ClinVar Miner

List of variants in gene combination RAD51D, RAD51L3-RFFL studied for Hereditary breast and ovarian cancer syndrome

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Total variants: 42
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HGVS dbSNP
NM_002878.3(RAD51D):c.109G>C (p.Glu37Gln) rs876659848
NM_002878.3(RAD51D):c.137C>G (p.Ser46Cys) rs587780102
NM_002878.3(RAD51D):c.146C>T (p.Ala49Val) rs140317560
NM_002878.3(RAD51D):c.164G>A (p.Arg55Gln) rs151198586
NM_002878.3(RAD51D):c.192C>T (p.Phe64=) rs1567735397
NM_002878.3(RAD51D):c.1A>G (p.Met1Val) rs561425038
NM_002878.3(RAD51D):c.232T>G (p.Ser78Ala) rs1567735315
NM_002878.3(RAD51D):c.263+1450T>A rs1567734484
NM_002878.3(RAD51D):c.263+1509C>T rs201506572
NM_002878.3(RAD51D):c.263+1588A>G rs180869630
NM_002878.3(RAD51D):c.263+1641C>T rs142387263
NM_002878.3(RAD51D):c.26G>C (p.Cys9Ser) rs140825795
NM_002878.3(RAD51D):c.355T>C (p.Cys119Arg) rs201313861
NM_002878.3(RAD51D):c.363del (p.Ala122fs) rs730881935
NM_002878.3(RAD51D):c.401A>G (p.Tyr134Cys) rs1567728366
NM_002878.3(RAD51D):c.480+4A>G rs1567728211
NM_002878.3(RAD51D):c.481G>T (p.Ala161Ser) rs1567727951
NM_002878.3(RAD51D):c.493C>G (p.Arg165Gly) rs544654228
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.620C>T (p.Ser207Leu) rs370228071
NM_002878.3(RAD51D):c.694C>T (p.Arg232Ter) rs587780104
NM_002878.3(RAD51D):c.70A>G (p.Arg24Gly) rs781611267
NM_002878.3(RAD51D):c.715C>T (p.Arg239Trp) rs770250516
NM_002878.3(RAD51D):c.716G>A (p.Arg239Gln) rs780921112
NM_002878.3(RAD51D):c.748del (p.His250fs) rs587780105
NM_002878.3(RAD51D):c.793G>A (p.Gly265Arg) rs140285068
NM_002878.3(RAD51D):c.80C>A (p.Thr27Lys) rs139642328
NM_002878.3(RAD51D):c.80C>T (p.Thr27Ile) rs139642328
NM_002878.3(RAD51D):c.823C>T (p.Arg275Trp) rs752780416
NM_002878.3(RAD51D):c.83-3C>G rs1555570424
NM_002878.3(RAD51D):c.83-4T>A rs1567735916
NM_002878.3(RAD51D):c.839C>G (p.Thr280Ser) rs548111162
NM_002878.3(RAD51D):c.862G>C (p.Gly288Arg) rs1391505912
NM_002878.3(RAD51D):c.86T>C (p.Val29Ala) rs1567735899
NM_002878.3(RAD51D):c.898C>T (p.Arg300Ter) rs750621215
NM_002878.3(RAD51D):c.899G>A (p.Arg300Gln) rs761290755
NM_002878.3(RAD51D):c.904-3C>T rs45478491
NM_002878.3(RAD51D):c.919G>A (p.Glu307Lys) rs115031549
NM_002878.3(RAD51D):c.932T>A (p.Ile311Asn) rs145309168
NM_002878.3(RAD51D):c.973G>A (p.Gly325Ser) rs587780106
NM_002878.3(RAD51D):c.983C>T (p.Thr328Ile) rs138969595

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