ttype patient gene classification type chr pos ref_allele newbase context65 cons46 DLBCL DLBCL-Ls1668 CCM2 SNP Missense_Mutation 7 45104233 G T 44 76 ESO ESO-2143 CCM2 SNP Missense_Mutation 7 45103533 C T 19 72 HNSC HN_62421 CCM2 SNP Missense 7 45113908 G C 46 85 HNSC HN_62421 CCM2 SNP Nonsense 7 45115618 G T 45 81 MEL MEL-JWCI-27 CCM2 SNP Missense_Mutation 7 45103556 C T 30 93 MEL MEL-JWCI-WGS-32 CCM2 SNP Missense_Mutation 7 45115603 A T 8 87 MEL MEL-JWCI-WGS-32 CCM2 SNP Silent 7 45115605 C T 29 72 LUAD TCGA-05-4432 CCM2 SNP Missense_Mutation 7 45108125 G A 46 68 LUAD TCGA-17-Z061 CCM2 SNP Missense_Mutation 7 45077868 C T 21 82 LUSC TCGA-18-3419 CCM2 SNP Missense_Mutation 7 45115438 G T 47 74 LUSC TCGA-33-4586 CCM2 SNP Missense_Mutation 7 45113071 A G 4 47 LUSC TCGA-34-2596 CCM2 SNP Missense_Mutation 7 45113885 C T 29 98 LUSC TCGA-43-3394 CCM2 SNP Missense_Mutation 7 45103574 A G 4 65 LUSC TCGA-46-3765 CCM2 SNP Nonsense_Mutation 7 45112369 G T 41 95 LUAD TCGA-50-6593 CCM2 SNP Silent 7 45104118 G C 48 56 CRC TCGA-AA-3864 CCM2 SNP Missense_Mutation 7 45103533 C T 19 72 CRC TCGA-AG-A014 CCM2 INS In_Frame_Ins 7 45109445 - TGG 28 65 CRC TCGA-AG-A014 CCM2 DEL Frame_Shift_Del 7 45109449 C - 32 96 UCEC TCGA-AP-A051 CCM2 SNP Missense_Mutation 7 45113873 G A 38 70 UCEC TCGA-AP-A0LM CCM2 SNP Silent 7 45115611 C T 27 43 UCEC TCGA-AX-A0J1 CCM2 SNP Missense_Mutation 7 45077975 C T 27 81 UCEC TCGA-B5-A0JR CCM2 SNP Nonsense_Mutation 7 45104092 C T 29 61 UCEC TCGA-B5-A11E CCM2 SNP Silent 7 45104116 C T 24 60 UCEC TCGA-BS-A0UM CCM2 SNP Silent 7 45109499 T C 62 51 UCEC TCGA-BS-A0UV CCM2 SNP Missense_Mutation 7 45109432 C T 27 96 BLCA TCGA-BT-A3PH CCM2 SNP Silent 7 45115443 G A 45 54 KIRC TCGA-CJ-4886 CCM2 SNP Missense_Mutation 7 45113122 C A 27 34 HNSC TCGA-CR-6484 CCM2 SNP Missense_Mutation 7 45113081 G A 48 51 KIRC TCGA-DV-5574 CCM2 SNP Missense_Mutation 7 45067353 T G 52 39 BRCA TCGA-E2-A1II CCM2 SNP Missense_Mutation 7 45113873 G A 38 70