ClinVar Miner

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

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Gene type:
ClinVar version:
Total variants: 97
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HGVS dbSNP
NM_002878.3(RAD51D):c.*12_*14delGTT rs745601646
NM_002878.3(RAD51D):c.*4G>A rs876659026
NM_002878.3(RAD51D):c.-10T>G rs746408351
NM_002878.3(RAD51D):c.-22G>A rs756566632
NM_002878.3(RAD51D):c.-27C>A rs1057521550
NM_002878.3(RAD51D):c.-27C>T rs1057521550
NM_002878.3(RAD51D):c.-28C>T rs375452513
NM_002878.3(RAD51D):c.-34A>G rs372716334
NM_002878.3(RAD51D):c.-43G>A rs776435937
NM_002878.3(RAD51D):c.-48C>A rs759556682
NM_002878.3(RAD51D):c.-48C>T rs759556682
NM_002878.3(RAD51D):c.-7G>T rs553444507
NM_002878.3(RAD51D):c.12C>G (p.Leu4=) rs786203193
NM_002878.3(RAD51D):c.145-13G>T rs760867838
NM_002878.3(RAD51D):c.145-16_145-15delTG rs1555570314
NM_002878.3(RAD51D):c.145-20A>G rs759639583
NM_002878.3(RAD51D):c.145-4G>A rs201361465
NM_002878.3(RAD51D):c.145-4G>T rs201361465
NM_002878.3(RAD51D):c.146C>T (p.Ala49Val) rs140317560
NM_002878.3(RAD51D):c.171G>A (p.Leu57=) rs786202885
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.223C>T (p.Leu75=) rs746929682
NM_002878.3(RAD51D):c.263+1323C>A
NM_002878.3(RAD51D):c.263+1816C>T
NM_002878.3(RAD51D):c.263+1855G>A
NM_002878.3(RAD51D):c.263+1857_263+1858insT
NM_002878.3(RAD51D):c.263+20delG rs1555570237
NM_002878.3(RAD51D):c.263+7G>A rs56218020
NM_002878.3(RAD51D):c.263+9G>C rs887322398
NM_002878.3(RAD51D):c.264-14delT rs757481281
NM_002878.3(RAD51D):c.264-15C>G rs56103933
NM_002878.3(RAD51D):c.264-4T>C rs1057523781
NM_002878.3(RAD51D):c.264-7C>T rs753529790
NM_002878.3(RAD51D):c.276G>C (p.Leu92=) rs1057522424
NM_002878.3(RAD51D):c.27C>T (p.Cys9=) rs200487648
NM_002878.3(RAD51D):c.300A>C (p.Gly100=) rs1555568499
NM_002878.3(RAD51D):c.309T>C (p.Thr103=) rs1057524665
NM_002878.3(RAD51D):c.324C>T (p.Gly108=) rs758132417
NM_002878.3(RAD51D):c.333C>T (p.Ser111=) rs369396909
NM_002878.3(RAD51D):c.345+5A>G rs878854562
NM_002878.3(RAD51D):c.345+5A>T rs878854562
NM_002878.3(RAD51D):c.346-16A>G rs749176675
NM_002878.3(RAD51D):c.384G>T (p.Leu128=) rs1393403501
NM_002878.3(RAD51D):c.393C>T (p.Asn131=) rs772605790
NM_002878.3(RAD51D):c.39C>G (p.Thr13=) rs146448657
NM_002878.3(RAD51D):c.405A>G (p.Val135=) rs1555568330
NM_002878.3(RAD51D):c.421C>T (p.Leu141=) rs1057523780
NM_002878.3(RAD51D):c.480+6G>A rs1057523143
NM_002878.3(RAD51D):c.481-11C>T rs372690151
NM_002878.3(RAD51D):c.481-4T>G rs876659339
NM_002878.3(RAD51D):c.481-5T>G rs374382703
NM_002878.3(RAD51D):c.481-8C>T rs762247126
NM_002878.3(RAD51D):c.510G>A (p.Val170=) rs142134504
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.576+12G>A rs757751100
NM_002878.3(RAD51D):c.576+12G>C rs757751100
NM_002878.3(RAD51D):c.576+19C>T rs749835057
NM_002878.3(RAD51D):c.577-13C>A rs748697766
NM_002878.3(RAD51D):c.577-17C>G rs758865282
NM_002878.3(RAD51D):c.577-211T>C
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.630G>A (p.Ala210=) rs762585552
NM_002878.3(RAD51D):c.654T>A (p.Gly218=) rs1057521173
NM_002878.3(RAD51D):c.663G>A (p.Arg221=) rs876660896
NM_002878.3(RAD51D):c.667+20C>T rs373473666
NM_002878.3(RAD51D):c.667+8A>T rs941079937
NM_002878.3(RAD51D):c.668-4G>A rs1001440122
NM_002878.3(RAD51D):c.668-4G>T rs1001440122
NM_002878.3(RAD51D):c.668-7_668-5delCCT rs1230625396
NM_002878.3(RAD51D):c.6C>T (p.Gly2=) rs1255954226
NM_002878.3(RAD51D):c.738+11A>G rs758241019
NM_002878.3(RAD51D):c.738+13G>T rs752733014
NM_002878.3(RAD51D):c.738+17G>A rs753635983
NM_002878.3(RAD51D):c.738+3G>A rs751062153
NM_002878.3(RAD51D):c.739-4G>T rs1555567205
NM_002878.3(RAD51D):c.757C>A (p.Arg253=) rs137886232
NM_002878.3(RAD51D):c.765G>A (p.Arg255=) rs751833940
NM_002878.3(RAD51D):c.768C>T (p.Asp256=) rs569428131
NM_002878.3(RAD51D):c.786T>C (p.Pro262=) rs771631684
NM_002878.3(RAD51D):c.789C>T (p.Ala263=) rs1555567153
NM_002878.3(RAD51D):c.82+128C>T
NM_002878.3(RAD51D):c.82+5_82+12delCCGGGTGT
NM_002878.3(RAD51D):c.83-19A>G rs1057523591
NM_002878.3(RAD51D):c.834G>A (p.Leu278=) rs876658123
NM_002878.3(RAD51D):c.879G>A (p.Ala293=) rs368209468
NM_002878.3(RAD51D):c.900A>G (p.Arg300=) rs370634278
NM_002878.3(RAD51D):c.903+53C>T
NM_002878.3(RAD51D):c.904-11T>A rs374449943
NM_002878.3(RAD51D):c.904-17C>T rs181816960
NM_002878.3(RAD51D):c.921G>A (p.Glu307=) rs1057523377
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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