ClinVar Miner

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

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 133
Download table as spreadsheet
HGVS dbSNP
NM_002878.3(RAD51D):c.*10T>A rs759502122
NM_002878.3(RAD51D):c.*7C>T rs370985675
NM_002878.3(RAD51D):c.-7G>C rs553444507
NM_002878.3(RAD51D):c.108G>A (p.Leu36=) rs755962971
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.132C>T (p.Gly44=) rs761651126
NM_002878.3(RAD51D):c.144+17C>G rs1567735764
NM_002878.3(RAD51D):c.144+17C>T rs1567735764
NM_002878.3(RAD51D):c.145-11C>A rs773851850
NM_002878.3(RAD51D):c.145-13G>T rs760867838
NM_002878.3(RAD51D):c.145-14G>C rs200470533
NM_002878.3(RAD51D):c.145-18T>C rs1567735483
NM_002878.3(RAD51D):c.145-20A>G rs759639583
NM_002878.3(RAD51D):c.145-3C>T rs201974522
NM_002878.3(RAD51D):c.145-4G>A rs201361465
NM_002878.3(RAD51D):c.171G>A (p.Leu57=) rs786202885
NM_002878.3(RAD51D):c.177T>C (p.Ala59=) rs1567735421
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.216C>T (p.Tyr72=) rs148690585
NM_002878.3(RAD51D):c.255C>T (p.Gly85=) rs750714062
NM_002878.3(RAD51D):c.263+1455delA rs979233150
NM_002878.3(RAD51D):c.263+1474C>T rs201720876
NM_002878.3(RAD51D):c.263+1478C>T rs200538950
NM_002878.3(RAD51D):c.263+1578G>A rs1391871647
NM_002878.3(RAD51D):c.263+1588A>G rs180869630
NM_002878.3(RAD51D):c.263+1596_263+1597insT rs1335185570
NM_002878.3(RAD51D):c.263+1605G>A rs147933658
NM_002878.3(RAD51D):c.263+1618G>A rs748411608
NM_002878.3(RAD51D):c.263+1621G>C rs1310166106
NM_002878.3(RAD51D):c.263+18G>A rs1567735210
NM_002878.3(RAD51D):c.263+7G>A rs56218020
NM_002878.3(RAD51D):c.264-14delT rs757481281
NM_002878.3(RAD51D):c.264-5A>T rs1169894160
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.324C>T (p.Gly108=) rs758132417
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.345+14C>T rs1567728611
NM_002878.3(RAD51D):c.345+17C>T rs760529001
NM_002878.3(RAD51D):c.345+18A>T rs1555568465
NM_002878.3(RAD51D):c.345+6T>C rs1555568466
NM_002878.3(RAD51D):c.346-10C>T rs779972784
NM_002878.3(RAD51D):c.346-16A>G rs749176675
NM_002878.3(RAD51D):c.346-19C>T rs1567728479
NM_002878.3(RAD51D):c.346-4C>G rs767328693
NM_002878.3(RAD51D):c.346-7C>T rs1060504768
NM_002878.3(RAD51D):c.355T>C (p.Cys119Arg) rs201313861
NM_002878.3(RAD51D):c.357T>C (p.Cys119=) rs1272809785
NM_002878.3(RAD51D):c.381C>G (p.Gly127=) rs1555568350
NM_002878.3(RAD51D):c.382C>T (p.Leu128=) rs1438461174
NM_002878.3(RAD51D):c.384G>A (p.Leu128=) rs1393403501
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.408T>C (p.Asp136=) rs1567728349
NM_002878.3(RAD51D):c.413A>G (p.Asn138Ser) rs201676898
NM_002878.3(RAD51D):c.420G>T (p.Gly140=) rs1567728317
NM_002878.3(RAD51D):c.480+18G>C rs1435211888
NM_002878.3(RAD51D):c.480+6G>A rs1057523143
NM_002878.3(RAD51D):c.481-11C>T rs372690151
