ttype patient gene classification type chr pos ref_allele newbase context65 cons46 DLBCL DLBCL-MAYO_DLBCL_234 SIM2 SNP Missense_Mutation 21 38092185 G A 38 84 LUAD LUAD-E00443 SIM2 SNP Silent 21 38098500 G T 47 63 LUAD LUAD-LIP77 SIM2 SNP Missense_Mutation 21 38072183 C A 18 98 LUAD LUAD-LIP77 SIM2 SNP Missense_Mutation 21 38098484 C A 30 87 LUAD LUAD-RT-S01699 SIM2 SNP Missense_Mutation 21 38117215 C G 29 65 LUAD LUAD-S01468 SIM2 SNP Missense_Mutation 21 38081472 A T 15 54 MEL ME009 SIM2 SNP Missense_Mutation 21 38115704 G A 41 80 MEL MEL-JWCI-14 SIM2 SNP Missense_Mutation 21 38117236 C T 26 71 MEL MEL-JWCI-WGS-39 SIM2 SNP Silent 21 38114070 G A 43 48 PRAD P04-1243 SIM2 SNP Silent 21 38117286 G A 47 71 LUAD TCGA-05-4390 SIM2 SNP Missense_Mutation 21 38114105 T C 59 91 LUAD TCGA-17-Z056 SIM2 SNP Missense_Mutation 21 38095399 A G 3 59 LUSC TCGA-56-1622 SIM2 SNP Missense_Mutation 21 38115753 C T 30 60 LUSC TCGA-66-2758 SIM2 SNP Missense_Mutation 21 38072165 C T 27 98 GBM TCGA-76-6192 SIM2 SNP Missense_Mutation 21 38092132 C T 19 97 CRC TCGA-AG-3586 SIM2 SNP Silent 21 38092190 C T 30 44 UCEC TCGA-AP-A0LM SIM2 SNP Silent 21 38095365 G A 40 7 UCEC TCGA-AX-A0J0 SIM2 SNP Silent 21 38072205 C T 27 53 KIRC TCGA-BP-4963 SIM2 SNP Missense_Mutation 21 38084845 T A 52 89 UCEC TCGA-BS-A0UF SIM2 SNP Missense_Mutation 21 38098446 G T 33 87 HNSC TCGA-CN-6011 SIM2 SNP Missense_Mutation 21 38072060 C G 30 74 UCEC TCGA-D1-A17Q SIM2 SNP Nonsense_Mutation 21 38095375 C T 31 67 BRCA TCGA-EW-A1OX SIM2 SNP Nonsense_Mutation 21 38095375 C T 31 67