ttype patient gene classification type chr pos ref_allele newbase context65 cons46 BRCA BR-MEX-193 SNX32 SNP Silent 11 65616954 C T 24 59 CLL CW232 SNX32 SNP Silent 11 65618537 C T 20 51 ESO ESO-155 SNX32 SNP Missense_Mutation 11 65618232 G T 39 79 HNSC HN_62421 SNX32 SNP Missense 11 65617045 C G 29 77 MEL ME021 SNX32 SNP Silent 11 65617707 G A 43 60 MEL MEL-Ma-Mel-105 SNX32 SNP Silent 11 65620119 C T 28 52 MM MM-0465 SNX32 SNP Missense_Mutation 11 65617942 G A 37 78 LUAD TCGA-05-4417 SNX32 SNP Missense_Mutation 11 65620114 G A 39 62 GBM TCGA-06-6388 SNX32 INS Splice_Site 11 65617743 - T 40 71 LUSC TCGA-18-5592 SNX32 SNP Missense_Mutation 11 65618619 C T 27 56 LUSC TCGA-34-5928 SNX32 SNP Silent 11 65618269 G C 45 60 LUSC TCGA-46-6026 SNX32 SNP Missense_Mutation 11 65617738 G A 41 92 LUAD TCGA-55-1595 SNX32 SNP Missense_Mutation 11 65618622 G C 38 54 LUSC TCGA-60-2710 SNX32 SNP Missense_Mutation 11 65620388 A C 9 83 LUSC TCGA-63-6202 SNX32 SNP Silent 11 65620199 C T 23 8 LUAD TCGA-73-4658 SNX32 SNP Missense_Mutation 11 65617697 C G 32 70 CRC TCGA-AA-3516 SNX32 SNP Missense_Mutation 11 65618270 A G 11 74 CRC TCGA-AA-3715 SNX32 SNP Silent 11 65617468 C A 24 52 CRC TCGA-AA-A010 SNX32 SNP Missense_Mutation 11 65618622 G A 38 54 CRC TCGA-AG-A002 SNX32 SNP Missense_Mutation 11 65620387 G T 33 59 BRCA TCGA-AN-A0AL SNX32 SNP Missense_Mutation 11 65617722 G C 33 52 UCEC TCGA-AP-A056 SNX32 SNP Missense_Mutation 11 65617981 C T 27 54 UCEC TCGA-AP-A0LM SNX32 SNP Missense_Mutation 11 65617660 A G 11 40 UCEC TCGA-AX-A0J0 SNX32 SNP Missense_Mutation 11 65620387 G T 33 59 UCEC TCGA-AX-A0J1 SNX32 SNP Silent 11 65616954 C A 24 59 UCEC TCGA-B5-A0JY SNX32 SNP Missense_Mutation 11 65620387 G T 33 59 UCEC TCGA-B5-A11N SNX32 SNP Silent 11 65617947 C A 32 54 UCEC TCGA-B5-A11N SNX32 SNP Missense_Mutation 11 65620383 G A 37 71 UCEC TCGA-BG-A0MG SNX32 SNP Missense_Mutation 11 65618530 T C 59 68 UCEC TCGA-BS-A0UV SNX32 SNP Missense_Mutation 11 65618540 C A 32 93 BLCA TCGA-C4-A0EZ SNX32 SNP Missense_Mutation 11 65618824 C G 32 58 HNSC TCGA-CR-7388 SNX32 SNP Silent 11 65617935 G A 37 37 KIRC TCGA-CZ-4866 SNX32 SNP Missense_Mutation 11 65617711 G C 33 79 UCEC TCGA-D1-A177 SNX32 SNP Missense_Mutation 11 65618804 G A 42 96 UCEC TCGA-D1-A17Q SNX32 SNP Missense_Mutation 11 65618832 C T 27 62 BRCA TCGA-D8-A1JL SNX32 SNP Missense_Mutation 11 65620233 G A 37 81 BLCA TCGA-DK-A3IL SNX32 SNP Missense_Mutation 11 65617466 G T 46 53 BRCA TCGA-E2-A1LA SNX32 SNP Missense_Mutation 11 65620794 G C 35 50