ClinVar Miner

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

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Gene type:
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Total variants: 50
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HGVS dbSNP gnomAD frequency
NM_005732.4(RAD50):c.551+19G>A rs17166050 0.17902
NM_005732.4(RAD50):c.2025C>T (p.Asp675=) rs34147298 0.02660
NM_005732.4(RAD50):c.3037-3T>C rs115737081 0.00627
NM_005732.4(RAD50):c.572C>T (p.Thr191Ile) rs2230017 0.00469
NM_005732.4(RAD50):c.2910C>T (p.Asp970=) rs148269640 0.00422
NM_005732.4(RAD50):c.3153G>A (p.Leu1051=) rs35800931 0.00325
NM_005732.4(RAD50):c.280A>C (p.Ile94Leu) rs28903085 0.00300
NM_005732.4(RAD50):c.2670G>A (p.Gln890=) rs112241748 0.00216
NM_005732.4(RAD50):c.980G>A (p.Arg327His) rs28903091 0.00207
NM_005732.4(RAD50):c.3165-8T>G rs369581851 0.00189
NM_005732.4(RAD50):c.2091C>T (p.Val697=) rs61747588 0.00156
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.3165-4A>T rs104895050 0.00133
NM_005732.4(RAD50):c.3253A>G (p.Ile1085Val) rs143189763 0.00111
NM_005732.4(RAD50):c.3036+5G>A rs181016343 0.00078
NM_005732.4(RAD50):c.1544A>G (p.Asp515Gly) rs145843634 0.00076
NM_005732.4(RAD50):c.885+11G>A rs117081789 0.00071
NM_005732.4(RAD50):c.671G>A (p.Arg224His) rs28903088 0.00065
NM_005732.4(RAD50):c.2397G>C (p.Gln799His) rs61749630 0.00036
NM_005732.4(RAD50):c.2647C>T (p.Arg883Cys) rs138749920 0.00032
NM_005732.4(RAD50):c.2718+13A>G rs372194471 0.00019
NM_005732.4(RAD50):c.2658A>G (p.Gln886=) rs768654795 0.00006
NM_005732.4(RAD50):c.1720A>C (p.Lys574Gln) rs779597467 0.00002
NM_005732.4(RAD50):c.1628A>G (p.Lys543Arg) rs766041105 0.00001
NM_005732.4(RAD50):c.2651G>A (p.Arg884His) rs558302979 0.00001
NM_005732.3:c.2923-5insT
NM_005732.4(RAD50):c.1052-6del rs201800554
NM_005732.4(RAD50):c.1052-6dup rs201800554
NM_005732.4(RAD50):c.130-13dup
NM_005732.4(RAD50):c.1636-10_1636-9dup rs762814289
NM_005732.4(RAD50):c.1636-9del rs762814289
NM_005732.4(RAD50):c.1636-9dup rs762814289
NM_005732.4(RAD50):c.1794-3dup rs1554098578
NM_005732.4(RAD50):c.1875C>T (p.Tyr625=) rs149201802
NM_005732.4(RAD50):c.1970-4del
NM_005732.4(RAD50):c.1970-4dup
NM_005732.4(RAD50):c.2121T>C (p.Leu707=) rs377625784
NM_005732.4(RAD50):c.2352T>C (p.Ser784=) rs534731345
NM_005732.4(RAD50):c.2718+25del rs532725532
NM_005732.4(RAD50):c.2718+25dup
NM_005732.4(RAD50):c.2719-11del rs1210923518
NM_005732.4(RAD50):c.2719-3del rs1751026470
NM_005732.4(RAD50):c.2719-3dup rs1751026470
NM_005732.4(RAD50):c.2923-5del rs2066742
NM_005732.4(RAD50):c.2923-5dup rs2066742
NM_005732.4(RAD50):c.3164+14del rs148895884
NM_005732.4(RAD50):c.3165-5del rs1751207168
NM_005732.4(RAD50):c.3389+18del
NM_005732.4(RAD50):c.756+7del rs377720482

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