ClinVar Miner

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

Included ClinVar conditions (1):
Minimum submission review status: Collection method:
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ClinVar version:
Total variants: 13
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HGVS dbSNP
NM_002878.3(RAD51D):c.1A>G (p.Met1Val) rs561425038
NM_002878.3(RAD51D):c.1A>T (p.Met1Leu) rs561425038
NM_002878.3(RAD51D):c.270_271dup (p.Lys91fs) rs753862052
NM_002878.3(RAD51D):c.363del (p.Ala122fs) rs730881935
NM_002878.3(RAD51D):c.451C>T (p.Gln151Ter) rs587781756
NM_002878.3(RAD51D):c.620C>T (p.Ser207Leu) rs370228071
NM_002878.3(RAD51D):c.649G>T (p.Gly217Ter) rs775365939
NM_002878.3(RAD51D):c.655C>T (p.Gln219Ter) rs771007945
NM_002878.3(RAD51D):c.6_13dup (p.Arg5fs) rs1555570506
NM_002878.3(RAD51D):c.740_741dup (p.Thr248Ter) rs1555567197
NM_002878.3(RAD51D):c.81del (p.Val28fs) rs1064793952
NM_002878.3(RAD51D):c.85del (p.Val29fs) rs1057517586
NM_002878.3(RAD51D):c.94_95del (p.Val32fs) rs786203137

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