ClinVar Miner

List of variants in gene combination AOPEP, FANCC studied for Hereditary cancer-predisposing syndrome

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Total variants: 41
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HGVS dbSNP
NM_000136.2(FANCC):c.*5C>T rs117175949
NM_000136.2(FANCC):c.1073-4G>A rs147695697
NM_000136.2(FANCC):c.1073-5C>T rs375613884
NM_000136.2(FANCC):c.1090T>C (p.Trp364Arg) rs771694972
NM_000136.2(FANCC):c.1156T>C (p.Ser386Pro) rs41281202
NM_000136.2(FANCC):c.1179C>T (p.Ser393=) rs1328914149
NM_000136.2(FANCC):c.1244C>T (p.Ala415Val) rs550462055
NM_000136.2(FANCC):c.1249G>A (p.Glu417Lys) rs140687953
NM_000136.2(FANCC):c.1288_1290delTAC (p.Tyr430del) rs1210997135
NM_000136.2(FANCC):c.1330-3C>T rs4647542
NM_000136.2(FANCC):c.1345G>A (p.Val449Met) rs1800367
NM_000136.2(FANCC):c.1394A>G (p.Gln465Arg) rs1800368
NM_000136.2(FANCC):c.1407G>A (p.Thr469=) rs79722116
NM_000136.2(FANCC):c.1425A>G (p.Thr475=) rs199739450
NM_000136.2(FANCC):c.1467C>T (p.His489=) rs1554828385
NM_000136.2(FANCC):c.1485G>A (p.Leu495=) rs56082100
NM_000136.2(FANCC):c.1494T>C (p.Ala498=) rs76895298
NM_000136.2(FANCC):c.1509G>A (p.Thr503=) rs144278080
NM_000136.2(FANCC):c.1513G>A (p.Ala505Thr) rs780179187
NM_000136.2(FANCC):c.1530C>T (p.Thr510=) rs372199352
NM_000136.2(FANCC):c.1546_1547delGCinsTT (p.Ala516Phe) rs1554827162
NM_000136.2(FANCC):c.1560C>T (p.His520=) rs150020474
NM_000136.2(FANCC):c.1575T>G (p.Phe525Leu) rs587779901
NM_000136.2(FANCC):c.1589T>C (p.Leu530Ser) rs766809608
NM_000136.2(FANCC):c.1603C>T (p.Arg535Cys) rs185822330
NM_000136.2(FANCC):c.1622C>T (p.Pro541Leu) rs1554827120
NM_000136.2(FANCC):c.1642C>T (p.Arg548Ter) rs104886457
NM_000136.2(FANCC):c.705C>T (p.Pro235=) rs141828876
NM_000136.2(FANCC):c.767A>G (p.His256Arg) rs730881716
NM_000136.2(FANCC):c.800A>G (p.Asn267Ser) rs200854639
NM_000136.2(FANCC):c.816C>T (p.Ile272=) rs55719336
NM_000136.2(FANCC):c.817G>A (p.Glu273Lys) rs143181565
NM_000136.2(FANCC):c.823T>C (p.Phe275Leu) rs745621828
NM_000136.2(FANCC):c.840G>A (p.Ser280=) rs34671520
NM_000136.2(FANCC):c.843+4C>T rs4647506
NM_000136.2(FANCC):c.926T>G (p.Leu309Arg) rs1554832877
NM_000136.2(FANCC):c.934A>G (p.Ile312Val) rs1800366
NM_000136.2(FANCC):c.946C>T (p.Gln316Ter) rs776529713
NM_000136.2(FANCC):c.950T>G (p.Val317Gly) rs1438781491
NM_000136.2(FANCC):c.973G>A (p.Ala325Thr) rs201407189
NM_000136.2(FANCC):c.996+1G>T rs370510954

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