485"
variation 1911
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:76224039"
exon 1915..1987
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/inference="alignment:Splign:2.1.0"
variation 1919
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:772354359"
variation 1920
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:761464761"
variation 1921
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="t"
/replace="tt"
/db_xref="dbSNP:1476434657"
variation 1923
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1425682767"
variation 1926
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1593440414"
variation 1928
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1194364986"
variation 1934
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:774002945"
variation 1937
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1260717996"
variation 1938
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1212784968"
variation 1943
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:768078789"
variation 1950
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:192495200"
variation 1951
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:779420556"
variation 1957..1961
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="gc"
/replace="gccgc"
/db_xref="dbSNP:1218603125"
variation 1959
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:769922499"
variation 1960
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:745735958"
variation 1963
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1339131647"
variation 1966
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:1188833829"
variation 1968
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1295444518"
variation 1970
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1449229353"
variation 1976
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1340024053"
variation 1982
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:146332668"
variation 1983
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:371841032"
variation 1985
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1401175113"
variation 1986
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:752894210"
variation 1987
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:779235326"
exon 1988..11228
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/inference="alignment:Splign:2.1.0"
variation 1994
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1456116703"
variation 1996
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:549826875"
variation 1999
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1223009144"
variation 2000
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:772496941"
variation 2013
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1288110354"
variation 2014
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1190631767"
variation 2018
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:200441646"
variation 2031
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1242787279"
variation 2038
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:776670620"
variation 2039
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:770961851"
variation 2041
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1566171705"
variation 2042
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1238046110"
variation 2045
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:746869999"
variation 2046
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:777416500"
variation 2047
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:755292850"
variation 2048
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:973123804"
variation 2050
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:375664747"
variation 2053..2055
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="tt"
/replace="ttt"
/db_xref="dbSNP:1566171684"
variation 2056
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:780118329"
variation 2060
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1293032557"
variation 2061
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:756135373"
variation 2067
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:750955936"
variation 2068
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:1157735470"
variation 2069
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:531300162"
variation 2072
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:757695645"
variation 2073
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:113800546"
variation 2076
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:752032125"
variation 2077
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:549782692"
variation 2078
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:762683133"
variation 2095
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1314603974"
variation 2099
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:1353651008"
variation 2100
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1286369531"
variation 2101
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1045979"
variation 2104
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:954494653"
variation 2105
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:749186808"
variation 2107
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1283042988"
variation 2110
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1237120100"
variation 2111
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1348995249"
variation 2113
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1593437486"
variation 2116
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1030178377"
variation 2128
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:925838751"
variation 2131
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1361292300"
variation 2133
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1593437462"
variation 2137
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:974644686"
variation 2140
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:567430632"
variation 2141
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1341331550"
variation 2145
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:911586191"
variation 2148
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:542153503"
variation 2151
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1156419163"
variation 2152
