ClinVar Miner

List of variants reported as uncertain significance for Fanconi anemia complementation group C by Mendelics

Included ClinVar conditions (2):
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Total variants: 18
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HGVS dbSNP
NM_000136.2(FANCC):c.1069C>G (p.Gln357Glu)
NM_000136.2(FANCC):c.1275C>G (p.Leu425=) rs767126985
NM_000136.2(FANCC):c.127G>A (p.Glu43Lys) rs374836770
NM_000136.2(FANCC):c.1363G>T (p.Ala455Ser) rs730881724
NM_000136.2(FANCC):c.1374A>C (p.Arg458Ser) rs56394801
NM_000136.2(FANCC):c.1495C>T (p.Pro499Ser)
NM_000136.2(FANCC):c.178G>A (p.Val60Ile) rs138629441
NM_000136.2(FANCC):c.202G>A (p.Gly68Ser)
NM_000136.2(FANCC):c.28T>G (p.Cys10Gly) rs147479204
NM_000136.2(FANCC):c.29G>A (p.Cys10Tyr) rs143152201
NM_000136.2(FANCC):c.395C>G (p.Ala132Gly) rs587779905
NM_000136.2(FANCC):c.413T>G (p.Leu138Arg)
NM_000136.2(FANCC):c.668T>C (p.Val223Ala) rs751410815
NM_000136.2(FANCC):c.817G>A (p.Glu273Lys) rs143181565
NM_000136.2(FANCC):c.839C>T (p.Ser280Leu) rs749230615
NM_000136.2(FANCC):c.843+5G>A rs369082921
NM_000136.2(FANCC):c.871T>C (p.Phe291Leu)
NM_000136.2(FANCC):c.934A>G (p.Ile312Val) rs1800366

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