ClinVar Miner

List of variants in gene RAD50 reported as uncertain significance by GeneKor MSA

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Gene type:
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Total variants: 17
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HGVS dbSNP
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.1429C>A (p.Leu477Met) rs1211437074
NM_005732.4(RAD50):c.1604G>A (p.Arg535His) rs200548021
NM_005732.4(RAD50):c.1663A>G (p.Ile555Val) rs201120953
NM_005732.4(RAD50):c.1680T>G (p.Ser560Arg) rs786203901
NM_005732.4(RAD50):c.2177G>A (p.Arg726His) rs28903092
NM_005732.4(RAD50):c.2288G>A (p.Arg763His) rs141989813
NM_005732.4(RAD50):c.2492A>G (p.Glu831Gly) rs772155267
NM_005732.4(RAD50):c.2604T>G (p.Asn868Lys) rs786202498
NM_005732.4(RAD50):c.281T>C (p.Ile94Thr) rs768127412
NM_005732.4(RAD50):c.3036+5G>A rs181016343
NM_005732.4(RAD50):c.34G>C (p.Val12Leu) rs755022536
NM_005732.4(RAD50):c.578G>A (p.Arg193Gln) rs776046799
NM_005732.4(RAD50):c.587G>A (p.Arg196His) rs764784659
NM_005732.4(RAD50):c.695C>A (p.Ala232Asp) rs28903089
NM_005732.4(RAD50):c.785T>G (p.Leu262Arg) rs201728859

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