ClinVar Miner

List of variants reported as likely benign for breast-ovarian cancer, familial, susceptibility to, 4 by Counsyl

Included ClinVar conditions (1):
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ClinVar version:
Total variants: 27
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HGVS dbSNP
NM_002878.3(RAD51D):c.-99T>C rs533209845
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.198G>T (p.Val66=) rs200810304
NM_002878.3(RAD51D):c.216C>T (p.Tyr72=) rs148690585
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+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.481-7G>A rs145832514
NM_002878.3(RAD51D):c.481-8C>T rs762247126
NM_002878.3(RAD51D):c.666A>G (p.Glu222=) rs114012742
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.739-10T>C rs199998187
NM_002878.3(RAD51D):c.757C>A (p.Arg253=) rs137886232
NM_002878.3(RAD51D):c.771C>T (p.Ser257=) rs146212490
NM_002878.3(RAD51D):c.904-11T>A rs374449943

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