ClinVar Miner

List of variants in gene combination RAD51D, RAD51L3-RFFL reported as likely benign for not provided

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Total variants: 72
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HGVS dbSNP gnomAD frequency
NM_002878.4(RAD51D):c.739-235G>A rs28363288 0.01947
NM_002878.4(RAD51D):c.577-211T>C rs28363281 0.01276
NM_002878.4(RAD51D):c.903+53C>T rs45496096 0.01225
NM_002878.4(RAD51D):c.698A>G (p.Glu233Gly) rs28363284 0.01102
NM_002878.4(RAD51D):c.903+61A>G rs9914109 0.01068
NM_002878.4(RAD51D):c.263+1816C>T rs145397692 0.00891
NM_002878.4(RAD51D):c.695G>A (p.Arg232Gln) rs28363283 0.00457
NM_002878.4(RAD51D):c.263+1323C>A rs28363263 0.00390
NM_002878.4(RAD51D):c.263+1855G>A rs139512155 0.00390
NM_002878.4(RAD51D):c.263+1857_263+1858insT rs558397245 0.00389
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.919G>A (p.Glu307Lys) rs115031549 0.00083
NM_002878.4(RAD51D):c.932T>A (p.Ile311Asn) rs145309168 0.00041
NM_002878.4(RAD51D):c.904-11T>A rs374449943 0.00038
NM_002878.4(RAD51D):c.26G>C (p.Cys9Ser) rs140825795 0.00037
NM_002878.4(RAD51D):c.216C>T (p.Tyr72=) rs148690585 0.00028
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.145-40C>T rs370850037 0.00011
NM_002878.4(RAD51D):c.196G>A (p.Val66Met) rs56026142 0.00009
NM_002878.4(RAD51D):c.864C>T (p.Gly288=) rs138557828 0.00009
NM_002878.4(RAD51D):c.145-4G>A rs201361465 0.00006
NM_002878.4(RAD51D):c.263+7G>A rs56218020 0.00006
NM_002878.4(RAD51D):c.957G>A (p.Gln319=) rs147669627 0.00006
NM_002878.4(RAD51D):c.346-10C>T rs779972784 0.00005
NM_002878.4(RAD51D):c.145-13G>T rs760867838 0.00004
NM_002878.4(RAD51D):c.264-7C>T rs753529790 0.00004
NM_002878.4(RAD51D):c.667+20C>T rs373473666 0.00004
NM_002878.4(RAD51D):c.195C>T (p.Pro65=) rs376616485 0.00003
NM_002878.4(RAD51D):c.481-8C>T rs762247126 0.00003
NM_002878.4(RAD51D):c.765G>A (p.Arg255=) rs751833940 0.00003
NM_002878.4(RAD51D):c.879G>A (p.Ala293=) rs368209468 0.00003
NM_002878.4(RAD51D):c.171G>A (p.Leu57=) rs786202885 0.00002
NM_002878.4(RAD51D):c.393C>T (p.Asn131=) rs772605790 0.00002
NM_002878.4(RAD51D):c.966A>G (p.Thr322=) rs786203299 0.00002
NM_002878.4(RAD51D):c.12C>G (p.Leu4=) rs786203193 0.00001
NM_002878.4(RAD51D):c.198G>T (p.Val66=) rs200810304 0.00001
NM_002878.4(RAD51D):c.27C>T (p.Cys9=) rs200487648 0.00001
NM_002878.4(RAD51D):c.333C>T (p.Ser111=) rs369396909 0.00001
NM_002878.4(RAD51D):c.345+5A>G rs878854562 0.00001
NM_002878.4(RAD51D):c.481-11C>T rs372690151 0.00001
NM_002878.4(RAD51D):c.510G>A (p.Val170=) rs142134504 0.00001
NM_002878.4(RAD51D):c.576+19C>T rs749835057 0.00001
NM_002878.4(RAD51D):c.577-13C>A rs748697766 0.00001
NM_002878.4(RAD51D):c.621G>T (p.Ser207=) rs749859221 0.00001
NM_002878.4(RAD51D):c.900A>G (p.Arg300=) rs370634278 0.00001
NM_002878.4(RAD51D):c.145-39G>T rs7207508
NM_002878.4(RAD51D):c.163C>T (p.Arg55Trp) rs775268017
NM_002878.4(RAD51D):c.223C>T (p.Leu75=) rs746929682
NM_002878.4(RAD51D):c.231C>G (p.Thr77=) rs376670250
NM_002878.4(RAD51D):c.263+1631C>T
NM_002878.4(RAD51D):c.294T>C (p.Tyr98=)
NM_002878.4(RAD51D):c.33C>T (p.Gly11=) rs760444811
NM_002878.4(RAD51D):c.412A>C (p.Asn138His) rs141690729
NM_002878.4(RAD51D):c.426A>G (p.Thr142=) rs1597862600
NM_002878.4(RAD51D):c.456T>C (p.Ala152=) rs921214343
NM_002878.4(RAD51D):c.481-4T>G rs876659339
NM_002878.4(RAD51D):c.570C>T (p.Ala190=) rs750479232
NM_002878.4(RAD51D):c.621G>A (p.Ser207=) rs749859221
NM_002878.4(RAD51D):c.667+3G>A rs773138393
NM_002878.4(RAD51D):c.668-4G>T rs1001440122
NM_002878.4(RAD51D):c.66C>T (p.Ser22=) rs876660902
NM_002878.4(RAD51D):c.708C>T (p.Thr236=)
NM_002878.4(RAD51D):c.757C>A (p.Arg253=) rs137886232
NM_002878.4(RAD51D):c.82+128C>T rs28363258
NM_002878.4(RAD51D):c.82+5_82+12del rs1597878477
NM_002878.4(RAD51D):c.834G>A (p.Leu278=) rs876658123
NM_002878.4(RAD51D):c.849A>C (p.Gly283=) rs766847072
NM_002878.4(RAD51D):c.879G>C (p.Ala293=) rs368209468

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