ClinVar Miner

List of variants in gene combination RAD51D, RAD51L3-RFFL reported as likely benign for Breast-ovarian cancer, familial 4

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Total variants: 54
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HGVS dbSNP
NM_002878.3(RAD51D):c.-126C>T
NM_002878.3(RAD51D):c.-99T>C rs533209845
NM_002878.3(RAD51D):c.144+8C>T rs1060504766
NM_002878.3(RAD51D):c.145-13G>T rs760867838
NM_002878.3(RAD51D):c.145-14G>C rs200470533
NM_002878.3(RAD51D):c.145-4G>A rs201361465
NM_002878.3(RAD51D):c.145-9C>T rs1555570311
NM_002878.3(RAD51D):c.165G>C (p.Arg55=) rs1555570292
NM_002878.3(RAD51D):c.186G>A (p.Ser62=) rs746984258
NM_002878.3(RAD51D):c.198G>T (p.Val66=) rs200810304
NM_002878.3(RAD51D):c.216C>T (p.Tyr72=) rs148690585
NM_002878.3(RAD51D):c.231C>G (p.Thr77=) rs376670250
NM_002878.3(RAD51D):c.263+1455del rs979233150
NM_002878.3(RAD51D):c.263+1507_263+1509del rs753760360
NM_002878.3(RAD51D):c.263+1509C>T rs201506572
NM_002878.3(RAD51D):c.263+1551G>T
NM_002878.3(RAD51D):c.263+1570T>A rs376472075
NM_002878.3(RAD51D):c.263+1588A>G rs180869630
NM_002878.3(RAD51D):c.263+1596T>C rs1057517631
NM_002878.3(RAD51D):c.263+1597C>A rs755753106
NM_002878.3(RAD51D):c.263+1605G>A rs147933658
NM_002878.3(RAD51D):c.263+1612del rs750282687
NM_002878.3(RAD51D):c.263+1627C>T rs188981311
NM_002878.3(RAD51D):c.263+7G>A rs56218020
NM_002878.3(RAD51D):c.264-14del rs757481281
NM_002878.3(RAD51D):c.346-8A>T rs756059587
NM_002878.3(RAD51D):c.394G>A (p.Val132Ile) rs201141245
NM_002878.3(RAD51D):c.39C>G (p.Thr13=) rs146448657
NM_002878.3(RAD51D):c.481-10A>G rs1555568182
NM_002878.3(RAD51D):c.481-7G>A rs145832514
NM_002878.3(RAD51D):c.481-8C>T rs762247126
NM_002878.3(RAD51D):c.507G>A (p.Val169=) rs1555568162
NM_002878.3(RAD51D):c.549G>A (p.Gln183=) rs1555568122
NM_002878.3(RAD51D):c.567G>A (p.Val189=) rs373975416
NM_002878.3(RAD51D):c.577-10A>C rs1060504767
NM_002878.3(RAD51D):c.577-10A>G rs1060504767
NM_002878.3(RAD51D):c.606G>C (p.Val202=) rs1555567627
NM_002878.3(RAD51D):c.666A>G (p.Glu222=) rs114012742
NM_002878.3(RAD51D):c.668-4G>A rs1001440122
NM_002878.3(RAD51D):c.668-9C>T rs1555567544
NM_002878.3(RAD51D):c.694C>A (p.Arg232=) rs587780104
NM_002878.3(RAD51D):c.695G>A (p.Arg232Gln) rs28363283
NM_002878.3(RAD51D):c.698A>G (p.Glu233Gly) rs28363284
NM_002878.3(RAD51D):c.6C>A (p.Gly2=) rs1255954226
NM_002878.3(RAD51D):c.739-10T>C rs199998187
NM_002878.3(RAD51D):c.757C>A (p.Arg253=) rs137886232
NM_002878.3(RAD51D):c.75C>T (p.Ile25=) rs1555570482
NM_002878.3(RAD51D):c.771C>T (p.Ser257=) rs146212490
NM_002878.3(RAD51D):c.83-37C>A
NM_002878.3(RAD51D):c.888C>G (p.Ala296=) rs755177638
NM_002878.3(RAD51D):c.900A>G (p.Arg300=) rs370634278
NM_002878.3(RAD51D):c.904-11T>A rs374449943
NM_002878.3(RAD51D):c.957G>A (p.Gln319=) rs147669627
NM_002878.3(RAD51D):c.983C>T (p.Thr328Ile) rs138969595

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