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1435059615"
variation 2153
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1593437426"
variation 2155
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:370209943"
variation 2157
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:950536054"
variation 2162
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:559705268"
variation 2164
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1010901456"
variation 2168
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1298882440"
variation 2170
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:893810615"
variation 2176
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:963549804"
variation 2185..2187
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="ttt"
/replace="ttttt"
/db_xref="dbSNP:3832804"
variation 2188
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:1593437365"
variation 2189
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:111820152"
variation 2190
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1052601435"
variation 2192
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1414983132"
variation 2198
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:935595520"
variation 2203..2205
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="cc"
/replace="ccc"
/db_xref="dbSNP:1418783722"
variation 2209
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1002477975"
variation 2216
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1278595598"
variation 2218
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1347878070"
variation 2219
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:541179525"
variation 2223
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:576945941"
variation 2225
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:769326943"
variation 2226
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:892514179"
variation 2227
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1054288089"
variation 2232
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:367620504"
variation 2233
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:916367947"
variation 2236
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:973064787"
variation 2242
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1038910312"
variation 2243
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:963001005"
variation 2244..2245
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="cc"
/replace="ga"
/db_xref="dbSNP:796574941"
variation 2245
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:943323229"
variation 2258
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:370314942"
variation 2261
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:182916402"
variation 2262
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:3741490"
variation 2267
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1443374356"
variation 2273
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:983339952"
variation 2278
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1301770978"
variation 2284
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:987116079"
variation 2287
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:554895850"
variation 2299
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1298316988"
variation 2304
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:75237791"
variation 2305
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:746850522"
variation 2307
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1353265460"
variation 2308
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:777597930"
variation 2309
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:973165920"
variation 2313
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:758214417"
variation 2314
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:996057076"
variation 2316
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:192844482"
variation 2317..2321
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="gag"
/replace="gagag"
/db_xref="dbSNP:1423726431"
variation 2317
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:547619077"
variation 2325
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1010952147"
variation 2326
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1002451487"
variation 2332
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:893777773"
variation 2336
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1030977492"
variation 2338
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1163686844"
variation 2350
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:781543889"
variation 2351
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:906815915"
variation 2355
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1415593537"
variation 2357
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1046993159"
variation 2367
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1334852400"
variation 2368
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:3741489"
variation 2378
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1270832087"
variation 2379
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1450666893"
variation 2381
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:4758909"
variation 2389
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1201112509"
variation 2392
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1192780707"
variation 2403
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1258321216"
variation 2407
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:112870346"
variation 2409
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1593437106"
variation 2412
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1476204979"
variation 2413
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1163079471"
variation 2415
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1593437086"
variation 2418
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:754605513"
variation 2419
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:549889950"
variation 2422
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1458219528"
variation 2429
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1413405596"
variation 2437
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1037421988"
variation 2439..2441
