ttype patient gene classification type chr pos ref_allele newbase context65 cons46 DLBCL DLBCL-LS4616 WT1 SNP Missense_Mutation 11 32439142 A C 3 53 ESO ESO-185 WT1 SNP Missense_Mutation 11 32456375 C T 23 73 LUAD LUAD-S01315 WT1 SNP Missense_Mutation 11 32450124 G A 45 98 LUAD LUAD-TLLGS WT1 SNP Splice_site 11 32421496 G A 45 99 MEL MEL-JWCI-WGS-1 WT1 DNP Missense_Mutation 11 32417914 GT CG 40 59 MEL MEL-JWCI-WGS-6 WT1 SNP Missense_Mutation 11 32439146 C T 29 88 MEL MEL-Ma-Mel-67 WT1 SNP Nonsense_Mutation 11 32413596 G A 47 88 MEL MEL-Ma-Mel-67 WT1 SNP Missense_Mutation 11 32417853 T C 56 94 MEL MEL-Ma-Mel-94 WT1 SNP Missense_Mutation 11 32438075 C T 22 76 MM MM-0501 WT1 DNP Splice_Site 11 32439122 CC TA 18 88 NB NB-1942 WT1 SNP Missense_Mutation 11 32410674 C G 23 100 LUAD TCGA-05-4382 WT1 SNP Missense_Mutation 11 32413568 G A 41 89 LUAD TCGA-05-4396 WT1 SNP Silent 11 32413566 G T 39 70 LUAD TCGA-05-5425 WT1 SNP Missense_Mutation 11 32456435 C T 31 88 GBM TCGA-12-0615 WT1 SNP Missense_Mutation 11 32450114 G A 37 98 LUAD TCGA-17-Z030 WT1 SNP Splice_Site 11 32413611 C A 24 100 LUAD TCGA-17-Z055 WT1 SNP Silent 11 32414252 A G 11 60 GBM TCGA-27-2528 WT1 SNP Nonsense_Mutation 11 32413578 G A 38 67 LUSC TCGA-34-2596 WT1 SNP Missense_Mutation 11 32456334 G C 42 61 LUSC TCGA-34-5232 WT1 SNP Silent 11 32450095 G A 41 50 LUSC TCGA-43-6647 WT1 SNP Silent 11 32439176 G T 43 52 LUSC TCGA-46-3769 WT1 SNP Silent 11 32417924 C A 31 27 LUSC TCGA-46-3769 WT1 SNP Missense_Mutation 11 32450097 A G 2 63 LUAD TCGA-49-4487 WT1 SNP Missense_Mutation 11 32450106 C A 25 64 LUAD TCGA-49-4505 WT1 SNP Missense_Mutation 11 32414287 G T 47 100 LUAD TCGA-50-5941 WT1 SNP Missense_Mutation 11 32413601 G T 47 100 LUAD TCGA-55-1592 WT1 SNP Splice_site 11 32413610 C A 18 100 LUSC TCGA-60-2719 WT1 SNP Missense_Mutation 11 32421532 A C 16 91 LUAD TCGA-64-5775 WT1 SNP Missense_Mutation 11 32414272 C A 30 100 LUAD TCGA-64-5781 WT1 SNP Missense_Mutation 11 32413565 C A 23 100 LUSC TCGA-66-2727 WT1 SNP Missense_Mutation 11 32439126 T G 56 82 GBM TCGA-76-6660 WT1 SNP Silent 11 32421505 T G 55 64 LUAD TCGA-86-6562 WT1 SNP Silent 11 32456382 G C 46 68 KIRC TCGA-A3-3326 WT1 SNP Missense_Mutation 11 32421532 A T 16 91 CRC TCGA-A6-2672 WT1 SNP Missense_Mutation 11 32413565 C T 23 100 CRC TCGA-AA-3544 WT1 SNP Missense_Mutation 11 32421519 G A 40 99 CRC TCGA-AA-3710 WT1 SNP Silent 11 32410610 C T 27 48 CRC TCGA-AA-3715 WT1 SNP Missense_Mutation 11 32413574 T G 56 72 CRC TCGA-AA-3930 WT1 SNP Missense_Mutation 11 32410683 T C 56 93 CRC TCGA-AA-3941 WT1 SNP Silent 11 32421569 G A 38 40 AML TCGA-AB-2839 WT1 INS Frame_Shift_Ins 11 32417908 - CCGA 26 63 AML TCGA-AB-2844 WT1 INS Frame_Shift_Ins 11 32417910 - ACCGTACA 37 96 AML TCGA-AB-2846 WT1 INS Frame_Shift_Ins 11 32417909 - A 23 24 AML TCGA-AB-2874 WT1 SNP Missense_Mutation 11 32413566 G A 39 70 AML TCGA-AB-2905 WT1 INS Frame_Shift_Ins 11 32417922 - TCGGGGCTAC 36 88 AML TCGA-AB-2913 WT1 SNP Splice_Site 11 32417802 C G 18 100 AML TCGA-AB-2919 WT1 SNP Missense_Mutation 11 32413557 G A 47 100 AML TCGA-AB-2930 WT1 INS Frame_Shift_Ins 11 32417941 - A 17 100 AML TCGA-AB-2970 WT1 SNP Splice_Site 11 32413611 C T 24 100 AML TCGA-AB-2976 WT1 INS Frame_Shift_Ins 11 32417909 - GACCG 23 24 AML TCGA-AB-2989 WT1 DEL Frame_Shift_Del 11 32417846 AT - 4 51 AML TCGA-AB-3009 WT1 INS Frame_Shift_Ins 11 32417909 - GACCG 23 24 CRC TCGA-AF-2692 WT1 SNP Silent 11 32421575 G A 40 44 CRC TCGA-AG-A002 WT1 SNP Missense_Mutation 11 32421570 C T 28 63 CRC TCGA-AG-A02N WT1 SNP Missense_Mutation 11 32450156 G A 40 84 UCEC TCGA-AP-A051 WT1 SNP Silent 11 32450098 C T 20 76 BRCA TCGA-AR-A1AJ WT1 SNP Silent 11 32450119 C T 27 51 UCEC TCGA-B5-A11E WT1 SNP Silent 11 32421518 C T 27 42 UCEC TCGA-BG-A0VW WT1 SNP Missense_Mutation 11 32410656 C T 27 100 BRCA TCGA-BH-A18P WT1 SNP Missense_Mutation 11 32414250 C T 19 100 KIRC TCGA-BP-4803 WT1 DEL Frame_Shift_Del 11 32456513 CC - 26 54 KIRC TCGA-BP-5175 WT1 SNP Missense_Mutation 11 32417899 T A 58 62 UCEC TCGA-BS-A0UV WT1 SNP Missense_Mutation 11 32417914 G A 40 59 BLCA TCGA-BT-A2LB WT1 SNP Splice_site 11 32410605 C G 29 62 BRCA TCGA-C8-A27B WT1 SNP Missense_Mutation 11 32410657 G A 39 100 HNSC TCGA-CV-7427 WT1 SNP Silent 11 32417879 G A 45 70 UCEC TCGA-D1-A167 WT1 SNP Missense_Mutation 11 32413565 C A 23 100