ClinVar Miner

List of variants studied for Breast-ovarian cancer, familial 4 by Mendelics

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Total variants: 32
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HGVS dbSNP
NM_002878.3(RAD51D):c.-126C>T
NM_002878.3(RAD51D):c.1A>G (p.Met1Val) rs561425038
NM_002878.3(RAD51D):c.263+1509C>T rs201506572
NM_002878.3(RAD51D):c.263+1551G>T
NM_002878.3(RAD51D):c.263+1585C>G
NM_002878.3(RAD51D):c.263+1588A>G rs180869630
NM_002878.3(RAD51D):c.263+1605G>A rs147933658
NM_002878.3(RAD51D):c.263+1641C>T rs142387263
NM_002878.3(RAD51D):c.263+1644T>C
NM_002878.3(RAD51D):c.263+7G>A rs56218020
NM_002878.3(RAD51D):c.39C>G (p.Thr13=) rs146448657
NM_002878.3(RAD51D):c.475del (p.Glu159fs)
NM_002878.3(RAD51D):c.480+4A>G rs1567728211
NM_002878.3(RAD51D):c.481-8C>T rs762247126
NM_002878.3(RAD51D):c.556C>T (p.Arg186Ter) rs387906843
NM_002878.3(RAD51D):c.568G>A (p.Ala190Thr) rs80116829
NM_002878.3(RAD51D):c.667+2_667+23del
NM_002878.3(RAD51D):c.70A>G (p.Arg24Gly) rs781611267
NM_002878.3(RAD51D):c.793G>A (p.Gly265Arg) rs140285068
NM_002878.3(RAD51D):c.796C>T (p.Arg266Cys) rs587781813
NM_002878.3(RAD51D):c.83-37C>A
NM_002878.3(RAD51D):c.83-4T>A rs1567735916
NM_002878.3(RAD51D):c.839C>G (p.Thr280Ser) rs548111162
NM_002878.3(RAD51D):c.844G>A (p.Glu282Lys) rs1447892901
NM_002878.3(RAD51D):c.862G>C (p.Gly288Arg) rs1391505912
NM_002878.3(RAD51D):c.898C>T (p.Arg300Ter) rs750621215
NM_002878.3(RAD51D):c.900A>G (p.Arg300=) rs370634278
NM_002878.3(RAD51D):c.904-3C>T rs45478491
NM_002878.3(RAD51D):c.919G>A (p.Glu307Lys) rs115031549
NM_002878.3(RAD51D):c.957G>A (p.Gln319=) rs147669627
NM_002878.3(RAD51D):c.983C>T (p.Thr328Ile) rs138969595
NM_017559.4(FNDC8):c.121A>G (p.Met41Val)

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