ClinVar Miner

List of variants in gene combination RAD51D, RAD51L3-RFFL reported as uncertain significance by GeneDx

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Total variants: 74
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HGVS dbSNP
NM_002878.3(RAD51D):c.131G>A (p.Gly44Asp) rs374730714
NM_002878.3(RAD51D):c.131G>C (p.Gly44Ala) rs374730714
NM_002878.3(RAD51D):c.137C>G (p.Ser46Cys) rs587780102
NM_002878.3(RAD51D):c.145-12G>A rs1064795057
NM_002878.3(RAD51D):c.145-7T>A rs1064793407
NM_002878.3(RAD51D):c.164G>A (p.Arg55Gln) rs151198586
NM_002878.3(RAD51D):c.185C>T (p.Ser62Leu) rs374357106
NM_002878.3(RAD51D):c.196G>T (p.Val66Leu) rs56026142
NM_002878.3(RAD51D):c.19G>C (p.Gly7Arg) rs1064795913
NM_002878.3(RAD51D):c.205G>A (p.Ala69Thr) rs763439048
NM_002878.3(RAD51D):c.208G>A (p.Asp70Asn) rs142189122
NM_002878.3(RAD51D):c.263+20G>T rs763380219
NM_002878.3(RAD51D):c.26G>C (p.Cys9Ser) rs140825795
NM_002878.3(RAD51D):c.292T>A (p.Tyr98Asn) rs730881946
NM_002878.3(RAD51D):c.295A>G (p.Thr99Ala) rs746416079
NM_002878.3(RAD51D):c.329G>A (p.Gly110Asp) rs587780103
NM_002878.3(RAD51D):c.349T>A (p.Cys117Ser) rs786201358
NM_002878.3(RAD51D):c.355T>C (p.Cys119Arg) rs201313861
NM_002878.3(RAD51D):c.377A>T (p.His126Leu) rs144603589
NM_002878.3(RAD51D):c.38C>T (p.Thr13Ile) rs1064795830
NM_002878.3(RAD51D):c.394G>A (p.Val132Ile) rs201141245
NM_002878.3(RAD51D):c.407A>G (p.Asp136Gly) rs768197423
NM_002878.3(RAD51D):c.412A>C (p.Asn138His) rs141690729
NM_002878.3(RAD51D):c.412A>G (p.Asn138Asp) rs141690729
NM_002878.3(RAD51D):c.413A>G (p.Asn138Ser) rs201676898
NM_002878.3(RAD51D):c.419G>A (p.Gly140Glu) rs730881945
NM_002878.3(RAD51D):c.431C>T (p.Ser144Phe) rs587781875
NM_002878.3(RAD51D):c.434G>A (p.Arg145His) rs147264215
NM_002878.3(RAD51D):c.493C>G (p.Arg165Gly) rs544654228
NM_002878.3(RAD51D):c.493C>T (p.Arg165Trp) rs544654228
NM_002878.3(RAD51D):c.496A>G (p.Arg166Gly) rs1064793246
NM_002878.3(RAD51D):c.4G>A (p.Gly2Ser) rs372082751
NM_002878.3(RAD51D):c.4G>T (p.Gly2Cys) rs372082751
NM_002878.3(RAD51D):c.509T>C (p.Val170Ala) rs370679685
NM_002878.3(RAD51D):c.527T>C (p.Phe176Ser) rs1064794153
NM_002878.3(RAD51D):c.541G>A (p.Val181Met) rs876658678
NM_002878.3(RAD51D):c.603_605GGT[2] (p.Val205del) rs730881944
NM_002878.3(RAD51D):c.607G>A (p.Val203Met) rs730881947
NM_002878.3(RAD51D):c.623T>C (p.Val208Ala) rs1064795673
NM_002878.3(RAD51D):c.629C>A (p.Ala210Glu) rs376855484
NM_002878.3(RAD51D):c.629C>T (p.Ala210Val) rs376855484
NM_002878.3(RAD51D):c.634G>A (p.Val212Ile) rs730881948
NM_002878.3(RAD51D):c.667G>A (p.Gly223Ser) rs1064793247
NM_002878.3(RAD51D):c.668G>C (p.Gly223Ala) rs1064793588
NM_002878.3(RAD51D):c.68A>G (p.His23Arg) rs990062370
NM_002878.3(RAD51D):c.715C>T (p.Arg239Trp) rs770250516
NM_002878.3(RAD51D):c.745A>G (p.Asn249Asp) rs730881949
NM_002878.3(RAD51D):c.751A>G (p.Ile251Val) rs540273429
NM_002878.3(RAD51D):c.752T>A (p.Ile251Lys) rs778847822
NM_002878.3(RAD51D):c.767A>C (p.Asp256Ala) rs371350110
NM_002878.3(RAD51D):c.785C>T (p.Pro262Leu) rs730881950
NM_002878.3(RAD51D):c.793G>A (p.Gly265Arg) rs140285068
NM_002878.3(RAD51D):c.796C>T (p.Arg266Cys) rs587781813
NM_002878.3(RAD51D):c.797G>A (p.Arg266His) rs779808083
NM_002878.3(RAD51D):c.800C>T (p.Ser267Phe) rs1064793702
NM_002878.3(RAD51D):c.802T>A (p.Trp268Arg) rs755965977
NM_002878.3(RAD51D):c.821C>T (p.Thr274Ile) rs730881951
NM_002878.3(RAD51D):c.823C>T (p.Arg275Trp) rs752780416
NM_002878.3(RAD51D):c.824G>A (p.Arg275Gln) rs368914740
NM_002878.3(RAD51D):c.835G>A (p.Asp279Asn) rs765271127
NM_002878.3(RAD51D):c.865G>A (p.Gly289Ser) rs587782129
NM_002878.3(RAD51D):c.868C>T (p.Arg290Trp) rs527964137
NM_002878.3(RAD51D):c.869G>A (p.Arg290Gln) rs773883374
NM_002878.3(RAD51D):c.872G>A (p.Arg291His) rs150134822
NM_002878.3(RAD51D):c.878C>T (p.Ala293Val) rs769732230
NM_002878.3(RAD51D):c.883C>G (p.Leu295Val) rs752910287
NM_002878.3(RAD51D):c.899G>A (p.Arg300Gln) rs761290755
NM_002878.3(RAD51D):c.919G>A (p.Glu307Lys) rs115031549
NM_002878.3(RAD51D):c.932T>A (p.Ile311Asn) rs145309168
NM_002878.3(RAD51D):c.932T>C (p.Ile311Thr) rs145309168
NM_002878.3(RAD51D):c.950_954CAGAG[3] (p.Ala321fs) rs771998974
NM_002878.3(RAD51D):c.952G>A (p.Glu318Lys) rs876658737
NM_002878.3(RAD51D):c.955C>T (p.Gln319Ter) rs794726988
NM_002878.3(RAD51D):c.973G>A (p.Gly325Ser) rs587780106

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