ttype patient gene classification type chr pos ref_allele newbase context65 cons46 LUAD LUAD-NYU575 TMOD2 SNP Missense_Mutation 15 52090423 G T 33 59 LUAD LUAD-S01357 TMOD2 SNP Missense_Mutation 15 52074960 G C 41 95 MEL MEL-JWCI-WGS-12 TMOD2 SNP Silent 15 52058723 C T 20 88 MEL MEL-Ma-Mel-122 TMOD2 SNP Missense_Mutation 15 52074925 C T 21 95 MEL MEL-Ma-Mel-65 TMOD2 SNP Missense_Mutation 15 52060595 C T 22 100 LUAD TCGA-05-4396 TMOD2 SNP Missense_Mutation 15 52075002 C A 31 80 OV TCGA-24-2024 TMOD2 DEL Frame_Shift_Del 15 52090499 G - 33 70 OV TCGA-36-1577 TMOD2 SNP Missense_Mutation 15 52058735 G C 41 87 LUSC TCGA-63-5128 TMOD2 SNP Missense_Mutation 15 52098653 A G 14 92 GBM TCGA-76-4932 TMOD2 SNP Missense_Mutation 15 52075020 G C 42 93 LUSC TCGA-85-6560 TMOD2 SNP Missense_Mutation 15 52098581 A C 7 91 CRC TCGA-AA-3672 TMOD2 SNP Nonsense_Mutation 15 52098676 C T 19 58 CRC TCGA-AA-3966 TMOD2 SNP Missense_Mutation 15 52090430 A G 10 62 AML TCGA-AB-2863 TMOD2 SNP Missense_Mutation 15 52060550 T A 55 93 UCEC TCGA-AP-A051 TMOD2 SNP Missense_Mutation 15 52100647 G T 35 61 UCEC TCGA-AX-A0J0 TMOD2 SNP Missense_Mutation 15 52098584 T C 63 91 UCEC TCGA-B5-A11E TMOD2 SNP Missense_Mutation 15 52075002 C T 31 80 UCEC TCGA-BG-A0MQ TMOD2 SNP Missense_Mutation 15 52066008 A G 10 92 KIRC TCGA-BP-5187 TMOD2 SNP Missense_Mutation 15 52065996 C A 26 86 KIRC TCGA-BP-5187 TMOD2 SNP Missense_Mutation 15 52066002 C T 26 100 BLCA TCGA-BT-A0YX TMOD2 SNP Missense_Mutation 15 52069173 G A 45 86 BLCA TCGA-BT-A20R TMOD2 SNP Silent 15 52074980 G A 33 54 BLCA TCGA-BT-A20R TMOD2 SNP Missense_Mutation 15 52075011 G C 45 94 HNSC TCGA-CV-6951 TMOD2 SNP Missense_Mutation 15 52058689 A T 3 52 HNSC TCGA-CV-7427 TMOD2 SNP Silent 15 52069169 C T 31 50 KIRC TCGA-CZ-5461 TMOD2 SNP Nonsense_Mutation 15 52098676 C T 19 58 BLCA TCGA-DK-A3IS TMOD2 SNP Silent 15 52090495 G A 45 52 UCEC TCGA-EY-A1GS TMOD2 SNP Missense_Mutation 15 52098598 G C 33 99