ClinVar Miner

List of variants in gene combination RAD51D, RAD51L3-RFFL reported by Mendelics

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Total variants: 57
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HGVS dbSNP gnomAD frequency
NM_002878.4(RAD51D):c.568G>A (p.Ala190Thr) rs80116829 0.00167
NM_002878.4(RAD51D):c.263+1588A>G rs180869630 0.00123
NM_002878.4(RAD51D):c.146C>T (p.Ala49Val) rs140317560 0.00116
NM_002878.4(RAD51D):c.263+1509C>T rs201506572 0.00116
NM_002878.4(RAD51D):c.919G>A (p.Glu307Lys) rs115031549 0.00083
NM_002878.4(RAD51D):c.932T>A (p.Ile311Asn) rs145309168 0.00041
NM_002878.4(RAD51D):c.26G>C (p.Cys9Ser) rs140825795 0.00037
NM_002878.4(RAD51D):c.263+1605G>A rs147933658 0.00023
NM_002878.4(RAD51D):c.983C>T (p.Thr328Ile) rs138969595 0.00021
NM_002878.4(RAD51D):c.39C>G (p.Thr13=) rs146448657 0.00018
NM_002878.4(RAD51D):c.904-3C>T rs45478491 0.00018
NM_002878.4(RAD51D):c.137C>G (p.Ser46Cys) rs587780102 0.00010
NM_002878.4(RAD51D):c.355T>C (p.Cys119Arg) rs201313861 0.00008
NM_002878.4(RAD51D):c.973G>A (p.Gly325Ser) rs587780106 0.00008
NM_002878.4(RAD51D):c.263+1641C>T rs142387263 0.00006
NM_002878.4(RAD51D):c.263+7G>A rs56218020 0.00006
NM_002878.4(RAD51D):c.715C>T (p.Arg239Trp) rs770250516 0.00006
NM_002878.4(RAD51D):c.957G>A (p.Gln319=) rs147669627 0.00006
NM_002878.4(RAD51D):c.694C>T (p.Arg232Ter) rs587780104 0.00004
NM_002878.4(RAD51D):c.793G>A (p.Gly265Arg) rs140285068 0.00004
NM_002878.4(RAD51D):c.796C>T (p.Arg266Cys) rs587781813 0.00004
NM_002878.4(RAD51D):c.839C>G (p.Thr280Ser) rs548111162 0.00004
NM_002878.4(RAD51D):c.481-8C>T rs762247126 0.00003
NM_002878.4(RAD51D):c.556C>T (p.Arg186Ter) rs387906843 0.00003
NM_002878.4(RAD51D):c.83-37C>A rs763129236 0.00003
NM_002878.4(RAD51D):c.164G>A (p.Arg55Gln) rs151198586 0.00002
NM_002878.4(RAD51D):c.363del (p.Ala122fs) rs730881935 0.00002
NM_002878.4(RAD51D):c.898C>T (p.Arg300Ter) rs750621215 0.00002
NM_002878.4(RAD51D):c.899G>A (p.Arg300Gln) rs761290755 0.00002
NM_002878.4(RAD51D):c.263+1585C>G rs1192914615 0.00001
NM_002878.4(RAD51D):c.70A>G (p.Arg24Gly) rs781611267 0.00001
NM_002878.4(RAD51D):c.716G>A (p.Arg239Gln) rs780921112 0.00001
NM_002878.4(RAD51D):c.80C>A (p.Thr27Lys) rs139642328 0.00001
NM_002878.4(RAD51D):c.823C>T (p.Arg275Trp) rs752780416 0.00001
NM_002878.4(RAD51D):c.862G>C (p.Gly288Arg) rs1391505912 0.00001
NM_002878.4(RAD51D):c.900A>G (p.Arg300=) rs370634278 0.00001
NM_002878.4(RAD51D):c.109G>C (p.Glu37Gln) rs876659848
NM_002878.4(RAD51D):c.192C>T (p.Phe64=) rs1567735397
NM_002878.4(RAD51D):c.1A>G (p.Met1Val) rs561425038
NM_002878.4(RAD51D):c.232T>G (p.Ser78Ala) rs1567735315
NM_002878.4(RAD51D):c.263+1450T>A rs1567734484
NM_002878.4(RAD51D):c.263+1551G>T rs780006577
NM_002878.4(RAD51D):c.263+1644T>C rs1597874516
NM_002878.4(RAD51D):c.401A>G (p.Tyr134Cys) rs1567728366
NM_002878.4(RAD51D):c.475del (p.Glu159fs) rs1597862493
NM_002878.4(RAD51D):c.480+4A>G rs1567728211
NM_002878.4(RAD51D):c.481G>T (p.Ala161Ser) rs1567727951
NM_002878.4(RAD51D):c.493C>G (p.Arg165Gly) rs544654228
NM_002878.4(RAD51D):c.667+2_667+23del rs1597858626
NM_002878.4(RAD51D):c.736G>A (p.Val246Met) rs1597858213
NM_002878.4(RAD51D):c.738+10C>A rs777453585
NM_002878.4(RAD51D):c.80C>T (p.Thr27Ile) rs139642328
NM_002878.4(RAD51D):c.83-3C>G rs1555570424
NM_002878.4(RAD51D):c.83-4T>A rs1567735916
NM_002878.4(RAD51D):c.844G>A (p.Glu282Lys) rs1447892901
NM_002878.4(RAD51D):c.86T>C (p.Val29Ala) rs1567735899
NM_002878.4(RAD51D):c.883C>G (p.Leu295Val) rs752910287

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