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: 15
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HGVS dbSNP
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.1330-3C>T rs4647542
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.1530C>T (p.Thr510=) rs372199352
NM_000136.2(FANCC):c.1560C>T (p.His520=) rs150020474
NM_000136.2(FANCC):c.705C>T (p.Pro235=) rs141828876
NM_000136.2(FANCC):c.816C>T (p.Ile272=) rs55719336
NM_000136.2(FANCC):c.840G>A (p.Ser280=) rs34671520

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