ClinVar Miner

List of variants in gene RAD50 reported as benign for Hereditary cancer-predisposing syndrome

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Total variants: 21
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HGVS dbSNP
NM_005732.3:c.2923-5insT
NM_005732.4(RAD50):c.1544A>G (p.Asp515Gly) rs145843634
NM_005732.4(RAD50):c.2025C>T (p.Asp675=) rs34147298
NM_005732.4(RAD50):c.2091C>T (p.Val697=) rs61747588
NM_005732.4(RAD50):c.2352T>C (p.Ser784=) rs534731345
NM_005732.4(RAD50):c.2658A>G (p.Gln886=) rs768654795
NM_005732.4(RAD50):c.2670G>A (p.Gln890=) rs112241748
NM_005732.4(RAD50):c.280A>C (p.Ile94Leu) rs28903085
NM_005732.4(RAD50):c.2910C>T (p.Asp970=) rs148269640
NM_005732.4(RAD50):c.2923-5del rs2066742
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.3253A>G (p.Ile1085Val) rs143189763
NM_005732.4(RAD50):c.379G>A (p.Val127Ile) rs28903086
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.756+7del rs377720482
NM_005732.4(RAD50):c.980G>A (p.Arg327His) rs28903091

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