ttype patient gene classification type chr pos ref_allele newbase context65 cons46 HNSC HN_62426 SNX15 SNP Synonymous 11 64802401 C G 29 56 MEL ME009 SNX15 SNP Silent 11 64800007 C T 22 46 MM MM-0191 SNX15 SNP Missense 11 64802425 G C 36 54 LUAD TCGA-05-4415 SNX15 SNP Missense_Mutation 11 64806226 G A 45 72 GBM TCGA-06-0185 SNX15 SNP Missense_Mutation 11 64800008 C T 23 65 OV TCGA-09-0369 SNX15 SNP Missense_Mutation 11 64799920 G T 44 51 LUSC TCGA-18-3409 SNX15 SNP Missense_Mutation 11 64800004 C T 30 56 LUSC TCGA-39-5031 SNX15 SNP Missense_Mutation 11 64803125 C G 32 63 LUAD TCGA-50-5049 SNX15 SNP Splice_site 11 64795011 T C 51 73 LUSC TCGA-66-2755 SNX15 SNP Missense_Mutation 11 64806067 C G 21 59 CRC TCGA-AA-3864 SNX15 SNP Silent 11 64802605 G A 38 36 UCEC TCGA-AP-A059 SNX15 SNP Missense_Mutation 11 64802556 A T 11 62 KIRC TCGA-B0-4690 SNX15 SNP Missense_Mutation 11 64799919 G A 39 83 KIRC TCGA-BP-4807 SNX15 SNP Missense_Mutation 11 64799918 C T 27 70 UCEC TCGA-BS-A0TG SNX15 SNP Nonsense_Mutation 11 64802351 C T 27 58 HNSC TCGA-CR-6492 SNX15 SNP Nonsense_Mutation 11 64802351 C T 27 58 BLCA TCGA-DK-A2I4 SNX15 SNP Missense_Mutation 11 64795031 G A 45 96 HNSC TCGA-DQ-5629 SNX15 SNP Missense_Mutation 11 64795103 G C 38 95 BRCA TCGA-E2-A1LA SNX15 SNP Missense_Mutation 11 64803030 G C 41 86 BRCA TCGA-EW-A1PB SNX15 SNP Missense_Mutation 11 64803125 C A 32 63