ttype patient gene classification type chr pos ref_allele newbase context65 cons46 CLL CW227 ECM2 SNP Missense_Mutation 9 95277083 C A 30 72 HNSC HN_62237 ECM2 SNP Missense 9 95277270 A G 12 51 LUAD LUAD-E00897 ECM2 SNP Silent 9 95264866 G A 45 54 LUAD LUAD-E00934 ECM2 SNP Missense_Mutation 9 95280005 G T 44 92 MEL MEL-JWCI-WGS-1 ECM2 SNP Missense_Mutation 9 95267864 C T 30 75 MEL MEL-JWCI-WGS-38 ECM2 SNP Missense_Mutation 9 95285109 T G 51 43 MEL MEL-Ma-Mel-102 ECM2 DNP Nonsense_Mutation 9 95277180 GG AA 47 66 MEL MEL-Ma-Mel-35 ECM2 SNP Splice_Site 9 95274292 C T 18 94 MEL MEL-Ma-Mel-67 ECM2 SNP Missense_Mutation 9 95272196 C T 29 67 LUAD TCGA-05-4396 ECM2 SNP Missense_Mutation 9 95267944 C A 21 60 LUAD TCGA-05-4396 ECM2 SNP Silent 9 95279976 G T 39 46 LUSC TCGA-21-1076 ECM2 SNP Missense_Mutation 9 95274313 T C 51 66 LUSC TCGA-22-4599 ECM2 SNP Missense_Mutation 9 95279975 C A 27 55 GBM TCGA-27-2524 ECM2 SNP Missense_Mutation 9 95263237 A G 4 89 LUSC TCGA-33-4547 ECM2 SNP Silent 9 95264875 G C 47 50 LUSC TCGA-37-3789 ECM2 SNP Missense_Mutation 9 95256390 G A 45 49 LUAD TCGA-38-4625 ECM2 SNP Silent 9 95285068 C T 30 57 LUAD TCGA-38-4626 ECM2 SNP Missense_Mutation 9 95272247 A G 12 53 LUAD TCGA-38-4631 ECM2 SNP Missense_Mutation 9 95263280 G T 33 69 OV TCGA-57-1582 ECM2 SNP Nonsense_Mutation 9 95277072 G A 39 53 CRC TCGA-A6-3808 ECM2 SNP Missense_Mutation 9 95263043 G T 36 54 CRC TCGA-AA-3811 ECM2 SNP Missense_Mutation 9 95276973 C T 27 60 CRC TCGA-AA-3821 ECM2 SNP Silent 9 95277256 C T 26 46 CRC TCGA-AA-A00N ECM2 SNP Missense_Mutation 9 95258609 T G 64 70 AML TCGA-AB-2813 ECM2 SNP Missense_Mutation 9 95279998 C T 22 92 CRC TCGA-AG-A015 ECM2 SNP Missense_Mutation 9 95277476 G T 33 50 KIRC TCGA-AK-3425 ECM2 SNP Missense_Mutation 9 95267851 A T 13 50 BRCA TCGA-AO-A0J9 ECM2 SNP Missense_Mutation 9 95277306 C G 32 49 BRCA TCGA-AO-A125 ECM2 DEL In_Frame_Del 9 95277299 TCT - 50 59 UCEC TCGA-AP-A059 ECM2 SNP Missense_Mutation 9 95284931 T C 50 66 UCEC TCGA-AP-A0LM ECM2 SNP Missense_Mutation 9 95263014 C A 32 60 UCEC TCGA-AP-A0LM ECM2 SNP Missense_Mutation 9 95264855 A G 14 63 UCEC TCGA-AP-A0LM ECM2 SNP Nonsense_Mutation 9 95277084 C A 24 71 UCEC TCGA-AX-A05Z ECM2 SNP Missense_Mutation 9 95274321 G T 33 94 UCEC TCGA-AX-A05Z ECM2 SNP Missense_Mutation 9 95284971 C A 20 48 KIRC TCGA-B0-5099 ECM2 SNP Missense_Mutation 9 95272275 A C 4 48 UCEC TCGA-B5-A0JY ECM2 SNP Silent 9 95263287 C T 19 48 UCEC TCGA-B5-A0JY ECM2 SNP Nonsense_Mutation 9 95272235 C A 32 95 BRCA TCGA-B6-A0IK ECM2 SNP Missense_Mutation 9 95277170 C T 27 51 UCEC TCGA-BS-A0TC ECM2 SNP Missense_Mutation 9 95277345 T G 64 66 UCEC TCGA-BS-A0UF ECM2 SNP Missense_Mutation 9 95280056 G T 33 53 UCEC TCGA-BS-A0UV ECM2 SNP Silent 9 95272313 G A 33 68 BLCA TCGA-BT-A20N ECM2 SNP Missense_Mutation 9 95285103 G C 45 60 BLCA TCGA-BT-A20T ECM2 SNP Silent 9 95274343 G A 33 60 BRCA TCGA-C8-A12P ECM2 SNP Missense_Mutation 9 95263288 G A 39 83 HNSC TCGA-CN-6995 ECM2 SNP Missense_Mutation 9 95274325 T A 59 61 HNSC TCGA-CR-7383 ECM2 SNP Missense_Mutation 9 95280053 A T 5 84 HNSC TCGA-CV-6441 ECM2 SNP Missense_Mutation 9 95256393 C T 32 46 UCEC TCGA-D1-A103 ECM2 SNP Missense_Mutation 9 95267838 G T 46 97 UCEC TCGA-D1-A103 ECM2 SNP Nonsense_Mutation 9 95272235 C A 32 95 UCEC TCGA-D1-A103 ECM2 SNP Silent 9 95277031 G A 46 54 BRCA TCGA-D8-A1J9 ECM2 SNP Missense_Mutation 9 95277329 G A 33 50 BLCA TCGA-DK-A3IS ECM2 SNP Missense_Mutation 9 95277062 G C 33 70