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="gag"
/db_xref="dbSNP:1272645289"
variation 2443
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1053774837"
variation 2448
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1401470577"
variation 2453
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1231595234"
variation 2456
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1161815482"
variation 2462
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1343788492"
variation 2463
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1593437040"
variation 2464
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:941773272"
variation 2465
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:907515157"
variation 2466
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:142376269"
variation 2471..2472
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="aa"
/replace="aaa"
/db_xref="dbSNP:36039891"
variation 2482
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:933225060"
variation 2492
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1355291257"
variation 2494
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1223981564"
variation 2504
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:923251377"
variation 2508
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:755120503"
variation 2512
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1566171220"
variation 2516
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:964542689"
variation 2520
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:1021425081"
variation 2533..2540
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="ctt"
/replace="cttatctt"
/db_xref="dbSNP:943198387"
variation 2538
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:989498094"
variation 2543
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1215845332"
variation 2555
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1258077252"
variation 2561
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1296311836"
variation 2567
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:958138392"
variation 2580..2595
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="tataattta"
/replace="tataatttataattta"
/db_xref="dbSNP:1401013436"
variation 2580
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1486597998"
variation 2584
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:1593436977"
variation 2592
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1030946220"
variation 2600
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1236969685"
variation 2605
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:911779056"
variation 2608
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1179105860"
variation 2612
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1406240647"
variation 2614
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:560709767"
variation 2619
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:999568389"
variation 2623
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:548922117"
variation 2624
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1377843900"
variation 2630
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1025188661"
variation 2639
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1331697816"
variation 2640
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:973134921"
variation 2641
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1012923039"
variation 2644
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:895287582"
variation 2649..2650
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="g"
/db_xref="dbSNP:34409499"
variation 2650
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1165063779"
variation 2659..2665
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="aaaaaaa"
/replace="aaaaaaaa"
/db_xref="dbSNP:1350044921"
variation 2659
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1374414628"
variation 2660
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:926776920"
variation 2665
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1280739400"
variation 2666
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1593436904"
variation 2669
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1593436894"
variation 2670
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:530330334"
variation 2671
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:971314022"
variation 2677
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1438398757"
variation 2694
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1206923715"
variation 2695
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1231446323"
variation 2696
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1406251214"
variation 2698
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:941743070"
variation 2701
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:115799873"
variation 2702
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:541241838"
variation 2717
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1047424647"
variation 2719
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:932962176"
variation 2720
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:753996875"
variation 2721
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1211863620"
variation 2724
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1397721159"
variation 2725
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1489535422"
variation 2727
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="g"
/db_xref="dbSNP:1215337863"
variation 2727
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1266210457"
variation 2732
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1316055975"
variation 2733..2734
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="acggccccgagcctggggctggacgcaggtcccaggacgtgct"
/db_xref="dbSNP:1441439409"
variation 2733
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:766575351"
variation 2734..2735
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="ctcccttct"
/db_xref="dbSNP:1336309071"
variation 2735
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="gacatgctgctcccttgtgtgagtgaccacggccccgagcctggggct
ggacgcaggtcccaggacgtgctgctcccttctg"
/db_xref="dbSNP:1566171025"
variation 2736
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:974656529"
variation 2737
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1304579464"
