ClinVar Miner

List of variants in gene RAD50 reported as uncertain significance for not provided

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Gene type:
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Total variants: 31
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HGVS dbSNP
NM_005732.4(RAD50):c.1094G>A (p.Arg365Gln) rs146370443
NM_005732.4(RAD50):c.1117T>G (p.Ser373Ala) rs587780146
NM_005732.4(RAD50):c.1211A>G (p.Gln404Arg) rs200017020
NM_005732.4(RAD50):c.1277A>G (p.Gln426Arg) rs145428112
NM_005732.4(RAD50):c.1328T>C (p.Ile443Thr) rs587780148
NM_005732.4(RAD50):c.137T>A (p.Ile46Asn) rs587780149
NM_005732.4(RAD50):c.1534G>T (p.Ala512Ser) rs147366706
NM_005732.4(RAD50):c.1838A>G (p.Asn613Ser) rs587780151
NM_005732.4(RAD50):c.1911T>A (p.Asp637Glu) rs144749616
NM_005732.4(RAD50):c.2177G>A (p.Arg726His) rs28903092
NM_005732.4(RAD50):c.2213G>A (p.Ser738Asn) rs587780152
NM_005732.4(RAD50):c.2288G>A (p.Arg763His) rs141989813
NM_005732.4(RAD50):c.2397G>C (p.Gln799His) rs61749630
NM_005732.4(RAD50):c.2525T>C (p.Val842Ala) rs28903093
NM_005732.4(RAD50):c.2548C>T (p.Arg850Cys) rs181961360
NM_005732.4(RAD50):c.2563G>T (p.Asp855Tyr) rs144911328
NM_005732.4(RAD50):c.260G>A (p.Arg87His) rs374561375
NM_005732.4(RAD50):c.2647C>T (p.Arg883Cys) rs138749920
NM_005732.4(RAD50):c.2651G>A (p.Arg884His) rs558302979
NM_005732.4(RAD50):c.265G>A (p.Val89Ile) rs151109830
NM_005732.4(RAD50):c.2750C>T (p.Thr917Ile) rs562172843
NM_005732.4(RAD50):c.2840T>C (p.Ile947Thr) rs150401251
NM_005732.4(RAD50):c.3036+5G>A rs181016343
NM_005732.4(RAD50):c.3253A>G (p.Ile1085Val) rs143189763
NM_005732.4(RAD50):c.3310T>C (p.Tyr1104His) rs147545169
NM_005732.4(RAD50):c.379G>A (p.Val127Ile) rs28903086
NM_005732.4(RAD50):c.625G>C (p.Glu209Gln) rs587780158
NM_005732.4(RAD50):c.671G>A (p.Arg224His) rs28903088
NM_005732.4(RAD50):c.673G>A (p.Asp225Asn) rs587780159
NM_005732.4(RAD50):c.943G>T (p.Val315Leu) rs28903090
NM_005732.4(RAD50):c.980G>A (p.Arg327His) rs28903091

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