ttype patient gene classification type chr pos ref_allele newbase context65 cons46 BRCA BR-0014 EIF4G2 SNP Silent 11 10824788 T C 52 59 ESO ESO-1060 EIF4G2 SNP Missense_Mutation 11 10825100 A C 8 94 ESO ESO-191 EIF4G2 SNP Silent 11 10827501 G A 39 72 ESO ESO-539 EIF4G2 SNP Silent 11 10823243 G T 37 100 ESO ESO-R61 EIF4G2 SNP Silent 11 10825482 A C 13 73 HNSC HN_62624 EIF4G2 SNP Missense 11 10824787 A T 4 67 HNSC HN_62897 EIF4G2 SNP Nonsense 11 10823724 G A 47 99 LUAD LUAD-RT-S01707 EIF4G2 SNP Silent 11 10821245 G A 33 79 MEL ME009 EIF4G2 SNP Silent 11 10822572 G A 43 60 MEL ME045 EIF4G2 SNP Missense_Mutation 11 10820937 G A 43 73 MEL MEL-13456 EIF4G2 SNP Missense_Mutation 11 10821256 C T 22 87 MEL MEL-JWCI-27 EIF4G2 SNP Silent 11 10826484 G A 45 75 MEL MEL-JWCI-WGS-13 EIF4G2 SNP Missense_Mutation 11 10820565 G A 41 100 MEL MEL-Ma-Mel-79 EIF4G2 SNP Missense_Mutation 11 10823667 G A 47 99 MM MM-0509 EIF4G2 SNP Silent 11 10826511 G A 41 87 MEL Mel_BRAFi_02_PRE EIF4G2 SNP Silent 11 10821848 G A 41 64 LUAD TCGA-05-4389 EIF4G2 SNP Silent 11 10821641 G C 41 43 LUAD TCGA-05-4405 EIF4G2 SNP Silent 11 10822111 G A 36 66 OV TCGA-13-1505 EIF4G2 SNP Missense_Mutation 11 10821215 T G 60 73 LUSC TCGA-18-3406 EIF4G2 SNP Missense_Mutation 11 10822354 G T 47 86 LUSC TCGA-18-4721 EIF4G2 SNP Silent 11 10821167 T C 52 56 LUSC TCGA-22-1011 EIF4G2 SNP Missense_Mutation 11 10820951 C G 20 83 LUSC TCGA-33-4583 EIF4G2 SNP Missense_Mutation 11 10827516 G A 39 100 LUAD TCGA-38-4631 EIF4G2 SNP Silent 11 10820818 T C 57 49 LUSC TCGA-60-2708 EIF4G2 SNP Silent 11 10825569 G A 41 59 UCEC TCGA-A5-A0VP EIF4G2 SNP Nonsense_Mutation 11 10822544 G A 48 91 CRC TCGA-AA-3811 EIF4G2 SNP Nonsense_Mutation 11 10827530 G A 40 100 CRC TCGA-AA-3947 EIF4G2 SNP Missense_Mutation 11 10821282 C T 27 87 CRC TCGA-AA-3949 EIF4G2 SNP Missense_Mutation 11 10822534 C T 27 91 CRC TCGA-AA-3984 EIF4G2 SNP Missense_Mutation 11 10823939 C T 32 100 CRC TCGA-AA-A00N EIF4G2 SNP Missense_Mutation 11 10823859 T G 49 93 CRC TCGA-AA-A010 EIF4G2 SNP Missense_Mutation 11 10821272 C A 32 79 CRC TCGA-AA-A010 EIF4G2 SNP Missense_Mutation 11 10827515 C T 27 74 KIRC TCGA-AK-3425 EIF4G2 SNP Silent 11 10825488 A C 5 66 UCEC TCGA-AP-A056 EIF4G2 SNP Translation_Start_Site 11 10828919 A C 1 75 UCEC TCGA-AP-A059 EIF4G2 SNP Missense_Mutation 11 10825910 C T 17 100 UCEC TCGA-AP-A0LT EIF4G2 SNP Missense_Mutation 11 10823260 G A 37 98 BRCA TCGA-AR-A250 EIF4G2 SNP Missense_Mutation 11 10824832 C A 30 100 KIRC TCGA-B0-4849 EIF4G2 SNP Nonsense_Mutation 11 10825559 C A 30 100 BRCA TCGA-B6-A0RE EIF4G2 SNP Missense_Mutation 11 10827548 G A 41 100 KIRC TCGA-BP-4999 EIF4G2 SNP Missense_Mutation 11 10825853 G C 47 100 UCEC TCGA-BS-A0UF EIF4G2 SNP Missense_Mutation 11 10823939 C A 32 100 UCEC TCGA-BS-A0UV EIF4G2 SNP Missense_Mutation 11 10821810 C T 19 100 BLCA TCGA-BT-A20J EIF4G2 SNP Missense_Mutation 11 10820632 G C 33 60 BLCA TCGA-BT-A20J EIF4G2 SNP Missense_Mutation 11 10820954 G A 33 76 BLCA TCGA-BT-A20J EIF4G2 SNP Missense_Mutation 11 10821742 G T 41 100 BLCA TCGA-BT-A20J EIF4G2 SNP Missense_Mutation 11 10825066 C T 29 100 BLCA TCGA-BT-A20O EIF4G2 SNP Silent 11 10821761 T C 53 67 BLCA TCGA-BT-A20P EIF4G2 SNP Silent 11 10821251 C G 29 51 HNSC TCGA-CN-4734 EIF4G2 SNP Missense_Mutation 11 10821202 T C 52 92 HNSC TCGA-CR-6491 EIF4G2 SNP Silent 11 10825924 C A 17 59 HNSC TCGA-CV-6961 EIF4G2 SNP Missense_Mutation 11 10828424 G C 37 87 HNSC TCGA-CV-7247 EIF4G2 DEL Frame_Shift_Del 11 10821256 CCTTT - 22 87 KIRC TCGA-CZ-5457 EIF4G2 SNP Missense_Mutation 11 10820873 A G 15 78 UCEC TCGA-D1-A17Q EIF4G2 SNP Nonsense_Mutation 11 10819386 C A 32 100 UCEC TCGA-DI-A1NN EIF4G2 SNP Missense_Mutation 11 10823295 C G 32 100 BLCA TCGA-DK-A1AC EIF4G2 SNP Silent 11 10822517 G A 33 61 BLCA TCGA-DK-A2I4 EIF4G2 SNP Silent 11 10823911 G A 45 50 BLCA TCGA-G2-A2EO EIF4G2 DEL Frame_Shift_Del 11 10823639 TG - 63 81 BLCA TCGA-G2-A3IE EIF4G2 SNP Silent 11 10821737 G C 33 64