ClinVar Miner

List of variants in gene RAD50 studied for cancer

Included ClinVar conditions (475):
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Gene type:
ClinVar version:
Total variants: 37
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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.214-44G>A rs74769721 0.02590
NM_005732.4(RAD50):c.1052-38C>T rs104895045 0.01852
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.2091C>T (p.Val697=) rs61747588 0.00156
NM_005732.4(RAD50):c.3165-4A>T rs104895050 0.00133
NM_005732.4(RAD50):c.885+11G>A rs117081789 0.00071
NM_005732.4(RAD50):c.1094G>A (p.Arg365Gln) rs146370443 0.00026
NM_005732.4(RAD50):c.760C>T (p.Arg254Cys) rs555367432 0.00009
NM_005732.4(RAD50):c.1932G>A (p.Arg644=) rs375978877 0.00004
NM_005732.4(RAD50):c.2047G>A (p.Val683Ile) rs367925756 0.00004
NM_005732.4(RAD50):c.2014C>T (p.Gln672Ter) rs142947311 0.00002
NM_005732.4(RAD50):c.1513A>G (p.Ile505Val) rs193921012 0.00001
NM_005732.4(RAD50):c.2530A>C (p.Ser844Arg) rs373817937 0.00001
NM_005732.4(RAD50):c.323A>G (p.Lys108Arg) rs542347773 0.00001
NM_005732.4(RAD50):c.102G>A (p.Leu34=) rs876659395
NM_005732.4(RAD50):c.1090A>G (p.Ile364Val) rs1750641668
NM_005732.4(RAD50):c.136A>G (p.Ile46Val)
NM_005732.4(RAD50):c.1829A>G (p.His610Arg) rs527518431
NM_005732.4(RAD50):c.1875C>G (p.Tyr625Ter) rs149201802
NM_005732.4(RAD50):c.1928A>T (p.Asp643Val) rs1750764737
NM_005732.4(RAD50):c.2046del (p.Val683fs)
NM_005732.4(RAD50):c.2221G>C (p.Asp741His)
NM_005732.4(RAD50):c.2524+1_2524+9del
NM_005732.4(RAD50):c.3195C>T (p.Asp1065=) rs786201980
NM_005732.4(RAD50):c.326_329del (p.Thr109fs) rs587780155
NM_005732.4(RAD50):c.398G>T (p.Cys133Phe) rs786201788
NM_005732.4(RAD50):c.452_453dup (p.Asn152Ter) rs1561635887
NM_005732.4(RAD50):c.587G>A (p.Arg196His) rs764784659
NM_005732.4(RAD50):c.656A>G (p.Lys219Arg)
NM_005732.4(RAD50):c.670C>T (p.Arg224Cys) rs753136372

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