ClinVar Miner

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

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Total variants: 72
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HGVS dbSNP
NM_002878.3(RAD51D):c.-238A>T rs188262287
NM_002878.3(RAD51D):c.-99T>C rs533209845
NM_002878.3(RAD51D):c.131G>A (p.Gly44Asp) rs374730714
NM_002878.3(RAD51D):c.137C>G (p.Ser46Cys) rs587780102
NM_002878.3(RAD51D):c.145-13G>T rs760867838
NM_002878.3(RAD51D):c.145-14G>C rs200470533
NM_002878.3(RAD51D):c.145-4G>A rs201361465
NM_002878.3(RAD51D):c.146C>T (p.Ala49Val) rs140317560
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.1A>G (p.Met1Val) rs561425038
NM_002878.3(RAD51D):c.1A>T (p.Met1Leu) rs561425038
NM_002878.3(RAD51D):c.216C>T (p.Tyr72=) rs148690585
NM_002878.3(RAD51D):c.234C>T (p.Ser78=) rs9901455
NM_002878.3(RAD51D):c.263+1455delA rs979233150
NM_002878.3(RAD51D):c.263+1507_263+1509delTGC rs753760360
NM_002878.3(RAD51D):c.263+1509C>T rs201506572
NM_002878.3(RAD51D):c.263+1570T>A rs376472075
NM_002878.3(RAD51D):c.263+1588A>G rs180869630
NM_002878.3(RAD51D):c.263+1596T>C rs1057517631
NM_002878.3(RAD51D):c.263+1597C>A rs755753106
NM_002878.3(RAD51D):c.263+1605G>A rs147933658
NM_002878.3(RAD51D):c.263+1612delA rs750282687
NM_002878.3(RAD51D):c.263+1627C>T rs188981311
NM_002878.3(RAD51D):c.263+7G>A rs56218020
NM_002878.3(RAD51D):c.264-14delT rs757481281
NM_002878.3(RAD51D):c.26G>C (p.Cys9Ser) rs140825795
NM_002878.3(RAD51D):c.270_271dup (p.Lys91fs) rs753862052
NM_002878.3(RAD51D):c.286G>T (p.Gly96Cys) rs762951311
NM_002878.3(RAD51D):c.326dup (p.Gly110fs) rs730882119
NM_002878.3(RAD51D):c.339A>C (p.Lys113Asn) rs786202507
NM_002878.3(RAD51D):c.349T>A (p.Cys117Ser) rs786201358
NM_002878.3(RAD51D):c.363del (p.Ala122fs) rs730881935
NM_002878.3(RAD51D):c.394G>A (p.Val132Ile) rs201141245
NM_002878.3(RAD51D):c.413A>G (p.Asn138Ser) rs201676898
NM_002878.3(RAD51D):c.433C>T (p.Arg145Cys) rs755173206
NM_002878.3(RAD51D):c.451C>T (p.Gln151Ter) rs587781756
NM_002878.3(RAD51D):c.478C>T (p.Gln160Ter) rs1057521922
NM_002878.3(RAD51D):c.481-7G>A rs145832514
NM_002878.3(RAD51D):c.481-8C>T rs762247126
NM_002878.3(RAD51D):c.494G>A (p.Arg165Gln) rs4796033
NM_002878.3(RAD51D):c.53A>G (p.Gln18Arg) rs546225564
NM_002878.3(RAD51D):c.556C>T (p.Arg186Ter) rs387906843
NM_002878.3(RAD51D):c.568G>A (p.Ala190Thr) rs80116829
NM_002878.3(RAD51D):c.576+1G>A rs781161543
NM_002878.3(RAD51D):c.620C>T (p.Ser207Leu) rs370228071
NM_002878.3(RAD51D):c.629C>T (p.Ala210Val) rs376855484
NM_002878.3(RAD51D):c.649G>T (p.Gly217Ter) rs775365939
NM_002878.3(RAD51D):c.655C>T (p.Gln219Ter) rs771007945
NM_002878.3(RAD51D):c.666A>G (p.Glu222=) rs114012742
NM_002878.3(RAD51D):c.694C>T (p.Arg232Ter) rs587780104
NM_002878.3(RAD51D):c.695G>A (p.Arg232Gln) rs28363283
NM_002878.3(RAD51D):c.698A>G (p.Glu233Gly) rs28363284
NM_002878.3(RAD51D):c.6_13dup (p.Arg5fs) rs1555570506
NM_002878.3(RAD51D):c.715C>T (p.Arg239Trp) rs770250516
NM_002878.3(RAD51D):c.716G>A (p.Arg239Gln) rs780921112
NM_002878.3(RAD51D):c.739-10T>C rs199998187
NM_002878.3(RAD51D):c.739-3C>T rs1235042092
NM_002878.3(RAD51D):c.740_741dup (p.Thr248Ter) rs1555567197
NM_002878.3(RAD51D):c.757C>A (p.Arg253=) rs137886232
NM_002878.3(RAD51D):c.757C>T (p.Arg253Ter) rs137886232
NM_002878.3(RAD51D):c.771C>T (p.Ser257=) rs146212490
NM_002878.3(RAD51D):c.785C>T (p.Pro262Leu) rs730881950
NM_002878.3(RAD51D):c.796C>T (p.Arg266Cys) rs587781813
NM_002878.3(RAD51D):c.81del (p.Val28fs) rs1064793952
NM_002878.3(RAD51D):c.85del (p.Val29fs) rs1057517586
NM_002878.3(RAD51D):c.873C>T (p.Arg291=) rs140848654
NM_002878.3(RAD51D):c.904-11T>A rs374449943
NM_002878.3(RAD51D):c.904-3C>T rs45478491
NM_002878.3(RAD51D):c.932T>A (p.Ile311Asn) rs145309168
NM_002878.3(RAD51D):c.94_95del (p.Val32fs) rs786203137
NM_002878.3(RAD51D):c.983C>T (p.Thr328Ile) rs138969595

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