ClinVar Miner

List of variants in gene combination AOPEP, FANCC reported as likely benign for Hereditary cancer-predisposing syndrome

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Total variants: 58
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HGVS dbSNP
NM_000136.3(FANCC):c.1000C>T (p.Arg334Trp) rs140348260
NM_000136.3(FANCC):c.1008A>G (p.Ala336=) rs1588070906
NM_000136.3(FANCC):c.1011C>G (p.Leu337=) rs1272166766
NM_000136.3(FANCC):c.1023T>C (p.Phe341=) rs758439579
NM_000136.3(FANCC):c.1035T>G (p.Ser345=) rs1057522277
NM_000136.3(FANCC):c.1059G>T (p.Leu353=) rs1588070620
NM_000136.3(FANCC):c.1063G>C (p.Asp355His) rs587778325
NM_000136.3(FANCC):c.1152T>C (p.His384=) rs748127093
NM_000136.3(FANCC):c.1156T>C (p.Ser386Pro) rs41281202
NM_000136.3(FANCC):c.1161C>T (p.Cys387=) rs548998258
NM_000136.3(FANCC):c.1170C>G (p.Pro390=) rs878853668
NM_000136.3(FANCC):c.1170C>T (p.Pro390=) rs878853668
NM_000136.3(FANCC):c.1179C>T (p.Ser393=) rs1328914149
NM_000136.3(FANCC):c.1242G>A (p.Ser414=) rs587780939
NM_000136.3(FANCC):c.1257C>A (p.Pro419=) rs878853669
NM_000136.3(FANCC):c.1260G>C (p.Thr420=) rs749709412
NM_000136.3(FANCC):c.1264C>T (p.Leu422=) rs756716463
NM_000136.3(FANCC):c.1269G>T (p.Leu423=) rs1588047986
NM_000136.3(FANCC):c.1290C>T (p.Tyr430=) rs766105286
NM_000136.3(FANCC):c.1330-3C>T rs4647542
NM_000136.3(FANCC):c.1344C>T (p.Ala448=) rs760983825
NM_000136.3(FANCC):c.1348C>T (p.Leu450=) rs1193661760
NM_000136.3(FANCC):c.1351G>A (p.Gly451Ser) rs141805918
NM_000136.3(FANCC):c.1353C>T (p.Gly451=) rs745338413
NM_000136.3(FANCC):c.1374A>C (p.Arg458Ser) rs56394801
NM_000136.3(FANCC):c.1394A>G (p.Gln465Arg) rs1800368
NM_000136.3(FANCC):c.1407G>A (p.Thr469=) rs79722116
NM_000136.3(FANCC):c.1425A>G (p.Thr475=) rs199739450
NM_000136.3(FANCC):c.1458G>T (p.Leu486=) rs1588029111
NM_000136.3(FANCC):c.1467C>T (p.His489=) rs1554828385
NM_000136.3(FANCC):c.1485G>A (p.Leu495=) rs56082100
NM_000136.3(FANCC):c.1488C>G (p.Leu496=) rs1057520505
NM_000136.3(FANCC):c.1494T>C (p.Ala498=) rs76895298
NM_000136.3(FANCC):c.1509G>A (p.Thr503=) rs144278080
NM_000136.3(FANCC):c.1530C>T (p.Thr510=) rs372199352
NM_000136.3(FANCC):c.1531C>T (p.Leu511=) rs1588028784
NM_000136.3(FANCC):c.1545T>C (p.Thr515=) rs1588008483
NM_000136.3(FANCC):c.1560C>T (p.His520=) rs150020474
NM_000136.3(FANCC):c.1604G>A (p.Arg535His) rs587779902
NM_000136.3(FANCC):c.1623T>G (p.Pro541=) rs375362894
NM_000136.3(FANCC):c.1629A>G (p.Ser543=) rs1352980665
NM_000136.3(FANCC):c.1660C>T (p.Leu554=) rs769743634
NM_000136.3(FANCC):c.1663C>A (p.Arg555=) rs370974124
NM_000136.3(FANCC):c.705C>T (p.Pro235=) rs141828876
NM_000136.3(FANCC):c.735G>T (p.Arg245=) rs1174763492
NM_000136.3(FANCC):c.816C>T (p.Ile272=) rs55719336
NM_000136.3(FANCC):c.839C>T (p.Ser280Leu) rs749230615
NM_000136.3(FANCC):c.840G>A (p.Ser280=) rs34671520
NM_000136.3(FANCC):c.867C>T (p.Ala289=) rs1588106727
NM_000136.3(FANCC):c.882T>C (p.Val294=) rs750639831
NM_000136.3(FANCC):c.888G>A (p.Glu296=) rs779166059
NM_000136.3(FANCC):c.906C>G (p.Leu302=) rs766079351
NM_000136.3(FANCC):c.909G>C (p.Leu303=) rs1588100992
NM_000136.3(FANCC):c.915C>T (p.Thr305=) rs138132690
NM_000136.3(FANCC):c.957G>A (p.Thr319=) rs1060504647
NM_000136.3(FANCC):c.972A>G (p.Glu324=) rs1261385032
NM_000136.3(FANCC):c.975T>G (p.Ala325=) rs747463354
NM_000136.3(FANCC):c.993G>A (p.Lys331=) rs748582850

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