Oncogene database

COSMIC confirmed somatic mutation   [Top]

c.162G>A; p.S54S; 12:51118733-51118733

c.769C>T; p.R257*; 12:51107295-51107295

c.243C>G; p.L81L; 12:51118652-51118652

c.1152G>A; p.R384R; 12:51099779-51099779

c.794A>T; p.Y265F; 12:51107270-51107270

c.943G>C; p.E315Q; 12:51104178-51104178

c.787G>A; p.E263K; 12:51107277-51107277

c.464C>T; p.P155L; 12:51110977-51110977

c.1015C>T; p.R339*; 12:51103715-51103715

c.610G>A; p.E204K; 12:51109228-51109228

c.746C>T; p.T249M; 12:51107318-51107318

c.844G>A; p.E282K; 12:51106598-51106598

c.1016G>A; p.R339Q; 12:51103714-51103714

c.1016G>A; p.R339Q; 12:51103714-51103714

c.261G>A; p.T87T; 12:51118634-51118634

c.1445C>T; p.A482V; 12:51096015-51096015

c.918-1G>T; p.?; 12:51104204-51104204

c.771A>G; p.R257R; 12:51107293-51107293

c.1238A>G; p.Q413R; 12:51099693-51099693

c.1275C>T; p.F425F; 12:51099656-51099656

c.1272C>A; p.F424L; 12:51099659-51099659

c.113A>G; p.Y38C; 12:51172310-51172310

c.706A>G; p.K236E; 12:51109132-51109132

c.1267A>G; p.T423A; 12:51099664-51099664

c.1063G>A; p.A355T; 12:51102023-51102023

c.1277T>C; p.V426A; 12:51098918-51098918

c.1120G>A; p.G374R; 12:51101966-51101966

c.34G>A; p.E12K; 12:51172389-51172389

c.1201T>A; p.L401M; 12:51099730-51099730

c.718-1G>A; p.?; 12:51107347-51107347

c.663C>T; p.N221N; 12:51109175-51109175

c.203A>G; p.Q68R; 12:51118692-51118692

c.204A>G; p.Q68Q; 12:51118691-51118691

c.581_582delCA; p.T194fs*26; 12:51109256-51109257

c.581_582delCA; p.T194fs*26; 12:51109256-51109257

c.1016G>A; p.R339Q; 12:51103714-51103714

c.361C>T; p.R121C; 12:51116411-51116411

c.1016G>A; p.R339Q; 12:51103714-51103714

c.1016G>A; p.R339Q; 12:51103714-51103714

c.691G>A; p.A231T; 12:51109147-51109147

c.918-1G>T; p.?; 12:51104204-51104204

c.52T>C; p.L18L; 12:51172371-51172371

c.1121_1127delGAATCAG; p.G374fs*6; 12:51101959-51101965

c.627C>A; p.F209L; 12:51109211-51109211

c.293G>A; p.R98Q; 12:51117729-51117729

c.569A>G; p.H190R; 12:51109269-51109269

c.1109G>C; p.G370A; 12:51101977-51101977

c.1331T>C; p.I444T; 12:51098864-51098864

c.1331T>C; p.I444T; 12:51098864-51098864

c.760delA; p.M254fs*105; 12:51107304-51107304

c.292C>T; p.R98*; 12:51117730-51117730

c.1338G>A; p.Q446Q; 12:51098857-51098857

c.730G>A; p.D244N; 12:51107334-51107334

c.730G>A; p.D244N; 12:51107334-51107334

c.1115C>A; p.A372E; 12:51101971-51101971

c.955C>G; p.P319A; 12:51104166-51104166

c.1127G>C; p.R376T; 12:51101959-51101959

c.1368C>A; p.S456R; 12:51098827-51098827

c.423G>A; p.R141R; 12:51116349-51116349

c.164G>A; p.S55N; 12:51118731-51118731

c.795T>C; p.Y265Y; 12:51107269-51107269

c.1098C>G; p.I366M; 12:51101988-51101988

c.854A>T; p.Y285F; 12:51106588-51106588

c.1085G>C; p.R362T; 12:51102001-51102001

c.465G>T; p.P155P; 12:51110976-51110976

c.1016G>A; p.R339Q; 12:51103714-51103714

c.261G>A; p.T87T; 12:51118634-51118634

c.204A>T; p.Q68H; 12:51118691-51118691

c.1352C>T; p.S451F; 12:51098843-51098843

c.120G>A; p.M40I; 12:51172303-51172303

c.420G>A; p.W140*; 12:51116352-51116352

c.197C>T; p.P66L; 12:51118698-51118698

c.535C>T; p.P179S; 12:51110906-51110906

c.627C>T; p.F209F; 12:51109211-51109211

c.267C>T; p.L89L; 12:51118628-51118628

c.464C>G; p.P155R; 12:51110977-51110977

c.1162C>T; p.P388S; 12:51099769-51099769

c.328G>A; p.E110K; 12:51117694-51117694

c.1354C>T; p.P452S; 12:51098841-51098841

c.890C>T; p.S297F; 12:51106552-51106552

c.1357T>C; p.C453R; 12:51098838-51098838

c.292C>T; p.R98*; 12:51117730-51117730

c.192C>T; p.I64I; 12:51118703-51118703

c.960C>T; p.V320V; 12:51104161-51104161

c.1397T>A; p.I466N; 12:51098798-51098798

c.1272C>T; p.F424F; 12:51099659-51099659

c.689C>T; p.S230L; 12:51109149-51109149

c.1308A>G; p.T436T; 12:51098887-51098887

c.1014T>C; p.H338H; 12:51103716-51103716

c.10G>A; p.A4T; 12:51172413-51172413

c.1322C>T; p.T441I; 12:51098873-51098873

c.1205G>T; p.R402M; 12:51099726-51099726

c.717+2T>C; p.?; 12:51109119-51109119

c.858C>T; p.V286V; 12:51106584-51106584

c.157G>A; p.E53K; 12:51118738-51118738