ClinVar Miner

List of variants in gene combination AOPEP, FANCC reported as benign for not specified

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Gene type:
ClinVar version:
Total variants: 22
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HGVS dbSNP
NM_000136.3(FANCC):c.*42G>A rs7029888
NM_000136.3(FANCC):c.*5C>T rs117175949
NM_000136.3(FANCC):c.*7C>T rs372511678
NM_000136.3(FANCC):c.1073-5C>T rs375613884
NM_000136.3(FANCC):c.1155-38T>C rs4647534
NM_000136.3(FANCC):c.1156T>C (p.Ser386Pro) rs41281202
NM_000136.3(FANCC):c.1242G>A (p.Ser414=) rs587780939
NM_000136.3(FANCC):c.1290C>T (p.Tyr430=) rs766105286
NM_000136.3(FANCC):c.1329+111C>T rs527823099
NM_000136.3(FANCC):c.1329+175C>T rs112446681
NM_000136.3(FANCC):c.1329+212C>T rs41281200
NM_000136.3(FANCC):c.1330-3C>T rs4647542
NM_000136.3(FANCC):c.1345G>A (p.Val449Met) rs1800367
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.1485G>A (p.Leu495=) rs56082100
NM_000136.3(FANCC):c.1509G>A (p.Thr503=) rs144278080
NM_000136.3(FANCC):c.687-15A>C rs765327075
NM_000136.3(FANCC):c.705C>T (p.Pro235=) rs141828876
NM_000136.3(FANCC):c.816C>T (p.Ile272=) rs55719336
NM_000136.3(FANCC):c.840G>A (p.Ser280=) rs34671520
NM_000136.3(FANCC):c.897-19C>T rs368830981

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