ClinVar Miner

List of variants in gene combination RAD51D, RAD51L3-RFFL reported as likely benign by Ambry Genetics

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Gene type:
ClinVar version:
Total variants: 84
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HGVS dbSNP
NM_002878.3(RAD51D):c.108G>A (p.Leu36=) rs755962971
NM_002878.3(RAD51D):c.117A>T (p.Val39=) rs876660008
NM_002878.3(RAD51D):c.126A>G (p.Lys42=) rs145361433
NM_002878.3(RAD51D):c.12C>G (p.Leu4=) rs786203193
NM_002878.3(RAD51D):c.144+3G>T rs761057565
NM_002878.3(RAD51D):c.145-4G>A rs201361465
NM_002878.3(RAD51D):c.146C>T (p.Ala49Val) rs140317560
NM_002878.3(RAD51D):c.163C>A (p.Arg55=) rs775268017
NM_002878.3(RAD51D):c.171G>A (p.Leu57=) rs786202885
NM_002878.3(RAD51D):c.183C>T (p.Phe61=) rs1185842552
NM_002878.3(RAD51D):c.186G>A (p.Ser62=) rs746984258
NM_002878.3(RAD51D):c.195C>T (p.Pro65=) rs376616485
NM_002878.3(RAD51D):c.196G>A (p.Val66Met) rs56026142
NM_002878.3(RAD51D):c.198G>T (p.Val66=) rs200810304
NM_002878.3(RAD51D):c.204C>A (p.Gly68=) rs764351040
NM_002878.3(RAD51D):c.204C>T (p.Gly68=) rs764351040
NM_002878.3(RAD51D):c.213C>T (p.Leu71=) rs745546403
NM_002878.3(RAD51D):c.216C>T (p.Tyr72=) rs148690585
NM_002878.3(RAD51D):c.223C>T (p.Leu75=) rs746929682
NM_002878.3(RAD51D):c.231C>G (p.Thr77=) rs376670250
NM_002878.3(RAD51D):c.255C>T (p.Gly85=) rs750714062
NM_002878.3(RAD51D):c.27C>T (p.Cys9=) rs200487648
NM_002878.3(RAD51D):c.333C>T (p.Ser111=) rs369396909
NM_002878.3(RAD51D):c.33C>T (p.Gly11=) rs760444811
NM_002878.3(RAD51D):c.393C>T (p.Asn131=) rs772605790
NM_002878.3(RAD51D):c.394G>A (p.Val132Ile) rs201141245
NM_002878.3(RAD51D):c.396C>T (p.Val132=) rs1555568341
NM_002878.3(RAD51D):c.39C>G (p.Thr13=) rs146448657
NM_002878.3(RAD51D):c.39C>T (p.Thr13=) rs146448657
NM_002878.3(RAD51D):c.413A>G (p.Asn138Ser) rs201676898
NM_002878.3(RAD51D):c.414T>C (p.Asn138=) rs1555568320
NM_002878.3(RAD51D):c.417A>C (p.Gly139=) rs786202049
NM_002878.3(RAD51D):c.438C>T (p.Leu146=) rs145452047
NM_002878.3(RAD51D):c.471G>A (p.Glu157=) rs55942401
NM_002878.3(RAD51D):c.507G>A (p.Val169=) rs1555568162
NM_002878.3(RAD51D):c.510G>A (p.Val170=) rs142134504
NM_002878.3(RAD51D):c.51C>T (p.Ile17=) rs769903986
NM_002878.3(RAD51D):c.537G>A (p.Leu179=) rs1555568141
NM_002878.3(RAD51D):c.543G>A (p.Val181=) rs1555568135
NM_002878.3(RAD51D):c.568G>A (p.Ala190Thr) rs80116829
NM_002878.3(RAD51D):c.570C>T (p.Ala190=) rs750479232
NM_002878.3(RAD51D):c.606G>C (p.Val202=) rs1555567627
NM_002878.3(RAD51D):c.609G>T (p.Val203=) rs876660256
NM_002878.3(RAD51D):c.610G>A (p.Val204Ile) rs765881830
NM_002878.3(RAD51D):c.621G>A (p.Ser207=) rs749859221
NM_002878.3(RAD51D):c.621G>T (p.Ser207=) rs749859221
NM_002878.3(RAD51D):c.627T>C (p.Thr209=) rs141545966
NM_002878.3(RAD51D):c.630G>A (p.Ala210=) rs762585552
NM_002878.3(RAD51D):c.642A>G (p.Pro214=) rs876660847
NM_002878.3(RAD51D):c.663G>A (p.Arg221=) rs876660896
NM_002878.3(RAD51D):c.666A>G (p.Glu222=) rs114012742
NM_002878.3(RAD51D):c.66C>T (p.Ser22=) rs876660902
NM_002878.3(RAD51D):c.68A>G (p.His23Arg) rs990062370
NM_002878.3(RAD51D):c.690G>A (p.Leu230=) rs1555567526
NM_002878.3(RAD51D):c.726C>T (p.Gly242=) rs1555567496
NM_002878.3(RAD51D):c.757C>A (p.Arg253=) rs137886232
NM_002878.3(RAD51D):c.75C>T (p.Ile25=) rs1555570482
NM_002878.3(RAD51D):c.765G>A (p.Arg255=) rs751833940
NM_002878.3(RAD51D):c.771C>T (p.Ser257=) rs146212490
NM_002878.3(RAD51D):c.780C>A (p.Leu260=) rs772985579
NM_002878.3(RAD51D):c.786T>C (p.Pro262=) rs771631684
NM_002878.3(RAD51D):c.792C>T (p.Leu264=) rs536544621
NM_002878.3(RAD51D):c.823C>A (p.Arg275=) rs752780416
NM_002878.3(RAD51D):c.834G>A (p.Leu278=) rs876658123
NM_002878.3(RAD51D):c.840C>T (p.Thr280=) rs751885496
NM_002878.3(RAD51D):c.843C>T (p.Ile281=) rs754455433
NM_002878.3(RAD51D):c.864C>T (p.Gly288=) rs138557828
NM_002878.3(RAD51D):c.865G>A (p.Gly289Ser) rs587782129
NM_002878.3(RAD51D):c.869G>A (p.Arg290Gln) rs773883374
NM_002878.3(RAD51D):c.873C>T (p.Arg291=) rs140848654
NM_002878.3(RAD51D):c.878C>T (p.Ala293Val) rs769732230
NM_002878.3(RAD51D):c.879G>A (p.Ala293=) rs368209468
NM_002878.3(RAD51D):c.879G>C (p.Ala293=) rs368209468
NM_002878.3(RAD51D):c.879G>T (p.Ala293=) rs368209468
NM_002878.3(RAD51D):c.885G>A (p.Leu295=) rs876659714
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.922A>G (p.Met308Val) rs786201961
NM_002878.3(RAD51D):c.945G>A (p.Gly315=) rs142316409
NM_002878.3(RAD51D):c.954G>A (p.Glu318=) rs876658131
NM_002878.3(RAD51D):c.957G>A (p.Gln319=) rs147669627
NM_002878.3(RAD51D):c.966A>G (p.Thr322=) rs786203299
NM_002878.3(RAD51D):c.983C>T (p.Thr328Ile) rs138969595

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