ClinVar Miner

List of variants reported as uncertain significance for Breast-ovarian cancer, familial, susceptibility to, 4 by Fulgent Genetics, Fulgent Genetics

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Total variants: 32
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HGVS dbSNP gnomAD frequency
NM_002878.4(RAD51D):c.434G>A (p.Arg145His) rs147264215 0.00023
NM_002878.4(RAD51D):c.137C>G (p.Ser46Cys) rs587780102 0.00010
NM_002878.4(RAD51D):c.973G>A (p.Gly325Ser) rs587780106 0.00008
NM_002878.4(RAD51D):c.263+1641C>T rs142387263 0.00006
NM_002878.4(RAD51D):c.629C>T (p.Ala210Val) rs376855484 0.00006
NM_002878.4(RAD51D):c.715C>T (p.Arg239Trp) rs770250516 0.00006
NM_002878.4(RAD51D):c.493C>T (p.Arg165Trp) rs544654228 0.00004
NM_002878.4(RAD51D):c.793G>A (p.Gly265Arg) rs140285068 0.00004
NM_002878.4(RAD51D):c.796C>T (p.Arg266Cys) rs587781813 0.00004
NM_002878.4(RAD51D):c.878C>T (p.Ala293Val) rs769732230 0.00003
NM_002878.4(RAD51D):c.164G>A (p.Arg55Gln) rs151198586 0.00002
NM_002878.4(RAD51D):c.620C>T (p.Ser207Leu) rs370228071 0.00002
NM_002878.4(RAD51D):c.868C>T (p.Arg290Trp) rs527964137 0.00002
NM_002878.4(RAD51D):c.292T>A (p.Tyr98Asn) rs730881946 0.00001
NM_002878.4(RAD51D):c.557G>A (p.Arg186Gln) rs780491769 0.00001
NM_002878.4(RAD51D):c.607G>A (p.Val203Met) rs730881947 0.00001
NM_002878.4(RAD51D):c.716G>A (p.Arg239Gln) rs780921112 0.00001
NM_002878.4(RAD51D):c.80C>A (p.Thr27Lys) rs139642328 0.00001
NM_001142571.2(RAD51D):c.-279_-275del rs761104531
NM_002878.4(RAD51D):c.196G>T (p.Val66Leu) rs56026142
NM_002878.4(RAD51D):c.263+1521G>A
NM_002878.4(RAD51D):c.263+1551G>T rs780006577
NM_002878.4(RAD51D):c.263+1566G>A
NM_002878.4(RAD51D):c.265C>T (p.Leu89Phe) rs2142437449
NM_002878.4(RAD51D):c.270T>A (p.Asp90Glu) rs1567728766
NM_002878.4(RAD51D):c.349T>A (p.Cys117Ser) rs786201358
NM_002878.4(RAD51D):c.412A>G (p.Asn138Asp) rs141690729
NM_002878.4(RAD51D):c.559G>A (p.Gly187Ser) rs1474938268
NM_002878.4(RAD51D):c.680T>C (p.Met227Thr) rs773485482
NM_002878.4(RAD51D):c.802T>A (p.Trp268Arg) rs755965977
NM_002878.4(RAD51D):c.82+11G>A rs2091796813
NM_002878.4(RAD51D):c.874A>G (p.Met292Val) rs1555567076

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