ClinVar Miner

List of variants in gene combination LOC129390903, RAD51C reported as uncertain significance for breast-ovarian cancer, familial, susceptibility to, 3

Included ClinVar conditions (2):
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Total variants: 19
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HGVS dbSNP gnomAD frequency
NM_058216.3(RAD51C):c.640C>T (p.Arg214Cys) rs140804406 0.00017
NM_058216.3(RAD51C):c.635G>A (p.Arg212His) rs200857129 0.00004
NM_058216.3(RAD51C):c.601C>G (p.Leu201Val) rs531838785 0.00001
NM_058216.3(RAD51C):c.607A>G (p.Asn203Asp) rs538884532 0.00001
NM_058216.3(RAD51C):c.620A>G (p.His207Arg) rs587781921 0.00001
NM_058216.3(RAD51C):c.621T>A (p.His207Gln) rs786201848 0.00001
NM_058216.3(RAD51C):c.622A>G (p.Ile208Val) rs771078849 0.00001
NM_058216.3(RAD51C):c.634C>T (p.Arg212Cys) rs137947462 0.00001
NM_058216.3(RAD51C):c.641G>A (p.Arg214His) rs760911964 0.00001
NM_058216.3(RAD51C):c.656T>C (p.Leu219Ser) rs201529791 0.00001
NM_058216.3(RAD51C):c.602T>C (p.Leu201Pro) rs587780839
NM_058216.3(RAD51C):c.605A>G (p.Asp202Gly) rs1060502591
NM_058216.3(RAD51C):c.613C>A (p.Leu205Ile) rs2143797916
NM_058216.3(RAD51C):c.674T>C (p.Leu225Pro) rs1032681872
NM_058216.3(RAD51C):c.682G>A (p.Asp228Asn)
NM_058216.3(RAD51C):c.688C>T (p.Leu230Phe) rs751528808
NM_058216.3(RAD51C):c.696A>T (p.Glu232Asp) rs786201177
NM_058216.3(RAD51C):c.705+3A>G rs878855179
NM_058216.3(RAD51C):c.705G>T (p.Lys235Asn) rs755849719

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