ClinVar Miner

List of variants in gene RAD50 reported as likely benign for not provided

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Gene type:
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Total variants: 48
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HGVS dbSNP gnomAD frequency
NM_005732.4(RAD50):c.2207+296G>A rs115976537 0.01975
NM_005732.4(RAD50):c.1970-65G>A rs148383531 0.01409
NM_005732.4(RAD50):c.130-265A>G rs115198557 0.00903
NM_005732.4(RAD50):c.572C>T (p.Thr191Ile) rs2230017 0.00469
NM_005732.4(RAD50):c.1794-193A>C rs73259670 0.00440
NM_005732.4(RAD50):c.757-63C>T rs74861356 0.00436
NM_005732.4(RAD50):c.3164+49G>C rs143829407 0.00361
NM_005732.4(RAD50):c.3036+151C>T rs546261138 0.00308
NM_005732.4(RAD50):c.280A>C (p.Ile94Leu) rs28903085 0.00300
NM_005732.4(RAD50):c.980G>A (p.Arg327His) rs28903091 0.00207
NM_005732.4(RAD50):c.379G>A (p.Val127Ile) rs28903086 0.00146
NM_005732.4(RAD50):c.943G>T (p.Val315Leu) rs28903090 0.00141
NM_005732.4(RAD50):c.3253A>G (p.Ile1085Val) rs143189763 0.00111
NM_005732.4(RAD50):c.1534G>T (p.Ala512Ser) rs147366706 0.00079
NM_005732.4(RAD50):c.3036+5G>A rs181016343 0.00078
NM_005732.4(RAD50):c.3122A>G (p.His1041Arg) rs149577978 0.00064
NM_005732.4(RAD50):c.260G>A (p.Arg87His) rs374561375 0.00042
NM_005732.4(RAD50):c.2647C>T (p.Arg883Cys) rs138749920 0.00032
NM_005732.4(RAD50):c.1094G>A (p.Arg365Gln) rs146370443 0.00026
NM_005732.4(RAD50):c.2288G>A (p.Arg763His) rs141989813 0.00026
NM_005732.4(RAD50):c.1677C>T (p.His559=) rs142619269 0.00022
NM_005732.4(RAD50):c.1554G>C (p.Leu518=) rs148214481 0.00013
NM_005732.4(RAD50):c.204C>T (p.His68=) rs28903084 0.00010
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.1602A>G (p.Thr534=) rs150348197 0.00004
NM_005732.4(RAD50):c.1686A>G (p.Glu562=) rs751250564 0.00003
NM_005732.4(RAD50):c.2619G>A (p.Glu873=) rs751662539 0.00003
NM_005732.4(RAD50):c.39G>A (p.Arg13=) rs779005784 0.00003
NM_005732.4(RAD50):c.1497C>G (p.Thr499=) rs1023524138 0.00002
NM_005732.4(RAD50):c.1540T>C (p.Leu514=) rs199702045 0.00002
NM_005732.4(RAD50):c.2113C>T (p.Leu705=) rs779776271 0.00002
NM_005732.4(RAD50):c.2013T>C (p.Thr671=) rs1345954274 0.00001
NM_005732.4(RAD50):c.2651G>A (p.Arg884His) rs558302979 0.00001
NM_005732.4(RAD50):c.3288A>G (p.Gln1096=) rs878854798 0.00001
NM_005732.4(RAD50):c.1005A>G (p.Glu335=) rs747098394
NM_005732.4(RAD50):c.129+184T>G rs2548986
NM_005732.4(RAD50):c.1969+232G>A rs143331722
NM_005732.4(RAD50):c.213+203T>C
NM_005732.4(RAD50):c.2207+203dup rs34713748
NM_005732.4(RAD50):c.2524+236del rs879833449
NM_005732.4(RAD50):c.2589A>G (p.Leu863=) rs1260371384
NM_005732.4(RAD50):c.288G>C (p.Val96=) rs876658184
NM_005732.4(RAD50):c.3027T>C (p.Asp1009=) rs773757483
NM_005732.4(RAD50):c.3177G>A (p.Lys1059=) rs786202762
NM_005732.4(RAD50):c.365+7G>A rs1554097580
NM_005732.4(RAD50):c.579G>A (p.Arg193=) rs1554097802
NM_005732.4(RAD50):c.756+7del rs377720482

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