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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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//

by @meso_cacase at DBCLS
This page is licensed under a Creative Commons Attribution 4.0 International License (CC BY 4.0).

If you use GGRNA in your work, please cite:
Naito Y, Bono H. (2012)
GGRNA: an ultrafast, transcript-oriented search engine for genes and transcripts.
Nucleic Acids Res., 40, W592-W596. [Full Text]