variation 2740
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:1593436768"
variation 2742
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1593436758"
variation 2744
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:577007021"
variation 2745
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:60054929"
variation 2746..2785
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="cggccccgagcctggggctggacgcaggtcccaggacatg"
/replace="cggccccgagcctggggctggacgcaggtcccaggacatgttgctccc
ttgtgtgagtgaccacggccccgagcctggggctggacgcaggtcccaggacgtgctg
ctcccttctgtgagtgaccacggccccgagcctggggctggacgcaggtcccaggaca
tg"
/db_xref="dbSNP:1566170943"
variation 2746..2782
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="cggccccgagcctggggctggacgcaggtcccaggac"
/replace="cggccccgagcctggggctggacgcaggtcccaggacgtgctgctccc
ttctgtgagtgaccacggccccgagcctggggctggacgcaggtcccaggac"
/db_xref="dbSNP:1566170955"
variation 2746
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:137860747"
variation 2747
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:543507917"
variation 2748
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1339972650"
variation 2752
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:576425597"
variation 2753
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:978587251"
variation 2756
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:970720837"
variation 2765
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1000902244"
variation 2768
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1025409954"
variation 2769
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1012477120"
variation 2776
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1452627569"
variation 2779
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:899887350"
variation 2783
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:373137192"
variation 2786
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:554677515"
variation 2789
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:377537751"
variation 2793
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1420814830"
variation 2796
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:796139459"
variation 2797
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1006432643"
variation 2806
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1396446600"
variation 2807..2808
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="acggccccgagcctggggctggacgcaggtcccaggacgtgctgctcc
cttctgtgagt"
/db_xref="dbSNP:1566170899"
variation 2807
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1384812230"
variation 2808..2809
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="acca"
/db_xref="dbSNP:1566170888"
variation 2808
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:15638"
variation 2809
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:111799372"
variation 2810
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:572274927"
variation 2813
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:997687935"
variation 2815
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:376925671"
variation 2816
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1039131607"
variation 2821..2871
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="tggggctggacgcaggtcccaggacgtgctgctcccttgtgtgagtga
cca"
/db_xref="dbSNP:1566170810"
variation 2821
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:373528706"
variation 2822
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1593436635"
variation 2826
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1354479573"
variation 2827
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="t"
/replace="tt"
/db_xref="dbSNP:1192334475"
variation 2831
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:369891917"
variation 2836
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:867795922"
variation 2843
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:187667016"
variation 2845
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1186063298"
variation 2846
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:111786421"
variation 2854
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1485012640"
variation 2858
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1054216011"
variation 2859
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:75167846"
variation 2871
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1456063340"
variation 2872
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:538873969"
variation 2873
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:117246365"
variation 2874..2886
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="gccccaagcccag"
/db_xref="dbSNP:1230976787"
variation 2874
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1566170789"
variation 2877
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1007364269"
variation 2878
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1218487646"
variation 2879
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:111338463"
variation 2884
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:978174785"
variation 2885
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:8021"
variation 2887
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:917908364"
variation 2894
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1332266605"
variation 2895
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:890301777"
variation 2896
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1301350623"
variation 2900
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1593436516"
variation 2906
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1051667411"
variation 2908
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:991258229"
variation 2909
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:959608059"
variation 2910
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1016485269"
variation 2911
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1006486333"
variation 2913
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:73489148"
variation 2918
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1364197764"
variation 2919
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1455110594"
variation 2927
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1026915435"
variation 2929
