PCGP germline mutation   [Top]

PCGP somatic mutation   [Top]

COSMIC somatic mutation   [Top]

c.2992-10delt; p.?;

c.5206C>A; p.L1736I;

c.3146A>G; p.D1049G;

c.4663C>T; p.H1555Y;

c.4280G>A; p.R1427Q;

c.4959-7delt; p.?;

c.2748G>A; p.P916P;

c.2349C>G; p.V783V;

c.920G>A; p.W307*;

c.2727C>G; p.L909L;

c.2352_2364del13; p.D785fs*17;

c.4020G>A; p.S1340S;

c.285C>G; p.A95A;

c.1639+10C>T; p.?;

c.5163C>A; p.T1721T;

c.3410A>G; p.Y1137C;

c.3507G>A; p.P1169P;

c.253G>A; p.A85T;

c.3292C>T; p.H1098Y;

c.3551-2A>C; p.?;

c.1297G>A; p.E433K;

c.1298A>C; p.E433A;

c.2747C>G; p.P916R;

c.5266A>G; p.I1756V;

c.3608A>C; p.K1203T;

c.125A>T; p.N42I;

c.338A>C; p.E113A;

c.953G>C; p.R318P;

c.1910A>T; p.Q637L;

c.1398G>A; p.M466I;

c.4666G>A; p.G1556S;

c.1713G>A; p.Q571Q;

c.3050T>C; p.I1017T;

c.2902G>A; p.A968T;

c.499C>T; p.R167C;

c.416C>G; p.S139C;

c.3697C>T; p.P1233S;

c.2881C>T; p.R961C;

c.3814C>T; p.R1272C;

c.5269C>T; p.R1757W;

c.1652T>G; p.L551*;

c.2733_2741delTGACGGGCA; p.G913_D915delGHD;

c.4020G>A; p.S1340S;

c.1475A>G; p.N492S;

c.93A>G; p.Q31Q;

c.2710G>T; p.E904*;

c.719A>T; p.K240M;

c.5298C>G; p.S1766R;

c.2866G>A; p.V956M;

c.3726G>A; p.Q1242Q;

c.2558G>T; p.C853F; 1:10308776-10308776

c.4374+2T>C; p.?; 1:10347892-10347892

c.2322C>T; p.F774F;

c.984G>T; p.A328A;

c.622A>G; p.T208A;

c.4561G>A; p.D1521N;

c.4236G>A; p.Q1412Q;

c.2024G>A; p.R675Q;

c.1259C>G; p.S420C;

c.5042G>T; p.R1681L;

c.2616C>T; p.S872S;

c.3908A>G; p.N1303S;

c.4942G>C; p.E1648Q;

c.4714G>T; p.D1572Y;

c.1579G>T; p.G527W;

c.2680G>A; p.V894M;

c.701C>A; p.T234N;

c.4123C>G; p.L1375V;

c.4167G>T; p.S1389S;

c.3542C>A; p.S1181Y;

c.4464C>T; p.L1488L;

c.2079G>T; p.W693C;

c.970G>T; p.A324S;

c.1888C>G; p.Q630E;

c.3514C>T; p.R1172*;

c.4233G>A; p.M1411I;

c.4784C>G; p.S1595C;

c.4525G>A; p.E1509K;

c.2316G>T; p.R772S;

c.88A>G; p.M30V;

c.4113A>T; p.P1371P;

c.458G>C; p.R153T;

c.552G>A; p.L184L;

c.1569A>T; p.I523I;

c.1640-2A>T; p.?;

c.1640-2A>T; p.?;

c.5269C>T; p.R1757W;

c.3820C>T; p.R1274W;

c.1711C>G; p.Q571E;

c.4219G>T; p.G1407C;

c.3774C>T; p.S1258S;

c.1239T>C; p.S413S;

c.4671C>T; p.S1557S;

c.2854G>C; p.E952Q;

c.5136G>A; p.Q1712Q;

c.2689G>A; p.A897T;

c.4189G>A; p.E1397K;

c.4176C>A; p.V1392V;

c.3189C>T; p.N1063N;

c.5295G>A; p.P1765P;

c.3830C>A; p.P1277H;

c.226G>T; p.D76Y;

c.2623A>G; p.T875A;

c.2494G>A; p.D832N;

c.3623T>C; p.V1208A;

c.1880A>G; p.D627G;

c.4984C>A; p.L1662I;

c.3774C>T; p.S1258S;

c.4945G>T; p.E1649*;

c.2024G>A; p.R675Q;

c.5152-2A>C; p.?;

c.123G>T; p.K41N;

c.2558G>T; p.C853F; 1:10308776-10308776

c.306A>G; p.G102G;

c.1730G>A; p.R577H;

c.504G>A; p.V168V;

c.2327G>A; p.R776H;

c.186C>T; p.P62P;

c.4055C>T; p.A1352V;

c.2344G>A; p.E782K;

c.3841G>A; p.E1281K;

c.4957A>C; p.S1653R;

c.3396A>C; p.E1132D;

c.4531G>A; p.A1511T;

c.5304G>A; p.S1768S;

c.4275T>A; p.Y1425*;

c.3399A>G; p.S1133S;

c.1838G>T; p.W613L;

c.3599G>A; p.S1200N;

c.4313G>T; p.R1438L;

c.3934G>C; p.E1312Q;

c.3995G>T; p.G1332V;

c.2060A>C; p.E687A;

c.3107G>A; p.R1036Q;

c.4448C>T; p.S1483L;

c.1296G>A; p.K432K;

c.1899G>T; p.E633D;

c.96C>T; p.G32G;

c.227A>G; p.D76G;

c.4759T>C; p.S1587P;

c.1086G>T; p.L362L;

c.4672G>A; p.V1558I;

c.1855G>A; p.E619K;

c.1830T>C; p.P610P;

c.2848G>A; p.V950I;

c.997G>A; p.D333N;

c.227A>G; p.D76G;

c.1034C>T; p.A345V;

c.4387C>A; p.R1463S;

c.4166C>T; p.S1389L;

c.2606C>T; p.T869M;

c.3040G>A; p.E1014K;

c.816T>C; p.N272N;

c.326G>T; p.G109V;

c.350G>A; p.G117D;

c.4567G>C; p.G1523R;

c.2489G>A; p.G830D;

c.4117C>T; p.R1373C;

c.4842C>A; p.P1614P;

c.2593C>T; p.P865S;

c.1771C>T; p.P591S;

c.2920C>T; p.P974S;

c.3002C>T; p.S1001L;

c.3350C>T; p.P1117L;

c.4475delC; p.L1493fs*101;

c.2923G>A; p.D975N;

c.617C>A; p.A206E;

c.5285G>A; p.R1762H;