ttype patient gene classification type chr pos ref_allele newbase context65 cons46 ESO ESO-153 TM2D2 SNP Silent 8 38853794 G C 39 50 LUAD TCGA-17-Z031 TM2D2 SNP Silent 8 38848892 G A 34 72 LUAD TCGA-17-Z058 TM2D2 SNP Missense_Mutation 8 38853916 C T 23 81 LUAD TCGA-35-4123 TM2D2 SNP Missense_Mutation 8 38851131 G A 47 48 UCEC TCGA-A5-A0VP TM2D2 SNP Nonsense_Mutation 8 38851086 G A 40 72 CRC TCGA-AA-3955 TM2D2 SNP Missense_Mutation 8 38851152 C G 30 67 CRC TCGA-AA-A00N TM2D2 SNP Missense_Mutation 8 38848996 C T 31 100 CRC TCGA-AA-A010 TM2D2 SNP Missense_Mutation 8 38852976 G A 38 56 BRCA TCGA-AR-A1AH TM2D2 DEL In_Frame_Del 8 38852949 ATC - 12 42 BRCA TCGA-AR-A256 TM2D2 SNP Missense_Mutation 8 38852899 C G 32 98 UCEC TCGA-AX-A0J1 TM2D2 SNP Missense_Mutation 8 38849059 G A 44 87 UCEC TCGA-B5-A0JY TM2D2 SNP Missense_Mutation 8 38852992 T C 57 44 HNSC TCGA-CR-7402 TM2D2 SNP Missense_Mutation 8 38853858 T C 59 60 HNSC TCGA-CV-5442 TM2D2 SNP Missense_Mutation 8 38851142 G A 45 49 KIRC TCGA-DV-5566 TM2D2 SNP Nonsense_Mutation 8 38853913 G A 47 95