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/db_xref="dbSNP:1359866417"
variation 2930
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1566170710"
variation 2931
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1172254217"
variation 2932
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1468017193"
variation 2934
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1376990440"
variation 2940
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:997254637"
variation 2943
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1395673079"
variation 2944
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1378783852"
variation 2953
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:941680964"
variation 2956
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:535014873"
variation 2972
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="t"
/db_xref="dbSNP:1238486499"
variation 2979
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1038687461"
variation 2980
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1007221366"
variation 2981
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:182104463"
variation 2984
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:980532486"
variation 2985
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1349314061"
variation 2989
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1213577280"
variation 2995
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1436173408"
variation 2998
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:764304023"
variation 3006
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:566065778"
variation 3010
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1481966746"
variation 3024
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:1199546557"
variation 3028
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:892808322"
variation 3032
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:949556782"
variation 3034..3035
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="gg"
/db_xref="dbSNP:1176616028"
variation 3036..3043
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="aaaa"
/replace="aaaaaa"
/replace="aaaaaaa"
/replace="aaaaaaaa"
/replace="aaaaaaaaa"
/db_xref="dbSNP:rs957212862"
variation 3036
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1265543823"
variation 3037
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1054268966"
variation 3038
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:934594162"
variation 3039
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1488453973"
variation 3044
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:191072646"
variation 3045..3050
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="ttttt"
/replace="tttttt"
/db_xref="dbSNP:1566170618"
variation 3047
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1256563011"
variation 3051
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:566122046"
variation 3054
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:949484292"
variation 3069
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1018288530"
variation 3076
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1299758456"
variation 3077
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:549120489"
variation 3090
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:918030300"
variation 3092
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:565128269"
variation 3096
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1458856890"
variation 3104..3111
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="cttct"
/replace="cttcttct"
/db_xref="dbSNP:1468716986"
variation 3105
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:937960418"
variation 3106
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="g"
/replace="t"
/db_xref="dbSNP:909224402"
variation 3107
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1226033314"
variation 3110
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1046106"
variation 3117
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1315555821"
variation 3119
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1279655347"
variation 3121
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:985017981"
variation 3130
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1432491382"
variation 3133
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:753726528"
variation 3143
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1425798710"
variation 3151
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:529547282"
variation 3154
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:148270257"
variation 3156
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:11542904"
variation 3169
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:976689419"
variation 3177
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:965819930"
variation 3187
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace=""
/replace="g"
/db_xref="dbSNP:897708347"
variation 3187
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1367604138"
variation 3190
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1037632913"
variation 3205
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:941651179"
variation 3206
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1046130"
variation 3214
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:904877930"
variation 3215
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1017734390"
variation 3219
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:376262240"
variation 3220
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:1007273719"
variation 3221
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:892777244"
variation 3222
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="a"
/replace="g"
/db_xref="dbSNP:561407931"
variation 3226
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="g"
/db_xref="dbSNP:1244757352"
variation 3228
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:1298125618"
variation 3229
/gene="CHFR"
/gene_synonym="RNF116; RNF196"
/replace="c"
/replace="t"
/db_xref="dbSNP:998710936"
ORIGIN
