ClinVar Miner

List of variants in gene RAD51D, RAD51L3-RFFL studied for breast disorder

Included ClinVar conditions (69):
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Gene type:
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Total variants: 34
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HGVS dbSNP gnomAD frequency
NM_002878.4(RAD51D):c.698A>G (p.Glu233Gly) rs28363284 0.01102
NM_002878.4(RAD51D):c.695G>A (p.Arg232Gln) rs28363283 0.00457
NM_002878.4(RAD51D):c.873C>T (p.Arg291=) rs140848654 0.00399
NM_002878.4(RAD51D):c.481-7G>A rs145832514 0.00171
NM_002878.4(RAD51D):c.568G>A (p.Ala190Thr) rs80116829 0.00167
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.26G>C (p.Cys9Ser) rs140825795 0.00037
NM_002878.4(RAD51D):c.216C>T (p.Tyr72=) rs148690585 0.00028
NM_002878.4(RAD51D):c.904-3C>T rs45478491 0.00018
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.394G>A (p.Val132Ile) rs201141245 0.00007
NM_002878.4(RAD51D):c.629C>T (p.Ala210Val) rs376855484 0.00006
NM_002878.4(RAD51D):c.957G>A (p.Gln319=) rs147669627 0.00006
NM_002878.4(RAD51D):c.796C>T (p.Arg266Cys) rs587781813 0.00004
NM_002878.4(RAD51D):c.556C>T (p.Arg186Ter) rs387906843 0.00003
NM_002878.4(RAD51D):c.164G>A (p.Arg55Gln) rs151198586 0.00002
NM_002878.4(RAD51D):c.171G>A (p.Leu57=) rs786202885 0.00002
NM_002878.4(RAD51D):c.620C>T (p.Ser207Leu) rs370228071 0.00002
NM_002878.4(RAD51D):c.898C>T (p.Arg300Ter) rs750621215 0.00002
NM_002878.4(RAD51D):c.131G>A (p.Gly44Asp) rs374730714 0.00001
NM_002878.4(RAD51D):c.27C>T (p.Cys9=) rs200487648 0.00001
NM_002878.4(RAD51D):c.491T>C (p.Leu164Pro) rs769287847 0.00001
NM_002878.4(RAD51D):c.739-10T>C rs199998187 0.00001
NM_002878.4(RAD51D):c.739-1G>A rs1555567202 0.00001
NM_002878.4(RAD51D):c.772G>A (p.Gly258Arg) rs181695922 0.00001
NM_002878.4(RAD51D):c.33C>T (p.Gly11=) rs760444811
NM_002878.4(RAD51D):c.480+1G>A rs1597862471
NM_002878.4(RAD51D):c.576+6C>G rs2142428719
NM_002878.4(RAD51D):c.738+402_*1465del
NM_002878.4(RAD51D):c.757C>T (p.Arg253Ter) rs137886232
NM_002878.4(RAD51D):c.768C>G (p.Asp256Glu) rs569428131
NM_002878.4(RAD51D):c.790_796dup (p.Arg266fs) rs2142411968

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