ttype patient gene classification type chr pos ref_allele newbase context65 cons46 ESO ESO-0053 SEPT11 SNP Missense_Mutation 4 77941660 A T 9 88 LUAD LUAD-B00416 SEPT11 SNP Nonsense_Mutation 4 77917590 C T 31 83 MEL ME043 SEPT11 DNP Missense_Mutation 4 77940396 CC TT 22 97 MEL MEL-JWCI-WGS-3 SEPT11 SNP Silent 4 77941659 G A 33 56 MEL MEL-JWCI-WGS-34 SEPT11 SNP Silent 4 77941683 G A 45 55 MEL MEL-Ma-Mel-85 SEPT11 SNP Silent 4 77933041 G A 47 56 MEL MEL-Ma-Mel-94 SEPT11 SNP Missense_Mutation 4 77917614 G A 48 98 MM MM-0604 SEPT11 SNP Missense_Mutation 4 77936031 C A 25 98 GBM TCGA-06-2564 SEPT11 SNP Missense_Mutation 4 77949846 G A 33 99 LUAD TCGA-17-Z031 SEPT11 SNP Missense_Mutation 4 77952117 A C 3 77 LUAD TCGA-50-6590 SEPT11 SNP Splice_Site 4 77917577 G A 33 83 CRC TCGA-AA-3977 SEPT11 SNP Missense_Mutation 4 77917670 C A 32 80 CRC TCGA-AA-A00J SEPT11 SNP Missense_Mutation 4 77936159 G A 38 67 CRC TCGA-AA-A01R SEPT11 SNP Nonsense_Mutation 4 77941690 C T 31 63 UCEC TCGA-AP-A051 SEPT11 SNP Missense_Mutation 4 77933061 A G 3 87 UCEC TCGA-AP-A059 SEPT11 SNP Missense_Mutation 4 77940334 C T 25 97 UCEC TCGA-AP-A0LM SEPT11 SNP Missense_Mutation 4 77932959 G A 40 94 UCEC TCGA-AP-A0LM SEPT11 SNP Missense_Mutation 4 77951942 G A 37 99 UCEC TCGA-AX-A1C7 SEPT11 SNP Silent 4 77936125 T C 62 54 KIRC TCGA-B0-4818 SEPT11 SNP Missense_Mutation 4 77949832 A G 7 91 KIRC TCGA-B0-5697 SEPT11 SNP Silent 4 77941776 T G 63 43 UCEC TCGA-B5-A11E SEPT11 SNP Splice_site 4 77955651 G A 46 73 UCEC TCGA-BG-A0VZ SEPT11 SNP Missense_Mutation 4 77932928 G A 42 69 KIRC TCGA-BP-5200 SEPT11 SNP Missense_Mutation 4 77932908 A G 16 73 UCEC TCGA-BS-A0UV SEPT11 SNP Missense_Mutation 4 77926927 G T 33 97 BLCA TCGA-DK-A2I1 SEPT11 SNP Missense_Mutation 4 77926942 G A 33 97 BLCA TCGA-G2-A3IE SEPT11 SNP Missense_Mutation 4 77917662 C G 29 98