gcaatgtctcttgacagcggcggcggcgcagccggttccgggttcggcgcggggcggggatgtgaatcccgatggagcggcccgaggaaggcaagcagtcgccgccgccgcagccctggggacggctcctgcgtctgggcgcggaggagggcgagccgcacgtcctcctgaggaagcgggagtggaccatcgggcggagacgaggttgcgacctttccttccccagcaataaactggtctctggagatcactgtagaattgtagtggatgaaaaatcaggtcaggtgacactggaagataccagcaccagtggaacagtgattaacaagctgaaggttgttaagaagcagacatgccctttacagactggggatgtcatctacttggtgtacaggaagaatgaaccggaacacaacgtggcatacctctatgaatctttaagtgaaaagcaaggcatgacacaagaatcctttgatacctcaggtgcaggtgcagggcgaggggccgatccccgggtccctccgtcgtcgcccgccactcaggtgtgctttgaggaaccacagccatcaacatcgacgtcagacctcttccccacagcctcggcctcttccacggagccttctcctgcagggcgagagcgttcctccagttgtgggtctgggggtggtggcatctcccctaaaggaagtggtccctctgtggcaagtgatgaagtctccagctttgcctcagctctcccagacagaaagactgcgtccttttcgtcgttggaaccccaggatcaggaggatttggagcccgtgaagaagaaaatgagaggagatggggaccttgacctgaacgggcagttgttggtcgcacaaccgcgtagaaatgcccaaaccgtccacgaggacgtcagagcagcggctgggaagccagacaagatggaggagacgctgacatgcatcatctgccaggacctgctgcacgactgcgtgagtttgcagccctgcatgcacacgttctgcgcggcttgctactcgggctggatggagcgctcgtccctgtgtcctacctgccgctgtcccgtggagcggatctgtaaaaaccacatcctcaacaacctcgtggaagcatacctcatccagcatccagacaagagtcgcagtgaagaagatgtgcaaagtatggatgccagaaataaaatcactcaagacatgctgcagcccaaagtcaggcggtctttttctgatgaagaagggagttcagaggacctgctggagctgtcagacgttgacagtgagtcctcagacattagccagccatacgtcgtgtgccggcagtgtcctgagtacagaaggcaggcggcgcagcctccccactgcccagcacccgagggcgagccaggagccccacaggccctgggggatgcaccctccacgtccgtcagcctgacgacagcagtccaggattacgtgtgccctctgcaaggaagccacgccctgtgcacctgctgcttccagcccatgcccgaccggagagcggagcgcgagcaggacccgcgtgtcgcccctcagcagtgtgcggtctgcctgcagcctttctgccacctgtactggggctgcacccggaccggctgctacggctgcctggccccgttttgtgagctcaacctgggtgacaagtgtctggacggcgtgctgaacaacaacagctacgagtcagacatcctgaagaattacctggcaaccagaggtttgacatggaaaaacatgttgaccgagagcctcgtggctctccagcggggagtgtttctgctgtctgattacagagtcacgggagacaccgttctgtgttactgctgtggcctgcgcagcttccgtgagctgacctatcagtatcggcagaacattcctgcttccgagttgccagtggccgtaacatcccgtcctgactgctactggggccgtaactgccgcactcaggtgaaagctcaccacgccatgaaattcaatcatatctgtgaacagacaaggttcaaaaactaagcatccagaggccctgagcagctttcagcactggaggtgaagagagcgtgtttttaaaatacagagacaagcacgtcaaggtgttttcacagccccctgagggaagggacgcagggtctccgacaggtgctctggggtgactcttctgtggagctttaccctctgagtgagaccctccccagagccccgggggccgcagcccgccctcctggtgagcgctgggcagggctcgtggtggcatcagcagcagagacgaagcctttctgtaacatgcggccgtcccgccgagaggggcagttttgctcttttgtacattttccgaaactacagttaaagcagaagtctgtttttaggaaaagtttcaagggagaagggcaagtttatcaaaaacattgtttcaggagaagggagcataagtttacagcctacaggacgtacacaatatcctgctgctgggaaaaccacagcattttatctattttttattttaataggtttggtgcttatcttctaataagatttaaatgtcacaaactgtagcacaaataatataatttataatttacaaattgactaaaattgggtatagtatggtatttgaaagaataagcatatgcttctgtttattaaaaaaagaaaccttccaatgtccaaaactgctaaccctcgacgtggccgccaagttagtcgctccttgctaaccggtgagtgaccgcggccccgagcctggggctggacgcaggtcccaggacatgctgctcccttgtgtgagtgaccgcggccccgagcctggggctggacgcaggtcccaggacgtgctgctcccttgtgtgagtgaccacggccccaagcccagggctggaggcaggtcccaggacgcgccgctccctcatgctgcccgggcccttcctccaagaccctacagagcctgaggggcaccttggcttccgcctgtgctagctttgccatgtcatctggaataatacttgaaattttgatttttggaaaaaaaagttttttatcttttgttgaaatcacctgttatccttgtttgtaaactgataacttttttgcttcttctcaggaatacagttttcaactgttgtcttgctcttgatagaaactgagaagcagcaatctgtatttgtggaggaaagtcctctcttttgcatattctaataaatgagccgcgtttgctcctccgctctcgtgttgggctcgtgtctggggctgcctcacttccccatgcgagggaggcaggccccatgcagagtgagctccgagtgcctcactgctagtgatggtcactctgtcacctgctgtccctcagtgactcctgtgaaacctgctcaggtctcttcattctgccaatgctgggaagccacaacctgttcatccagtgtggaggctttgtcttcagctgagcaccagaagaagccacaatgcagagaccctgagtttgtgcaagggtggggctgagaggggaggtcccgtgttagtgcaggggtgaggccgggaggggaggtcccgagtttgtgtaggggcgaggctgagcagggaggttctgagttagtgcaggggcgaggctgagcagggaggtcccgagttagtgcaggggcgaggctaagggggaggtcccaagtttgtgcaggggtgaggctgagcagggaggtcccaagttagtgcaggggcgaggctgagaggggagatcccgagtttgtgcaggggcgaggctgagaggggaggtccctagttagtgcaggggtgaggccgagaagggaggtcccaagtttgtgcatggatgaagccaaaaggggagtttgcacgtttgtgcaggggtgaggccaagaagggaagtcttgagttggtgcaggggtgagggagaggggaggtcctgagtttgtgcagaggcgaggctgagaggggaggtccctaagtgcaggggtgaggccgagaggggaggttgcaaatttgtgcaggggtgaggccaagaggggaggtcctgagttagtgcgggggtgaggccgagaggggaggtcctgagtttgtgcagaggcgaggctgagaggggaggtccttagtgcaggggtgaggctgagagggggaggtcccaagtttgtgcaggggtgaggccgaggggaggttgcaagtttgtgcaggggtgaggccaagaggggaggtcctgagttagtgcgggggtgaggccgagaggggagttcctgagtttgtgcagaggcgaggctgagaggggaggttgccagtttgtgcaggtgcgaggctgagaggggaggctggcattcgccaatgaagtgggctggggctaccctgcgtctgtgtcttagagagatcggttgatactcactcttccccttcccatctccaaaaagtagaaacaagaacacttgccctgtagaggatgctggtctttcctcaggaccagctgcacctgtccaggaagggcaggcagctcagagagcctctgggctccaggtgtcctagggactcactcctgcttccttagtccttcagagaagtccaactcctggcccactgtgaagaggatttctacctggagcagtcggaacagcttgggtttggctgtgatgtgagggaggaggccttgggagcagggcagttatcctcccagcgtggtaaggagccgtgttttatggaggcagggagatcagggcagttactcctcgggtgtggtaaggagctgtgttttatggaagcaggtggccgtgaactcattccgtcttttcatgagcttctgtacttcctcgtcctcaagacccagccatcccacccagcaaaactgaccggctgtggtggttttggagccctgctctccttgtggggtggctgcgtgggtcgtccacaggctttctggaggacagcctggtgctgctgcagatcccactgcttcttcctggctccttggcccagccttgggacaaacccagggcaggg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acctcccacagtgctgggattccaggcgtaagccgccacgcccagcaactccgtttcttacttgttggctcacattctcctgagaagtcctccctcaaccatcggcctgaaatagcagcgagcctccccagggttgcctctgccttttcttgactctttctgtcaccttctatgcttgttgtctggtccccactagaatataccttctgtaagagcagggatttgggacagtgcctagaatagtacttgcagacagtaggctacgataaatatgaatgacggccccatgcagatggtagcccctctcgctcgaacgcttcacccagttttattttcttttcatcagttaccgccctctgaaggtatccacacacaaacatgaaactggaccaaagcagggaccccccgcacgcagaatagtgctgggctcgcgtaaggcacctcagtgggtccatcagctgatgcatggacagacaaaatgggtgtatccagacactggagtatcgtgcagcgaggaaacgtgctgagtgtggatggaccttaaacacaccatgcaagtgaaaaggcgtcacagaaggccacatacgatatgatcccatttctatgaaatgtccagaagaggcacattcataaagacagaaggtgactgagtggttgtcgggctgggtggaggggatagggagtgaatgcaagaaggatccttctgaggtaacggaagtatccggaaactgggttggagtgatgggtgcacagctctgcacatttactacagtcgctgaactgcacacacaacacgggtatattttattgcatagaaattgtattaaagctgttaagaattttacttagattagcatttttcccacactgtgccatcaacttagtatatgattagattcattgtttctaactgtatttaaatttaatgtttgtcacattttgcttgctaaatttttaaaattttaaattactgtgggtacataaaaggtgtatatatttatggagtaccttgatattttaatacagacatacaatgtataatgatcaactcccagtaactggggtatccatcacctcaagcctgtatcatttctttgttaggaacattccagttccactctttttgttatttaaaaatatacaatacattattattaactatattcaccctcctgtgctatggaatactagatcttatgctaattaaatgttttccctatttctccca
//
by
@meso_cacase at
DBCLS
This page is licensed under a
Creative Commons Attribution 4.0 International License (CC BY 4.0).
If you use GGRNA in your work, please cite:
Naito Y, Bono H. (2012)
GGRNA: an ultrafast, transcript-oriented search engine for genes and transcripts.
Nucleic Acids Res., 40, W592-W596.
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