ClinVar Miner

List of variants in gene RAD50 studied for not specified

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Gene type:
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Total variants: 53
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HGVS dbSNP
NM_005732.4(RAD50):c.-38= rs4526098
NM_005732.4(RAD50):c.1052-6del
NM_005732.4(RAD50):c.1094G>A (p.Arg365Gln) rs146370443
NM_005732.4(RAD50):c.1277A>G (p.Gln426Arg) rs145428112
NM_005732.4(RAD50):c.1287A>G (p.Ile429Met) rs1554098314
NM_005732.4(RAD50):c.129+5G>A rs587781409
NM_005732.4(RAD50):c.1336A>G (p.Lys446Glu) rs149217423
NM_005732.4(RAD50):c.1353T>A (p.Ser451Arg) rs587782523
NM_005732.4(RAD50):c.1534G>T (p.Ala512Ser) rs147366706
NM_005732.4(RAD50):c.1605T>C (p.Arg535=) rs878854785
NM_005732.4(RAD50):c.1663A>G (p.Ile555Val) rs201120953
NM_005732.4(RAD50):c.1677C>G (p.His559Gln) rs142619269
NM_005732.4(RAD50):c.1677C>T (p.His559=) rs142619269
NM_005732.4(RAD50):c.1689A>G (p.Leu563=) rs1580994836
NM_005732.4(RAD50):c.1911T>A (p.Asp637Glu) rs144749616
NM_005732.4(RAD50):c.1970-7A>C rs370034340
NM_005732.4(RAD50):c.2091C>T (p.Val697=) rs61747588
NM_005732.4(RAD50):c.2173C>T (p.Arg725Trp) rs369560280
NM_005732.4(RAD50):c.2209C>G (p.Gln737Glu) rs549559726
NM_005732.4(RAD50):c.2468G>A (p.Arg823Gln) rs572533256
NM_005732.4(RAD50):c.2472T>G (p.Thr824=) rs1358470664
NM_005732.4(RAD50):c.2525T>C (p.Val842Ala) rs28903093
NM_005732.4(RAD50):c.259C>T (p.Arg87Cys) rs143802516
NM_005732.4(RAD50):c.260G>A (p.Arg87His) rs374561375
NM_005732.4(RAD50):c.2670G>A (p.Gln890=) rs112241748
NM_005732.4(RAD50):c.2688T>C (p.Thr896=) rs537257801
NM_005732.4(RAD50):c.2693T>G (p.Val898Gly)
NM_005732.4(RAD50):c.2718+10T>G rs765764447
NM_005732.4(RAD50):c.2750C>T (p.Thr917Ile) rs562172843
NM_005732.4(RAD50):c.280A>C (p.Ile94Leu) rs28903085
NM_005732.4(RAD50):c.281T>C (p.Ile94Thr) rs768127412
NM_005732.4(RAD50):c.2840T>C (p.Ile947Thr) rs150401251
NM_005732.4(RAD50):c.2910C>T (p.Asp970=) rs148269640
NM_005732.4(RAD50):c.3036+5G>A rs181016343
NM_005732.4(RAD50):c.3037-3T>C rs115737081
NM_005732.4(RAD50):c.3153G>A (p.Leu1051=) rs35800931
NM_005732.4(RAD50):c.3165-4A>T rs104895050
NM_005732.4(RAD50):c.3165-8T>G rs369581851
NM_005732.4(RAD50):c.3206G>T (p.Arg1069Ile) rs769003601
NM_005732.4(RAD50):c.3230G>A (p.Arg1077Gln) rs104895051
NM_005732.4(RAD50):c.323A>G (p.Lys108Arg) rs542347773
NM_005732.4(RAD50):c.3253A>G (p.Ile1085Val) rs143189763
NM_005732.4(RAD50):c.353T>C (p.Ile118Thr) rs200472836
NM_005732.4(RAD50):c.551+19G>A rs17166050
NM_005732.4(RAD50):c.572C>T (p.Thr191Ile) rs2230017
NM_005732.4(RAD50):c.671G>A (p.Arg224His) rs28903088
NM_005732.4(RAD50):c.677A>C (p.Gln226Pro) rs1060501953
NM_005732.4(RAD50):c.756+7del rs377720482
NM_005732.4(RAD50):c.785T>G (p.Leu262Arg) rs201728859
NM_005732.4(RAD50):c.885+11G>A rs117081789
NM_005732.4(RAD50):c.927C>T (p.His309=) rs758239327
NM_005732.4(RAD50):c.943G>T (p.Val315Leu) rs28903090
NM_005732.4(RAD50):c.980G>A (p.Arg327His) rs28903091

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