ClinVar Miner

List of variants in gene combination RAD51D, RAD51L3-RFFL reported as uncertain significance by Quest Diagnostics Nichols Institute San Juan Capistrano

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Gene type:
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Total variants: 51
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HGVS dbSNP gnomAD frequency
NM_002878.4(RAD51D):c.413A>G (p.Asn138Ser) rs201676898 0.00025
NM_002878.4(RAD51D):c.434G>A (p.Arg145His) rs147264215 0.00023
NM_002878.4(RAD51D):c.*7C>T rs370985675 0.00019
NM_002878.4(RAD51D):c.137C>G (p.Ser46Cys) rs587780102 0.00010
NM_002878.4(RAD51D):c.355T>C (p.Cys119Arg) rs201313861 0.00008
NM_002878.4(RAD51D):c.973G>A (p.Gly325Ser) rs587780106 0.00008
NM_002878.4(RAD51D):c.394G>A (p.Val132Ile) rs201141245 0.00007
NM_002878.4(RAD51D):c.629C>T (p.Ala210Val) rs376855484 0.00006
NM_002878.4(RAD51D):c.715C>T (p.Arg239Trp) rs770250516 0.00006
NM_002878.4(RAD51D):c.101C>T (p.Ala34Val) rs876658968 0.00004
NM_002878.4(RAD51D):c.264-7C>T rs753529790 0.00004
NM_002878.4(RAD51D):c.493C>T (p.Arg165Trp) rs544654228 0.00004
NM_002878.4(RAD51D):c.793G>A (p.Gly265Arg) rs140285068 0.00004
NM_002878.4(RAD51D):c.796C>T (p.Arg266Cys) rs587781813 0.00004
NM_002878.4(RAD51D):c.797G>A (p.Arg266His) rs779808083 0.00004
NM_002878.4(RAD51D):c.53A>G (p.Gln18Arg) rs546225564 0.00003
NM_002878.4(RAD51D):c.5G>C (p.Gly2Ala) rs763716638 0.00003
NM_002878.4(RAD51D):c.878C>T (p.Ala293Val) rs769732230 0.00003
NM_002878.4(RAD51D):c.911G>A (p.Gly304Asp) rs200615280 0.00003
NM_002878.4(RAD51D):c.171G>A (p.Leu57=) rs786202885 0.00002
NM_002878.4(RAD51D):c.868C>T (p.Arg290Trp) rs527964137 0.00002
NM_002878.4(RAD51D):c.872G>A (p.Arg291His) rs150134822 0.00002
NM_002878.4(RAD51D):c.131G>A (p.Gly44Asp) rs374730714 0.00001
NM_002878.4(RAD51D):c.345+5A>G rs878854562 0.00001
NM_002878.4(RAD51D):c.356G>A (p.Cys119Tyr) rs759730492 0.00001
NM_002878.4(RAD51D):c.374C>T (p.Ala125Val) rs1390812423 0.00001
NM_002878.4(RAD51D):c.431C>T (p.Ser144Phe) rs587781875 0.00001
NM_002878.4(RAD51D):c.433C>T (p.Arg145Cys) rs755173206 0.00001
NM_002878.4(RAD51D):c.481-5T>G rs374382703 0.00001
NM_002878.4(RAD51D):c.49A>G (p.Ile17Val) rs1002032036 0.00001
NM_002878.4(RAD51D):c.550G>A (p.Glu184Lys) rs200009601 0.00001
NM_002878.4(RAD51D):c.607G>A (p.Val203Met) rs730881947 0.00001
NM_002878.4(RAD51D):c.187G>A (p.Ala63Thr) rs777402267
NM_002878.4(RAD51D):c.194C>G (p.Pro65Arg)
NM_002878.4(RAD51D):c.208G>T (p.Asp70Tyr)
NM_002878.4(RAD51D):c.295A>C (p.Thr99Pro) rs746416079
NM_002878.4(RAD51D):c.331A>C (p.Ser111Arg) rs2091620231
NM_002878.4(RAD51D):c.335G>A (p.Gly112Asp) rs587782848
NM_002878.4(RAD51D):c.346-8A>C rs756059587
NM_002878.4(RAD51D):c.402T>C (p.Tyr134=) rs1419080369
NM_002878.4(RAD51D):c.412A>C (p.Asn138His) rs141690729
NM_002878.4(RAD51D):c.412A>G (p.Asn138Asp) rs141690729
NM_002878.4(RAD51D):c.441C>A (p.Leu147=) rs1567728273
NM_002878.4(RAD51D):c.471G>C (p.Glu157Asp) rs55942401
NM_002878.4(RAD51D):c.515C>T (p.Ala172Val) rs1413648665
NM_002878.4(RAD51D):c.573G>A (p.Gln191=) rs1597861626
NM_002878.4(RAD51D):c.629C>A (p.Ala210Glu) rs376855484
NM_002878.4(RAD51D):c.668-3C>T
NM_002878.4(RAD51D):c.66C>G (p.Ser22Arg) rs876660902
NM_002878.4(RAD51D):c.802T>A (p.Trp268Arg) rs755965977
NM_002878.4(RAD51D):c.804G>T (p.Trp268Cys) rs1597856016

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