ClinVar Miner

List of variants in gene FANCE reported as uncertain significance for abdominal and pelvic region disorder

Included ClinVar conditions (902):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 79
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HGVS dbSNP
NM_021922.2(FANCE):c.*322C>T rs559999264
NM_021922.2(FANCE):c.*401G>C rs886061333
NM_021922.2(FANCE):c.*729A>G rs886061334
NM_021922.2(FANCE):c.-100C>T rs374493565
NM_021922.2(FANCE):c.-105C>T rs886061326
NM_021922.2(FANCE):c.-132A>G rs886061325
NM_021922.2(FANCE):c.-182G>A rs886061324
NM_021922.2(FANCE):c.-19G>C rs13215706
NM_021922.2(FANCE):c.1007T>C (p.Leu336Pro) rs886061330
NM_021922.2(FANCE):c.1018G>C (p.Gly340Arg) rs45524646
NM_021922.2(FANCE):c.1027C>T (p.Arg343Trp) rs567313440
NM_021922.2(FANCE):c.1057C>G (p.Pro353Ala) rs878855070
NM_021922.2(FANCE):c.1111C>T (p.Arg371Trp)
NM_021922.2(FANCE):c.1141C>T (p.Arg381Cys) rs371020401
NM_021922.2(FANCE):c.1189C>A (p.Pro397Thr) rs759782690
NM_021922.2(FANCE):c.1278G>A (p.Met426Ile)
NM_021922.2(FANCE):c.1290G>T (p.Glu430Asp) rs886061331
NM_021922.2(FANCE):c.1309A>G (p.Met437Val) rs746770705
NM_021922.2(FANCE):c.1316G>T (p.Gly439Val) rs776298967
NM_021922.2(FANCE):c.1331T>C (p.Leu444Pro) rs745685973
NM_021922.2(FANCE):c.1333C>T (p.Pro445Ser) rs141551053
NM_021922.2(FANCE):c.1336T>C (p.Trp446Arg) rs1554122137
NM_021922.2(FANCE):c.1378C>T (p.Arg460Trp) rs200535245
NM_021922.2(FANCE):c.1424A>G (p.Lys475Arg) rs200083899
NM_021922.2(FANCE):c.1459A>G (p.Met487Val) rs373735272
NM_021922.2(FANCE):c.1466A>T (p.Tyr489Phe)
NM_021922.2(FANCE):c.1509+3G>A
NM_021922.2(FANCE):c.1510-11C>T rs189384185
NM_021922.2(FANCE):c.1520C>T (p.Thr507Ile) rs1413425638
NM_021922.2(FANCE):c.1572G>A (p.Arg524=) rs115195341
NM_021922.2(FANCE):c.1582A>C (p.Lys528Gln) rs767896075
NM_021922.2(FANCE):c.1588G>A (p.Ala530Thr) rs377415237
NM_021922.2(FANCE):c.1591T>A (p.Leu531Met) rs147390386
NM_021922.2(FANCE):c.1593G>A (p.Leu531=) rs886061332
NM_021922.2(FANCE):c.1606C>G (p.Pro536Ala) rs1060501873
NM_021922.2(FANCE):c.1610G>T (p.Ter537Leu) rs139547269
NM_021922.2(FANCE):c.169C>T (p.Pro57Ser) rs1561787173
NM_021922.2(FANCE):c.175G>T (p.Asp59Tyr)
NM_021922.2(FANCE):c.206G>A (p.Arg69Gln) rs758238449
NM_021922.2(FANCE):c.214C>T (p.Pro72Ser) rs890865684
NM_021922.2(FANCE):c.216G>T (p.Pro72=) rs886061328
NM_021922.2(FANCE):c.229C>A (p.Pro77Thr) rs587778335
NM_021922.2(FANCE):c.253C>T (p.Pro85Ser) rs145068586
NM_021922.2(FANCE):c.274C>T (p.Arg92Trp) rs375195621
NM_021922.2(FANCE):c.298T>A (p.Ser100Thr) rs768911543
NM_021922.2(FANCE):c.311C>G (p.Ala104Gly) rs773580818
NM_021922.2(FANCE):c.316C>T (p.Arg106Trp) rs759034838
NM_021922.2(FANCE):c.31G>A (p.Ala11Thr) rs753304968
NM_021922.2(FANCE):c.356A>C (p.Gln119Pro)
NM_021922.2(FANCE):c.358A>G (p.Ile120Val)
NM_021922.2(FANCE):c.365A>T (p.Gln122Leu) rs1554121253
NM_021922.2(FANCE):c.397C>T (p.Leu133Phe) rs759124595
NM_021922.2(FANCE):c.400C>T (p.Arg134Cys) rs181761362
NM_021922.2(FANCE):c.436G>T (p.Val146Leu) rs755204532
NM_021922.2(FANCE):c.457G>A (p.Ala153Thr) rs151276683
NM_021922.2(FANCE):c.480C>A (p.Cys160Ter) rs45509302
NM_021922.2(FANCE):c.4G>C (p.Ala2Pro) rs886061327
NM_021922.2(FANCE):c.52C>T (p.Pro18Ser) rs552241929
NM_021922.2(FANCE):c.552A>C (p.Pro184=) rs138182352
NM_021922.2(FANCE):c.559G>A (p.Glu187Lys) rs142746353
NM_021922.2(FANCE):c.592G>A (p.Gly198Arg) rs747727711
NM_021922.2(FANCE):c.598C>T (p.Arg200Cys) rs763151358
NM_021922.2(FANCE):c.656G>T (p.Arg219Ile)
NM_021922.2(FANCE):c.65T>C (p.Leu22Pro)
NM_021922.2(FANCE):c.679G>A (p.Glu227Lys) rs1287242303
NM_021922.2(FANCE):c.696G>A (p.Glu232=) rs147356927
NM_021922.2(FANCE):c.746C>T (p.Ser249Phe)
NM_021922.2(FANCE):c.812C>T (p.Ala271Val) rs1060501874
NM_021922.2(FANCE):c.851T>C (p.Ile284Thr)
NM_021922.2(FANCE):c.856-3C>T rs749111562
NM_021922.2(FANCE):c.862C>T (p.Leu288Phe) rs886061329
NM_021922.2(FANCE):c.88_96CTGCAGGCG[1] (p.30_32LQA[1]) rs780106496
NM_021922.2(FANCE):c.929C>A (p.Pro310Gln) rs139600847
NM_021922.2(FANCE):c.929C>G (p.Pro310Arg) rs139600847
NM_021922.2(FANCE):c.953_958del (p.Glu318_Ser320delinsGly) rs1475613789
NM_021922.2(FANCE):c.968A>G (p.Gln323Arg)
NM_021922.2(FANCE):c.970-6A>T
NM_021922.2(FANCE):c.977T>G (p.Leu326Trp) rs779336261
NM_021922.2(FANCE):c.998T>C (p.Leu333Pro) rs770592868

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