ClinVar Miner

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

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Total variants: 19
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HGVS dbSNP
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.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.1513G>A (p.Ala505Thr) rs780179187
NM_000136.2(FANCC):c.1546_1547delGCinsTT (p.Ala516Phe) rs1554827162
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.767A>G (p.His256Arg) rs730881716
NM_000136.2(FANCC):c.800A>G (p.Asn267Ser) rs200854639
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.926T>G (p.Leu309Arg) rs1554832877
NM_000136.2(FANCC):c.934A>G (p.Ile312Val) rs1800366
NM_000136.2(FANCC):c.950T>G (p.Val317Gly) rs1438781491

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