PCGP germline mutation   [Top]

PCGP somatic mutation   [Top]

COSMIC somatic mutation   [Top]

c.461A>G; p.N154S;

c.4088T>A; p.I1363N;

c.1100C>T; p.P367L;

c.1051C>T; p.P351S;

c.2258delT; p.M753fs*54;

c.1922C>T; p.S641L;

c.3765G>T; p.Q1255H;

c.3305G>A; p.S1102N;

c.2192G>T; p.R731I;

c.1880A>C; p.N627T;

c.814A>C; p.S272R;

c.475G>A; p.E159K;

c.3371C>G; p.S1124C;

c.3676T>A; p.S1226T; 1:198801406-198801406

c.3550T>C; p.S1184P;

c.1426_1427insT; p.S476fs*16;

c.871T>C; p.C291R;

c.140G>T; p.C47F;

c.318G>C; p.E106D;

c.321G>T; p.L107F;

c.3871G>A; p.E1291K;

c.3272C>G; p.S1091*;

c.934C>G; p.Q312E;

c.1371G>T; p.M457I;

c.4808A>T; p.E1603V;

c.1924G>A; p.E642K;

c.4363G>C; p.E1455Q; 1:198791196-198791196

c.4402G>T; p.E1468*; 1:198791157-198791157

c.872G>A; p.C291Y;

c.1090C>T; p.R364C;

c.4868A>G; p.K1623R;

c.812G>C; p.G271A;

c.3191A>C; p.E1064A;

c.1979G>T; p.W660L;

c.4203C>T; p.N1401N;

c.2796C>T; p.L932L;

c.3040G>T; p.A1014S;

c.1368-1G>T; p.?;

c.4818A>T; p.Q1606H;

c.2096G>A; p.R699H; 1:198837703-198837703

c.2096G>A; p.R699H; 1:198837703-198837703

c.1226C>T; p.S409F;

c.4808A>T; p.E1603V;

c.2218C>T; p.R740*;

c.4007G>C; p.R1336T;

c.4007G>C; p.R1336T;

c.1A>G; p.M1V;

c.4539T>A; p.A1513A;

c.3137G>A; p.R1046H;

c.1367+4A>G; p.?;

c.415G>T; p.D139Y;

c.3882T>C; p.D1294D;

c.2219G>A; p.R740Q;

c.2096G>A; p.R699H; 1:198837703-198837703

c.4654C>T; p.P1552S; 1:198789432-198789432

c.3323A>G; p.Y1108C;

c.4410C>G; p.I1470M;

c.1737C>A; p.T579T;

c.3952G>A; p.V1318I;

c.461A>G; p.N154S;

c.2814-1G>A; p.?;

c.3659C>T; p.S1220L;

c.2526G>T; p.G842G;

c.4706A>T; p.Q1569L;

c.2384A>T; p.Q795L;

c.2814-1G>A; p.?;

c.3582G>A; p.M1194I;

c.1603T>A; p.S535T;

c.1185G>A; p.T395T;

c.194G>T; p.R65I;

c.3901C>T; p.R1301*;

c.1185G>A; p.T395T;

c.4654C>T; p.P1552S; 1:198789432-198789432

c.2690G>T; p.R897I;

c.4116G>T; p.K1372N;

c.4186C>T; p.L1396L;

c.4444C>T; p.Q1482*;

c.1793G>A; p.R598Q;

c.1793G>A; p.R598Q;

c.3593G>T; p.R1198I;

c.2311G>T; p.E771*;

c.1406G>T; p.R469I;

c.2136C>T; p.N712N;

c.3678A>G; p.S1226S;

c.4365A>G; p.E1455E;

c.1396A>C; p.I466L;

c.4363G>T; p.E1455*;

c.1793G>A; p.R598Q;

c.1669G>A; p.A557T;

c.3758T>G; p.F1253C;

c.1503A>C; p.K501N;

c.1240C>A; p.H414N;

c.685G>A; p.V229I;

c.2716A>C; p.K906Q;

c.4116G>T; p.K1372N;

c.3103G>A; p.A1035T;

c.194G>T; p.R65I;

c.1184C>T; p.T395M;

c.3215G>A; p.R1072Q;

c.2289A>G; p.A763A;

c.1544G>T; p.R515I;

c.104G>A; p.R35Q;

c.4730C>A; p.S1577Y;

c.2457G>T; p.M819I;

c.4030G>A; p.E1344K;

c.22A>C; p.N8H;

c.16A>G; p.T6A;

c.4656T>C; p.P1552P;

c.1455+1G>A; p.?;

c.988G>A; p.A330T;

c.4474G>T; p.D1492Y;

c.1793G>A; p.R598Q;

c.779G>A; p.G260E;

c.2149A>G; p.R717G;

c.901C>G; p.P301A;

c.1919T>C; p.L640P;

c.1367C>T; p.T456M;

c.944A>T; p.Q315L;

c.2596G>A; p.E866K;

c.3989C>A; p.P1330H;

c.3083G>A; p.R1028Q;

c.3266A>G; p.K1089R;

c.724_725delAG; p.S242fs*15;

c.189A>G; p.I63M;

c.110A>C; p.K37T;

c.366A>G; p.Q122Q;

c.4404A>G; p.E1468E;

c.2022G>C; p.M674I;

c.199T>A; p.Y67N;

c.530C>G; p.S177C;

c.1460G>A; p.S487N;

c.767A>G; p.H256R;

c.3136C>G; p.R1046G;

c.2353A>C; p.K785Q;

c.2225G>A; p.R742K;

c.235C>A; p.P79T;

c.518C>G; p.S173C;

c.2618G>A; p.G873E;

c.1768G>A; p.E590K;

c.1349G>T; p.G450V;

c.692G>C; p.R231T;

c.3678A>G; p.S1226S;

c.2095C>T; p.R699C;

c.4364A>G; p.E1455G;

c.4125C>A; p.I1375I;

c.2374A>T; p.I792F;

c.4364A>G; p.E1455G;

c.3272C>T; p.S1091L;

c.4656T>C; p.P1552P;

c.3049C>A; p.H1017N;

c.4730C>T; p.S1577F;

c.1774G>A; p.D592N;

c.250C>T; p.P84S;

c.4513_4514insCC; p.K1505fs*3;

c.840delA; p.K280fs*8;

c.4349delA; p.N1450fs*7;