ClinVar Miner

List of variants in gene RAD50 reported by PreventionGenetics, part of Exact Sciences

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Gene type:
ClinVar version:
Total variants: 46
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HGVS dbSNP gnomAD frequency
NM_005732.4(RAD50):c.551+19G>A rs17166050 0.17902
NM_005732.4(RAD50):c.2670G>A (p.Gln890=) rs112241748 0.00216
NM_005732.4(RAD50):c.980G>A (p.Arg327His) rs28903091 0.00207
NM_005732.4(RAD50):c.1534G>T (p.Ala512Ser) rs147366706 0.00079
NM_005732.4(RAD50):c.671G>A (p.Arg224His) rs28903088 0.00065
NM_005732.4(RAD50):c.3122A>G (p.His1041Arg) rs149577978 0.00064
NM_005732.4(RAD50):c.921A>G (p.Leu307=) rs144639596 0.00062
NM_005732.4(RAD50):c.1094G>A (p.Arg365Gln) rs146370443 0.00026
NM_005732.4(RAD50):c.2177G>A (p.Arg726His) rs28903092 0.00025
NM_005732.4(RAD50):c.1677C>T (p.His559=) rs142619269 0.00022
NM_005732.4(RAD50):c.259C>T (p.Arg87Cys) rs143802516 0.00014
NM_005732.4(RAD50):c.1554G>C (p.Leu518=) rs148214481 0.00013
NM_005732.4(RAD50):c.2548C>T (p.Arg850Cys) rs181961360 0.00010
NM_005732.4(RAD50):c.1211A>G (p.Gln404Arg) rs200017020 0.00009
NM_005732.4(RAD50):c.1026A>G (p.Glu342=) rs140079790 0.00006
NM_005732.4(RAD50):c.2046C>T (p.Pro682=) rs759476003 0.00004
NM_005732.4(RAD50):c.1868C>T (p.Ser623Phe) rs760464509 0.00003
NM_005732.4(RAD50):c.1540T>C (p.Leu514=) rs199702045 0.00002
NM_005732.4(RAD50):c.2298C>T (p.Asn766=) rs144186349 0.00002
NM_005732.4(RAD50):c.1129C>G (p.Gln377Glu) rs773142865 0.00001
NM_005732.4(RAD50):c.129+5G>A rs587781409 0.00001
NM_005732.4(RAD50):c.1698G>A (p.Leu566=) rs749631904 0.00001
NM_005732.4(RAD50):c.1958C>A (p.Ser653Ter) rs587781904 0.00001
NM_005732.4(RAD50):c.2108C>A (p.Ser703Tyr) rs769143998 0.00001
NM_005732.4(RAD50):c.2790C>A (p.Ile930=) rs786202014 0.00001
NM_005732.4(RAD50):c.3384T>A (p.Leu1128=) rs1060504387 0.00001
NM_005732.4(RAD50):c.915T>C (p.Asn305=) rs759379314 0.00001
NM_005732.4(RAD50):c.94dup (p.Thr32fs) rs587781625 0.00001
NM_005732.4(RAD50):c.1381A>T (p.Lys461Ter) rs1580993516
NM_005732.4(RAD50):c.1435C>T (p.Gln479Ter)
NM_005732.4(RAD50):c.1455A>T (p.Glu485Asp) rs1750690947
NM_005732.4(RAD50):c.2202del (p.Pro734_Met735insTer) rs786201789
NM_005732.4(RAD50):c.2352T>C (p.Ser784=) rs534731345
NM_005732.4(RAD50):c.2525-6G>A rs745693687
NM_005732.4(RAD50):c.2538T>G (p.Ile846Met) rs1220188545
NM_005732.4(RAD50):c.2559A>G (p.Ile853Met) rs2149847715
NM_005732.4(RAD50):c.2589A>G (p.Leu863=) rs1260371384
NM_005732.4(RAD50):c.2724T>C (p.Ala908=) rs780078592
NM_005732.4(RAD50):c.3000T>C (p.Asp1000=) rs1554099393
NM_005732.4(RAD50):c.3036+2dup
NM_005732.4(RAD50):c.3164+9T>C rs1159952143
NM_005732.4(RAD50):c.3389+1G>A rs762648843
NM_005732.4(RAD50):c.386T>C (p.Leu129Pro)
NM_005732.4(RAD50):c.670C>T (p.Arg224Cys) rs753136372
NM_005732.4(RAD50):c.885+10G>C rs1438201235
NM_005732.4(RAD50):c.999_1002del (p.Asn333fs) rs1580992265

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