NM_002878.3(RAD51D):c.481-23_481-20delGCTT rs760861758
NM_002878.3(RAD51D):c.481-7G>A rs145832514
NM_002878.3(RAD51D):c.481-8C>T rs762247126
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.576+12G>A rs757751100
NM_002878.3(RAD51D):c.576+18C>T rs752051995
NM_002878.3(RAD51D):c.576+19C>T rs749835057
NM_002878.3(RAD51D):c.577-13C>A rs748697766
NM_002878.3(RAD51D):c.577-7C>T rs1438561890
NM_002878.3(RAD51D):c.582T>C (p.Thr194=) rs1555567645
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.657G>A (p.Gln219=) rs1567726462
NM_002878.3(RAD51D):c.667+20C>T rs373473666
NM_002878.3(RAD51D):c.667+24G>A rs371610084
NM_002878.3(RAD51D):c.667+9T>C rs772193051
NM_002878.3(RAD51D):c.668-7_668-5delCCT rs1230625396
NM_002878.3(RAD51D):c.669C>G (p.Gly223=) rs1567726315
NM_002878.3(RAD51D):c.66C>T (p.Ser22=) rs876660902
NM_002878.3(RAD51D):c.675C>T (p.Ala225=) rs760789270
NM_002878.3(RAD51D):c.699G>A (p.Glu233=) rs1555567518
NM_002878.3(RAD51D):c.714C>T (p.Ala238=) rs780258990
NM_002878.3(RAD51D):c.715C>T (p.Arg239Trp) rs770250516
NM_002878.3(RAD51D):c.720C>T (p.Asp240=) rs1555567499
NM_002878.3(RAD51D):c.738+11A>G rs758241019
NM_002878.3(RAD51D):c.738+13G>T rs752733014
NM_002878.3(RAD51D):c.738+14C>T rs374761868
NM_002878.3(RAD51D):c.738+17G>A rs753635983
NM_002878.3(RAD51D):c.739-10T>C rs199998187
NM_002878.3(RAD51D):c.739-17G>T rs1567725135
NM_002878.3(RAD51D):c.739-3C>T rs1235042092
NM_002878.3(RAD51D):c.757C>A (p.Arg253=) rs137886232
NM_002878.3(RAD51D):c.759A>C (p.Arg253=) rs1555567179
NM_002878.3(RAD51D):c.765G>A (p.Arg255=) rs751833940
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.82+15G>A rs778216370
NM_002878.3(RAD51D):c.82+16C>T rs1555570476
NM_002878.3(RAD51D):c.82+9G>A rs747267285
NM_002878.3(RAD51D):c.83-20T>C rs182793287
NM_002878.3(RAD51D):c.83-26A>G rs202048781
NM_002878.3(RAD51D):c.83-4T>C rs1567735916
NM_002878.3(RAD51D):c.83-8G>C rs1567735932
NM_002878.3(RAD51D):c.83-8delG rs1555570426
NM_002878.3(RAD51D):c.849A>C (p.Gly283=) rs766847072
NM_002878.3(RAD51D):c.864C>T (p.Gly288=) rs138557828
NM_002878.3(RAD51D):c.869G>A (p.Arg290Gln) rs773883374
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.888C>G (p.Ala296=) rs755177638
NM_002878.3(RAD51D):c.900A>G (p.Arg300=) rs370634278
NM_002878.3(RAD51D):c.904-11T>A rs374449943
NM_002878.3(RAD51D):c.904-14_904-11delACTT rs1357935702
NM_002878.3(RAD51D):c.904-3C>T rs45478491
NM_002878.3(RAD51D):c.904-6_904-4delTTC rs779850240
NM_002878.3(RAD51D):c.904-9T>G rs1555567012
NM_002878.3(RAD51D):c.90C>T (p.Asp30=) rs374725981
NM_002878.3(RAD51D):c.915C>G (p.Phe305Leu) rs1316114457
NM_002878.3(RAD51D):c.922A>G (p.Met308Val) rs786201961
NM_002878.3(RAD51D):c.939C>A (p.Thr313=) rs374318553
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

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.