ttype patient gene classification type chr pos ref_allele newbase context65 cons46 ESO ESO-007 VPS33B SNP Missense_Mutation 15 91561092 G T 45 60 ESO ESO-0167 VPS33B SNP Splice_Site 15 91548923 C T 19 96 ESO ESO-837 VPS33B SNP Silent 15 91557064 G T 46 49 MEL MEL-JWCI-WGS-13 VPS33B SNP Missense_Mutation 15 91550218 C T 31 82 MEL MEL-Ma-Mel-65 VPS33B SNP Missense_Mutation 15 91542939 A C 12 87 LUAD TCGA-05-4396 VPS33B SNP Missense_Mutation 15 91548939 G T 39 96 LUAD TCGA-17-Z022 VPS33B SNP Missense_Mutation 15 91550237 C A 30 72 OV TCGA-24-1417 VPS33B SNP Silent 15 91548135 G C 45 53 LUAD TCGA-44-3919 VPS33B DEL In_Frame_Del 15 91548651 TTC - 64 88 LUSC TCGA-60-2713 VPS33B SNP Nonsense_Mutation 15 91550786 C T 30 95 CRC TCGA-A6-2676 VPS33B SNP Missense_Mutation 15 91561076 T C 51 80 CRC TCGA-AA-A00N VPS33B SNP Missense_Mutation 15 91543787 A G 6 69 UCEC TCGA-AP-A051 VPS33B SNP Missense_Mutation 15 91543778 T C 58 90 UCEC TCGA-AP-A051 VPS33B SNP Nonsense_Mutation 15 91549655 C A 32 93 UCEC TCGA-AX-A05Z VPS33B SNP Missense_Mutation 15 91544668 G T 33 98 UCEC TCGA-B5-A0JR VPS33B SNP Splice_Site 15 91543024 C A 32 87 UCEC TCGA-B5-A0JY VPS33B SNP Missense_Mutation 15 91548976 G T 37 48 UCEC TCGA-BS-A0TC VPS33B SNP Missense_Mutation 15 91544668 G A 33 98 UCEC TCGA-BS-A0UV VPS33B SNP Missense_Mutation 15 91553074 G T 33 53 BRCA TCGA-C8-A1HI VPS33B SNP Missense_Mutation 15 91551102 G C 33 74 HNSC TCGA-CN-5355 VPS33B SNP Nonsense_Mutation 15 91557072 G A 39 53 HNSC TCGA-CV-7177 VPS33B SNP Missense_Mutation 15 91544674 A C 9 90 HNSC TCGA-CV-7407 VPS33B SNP Missense_Mutation 15 91557634 T C 56 53 UCEC TCGA-D1-A103 VPS33B SNP Splice_site 15 91548926 A G 11 88 UCEC TCGA-D1-A103 VPS33B SNP Missense_Mutation 15 91548963 G T 34 82 UCEC TCGA-D1-A160 VPS33B SNP Silent 15 91543804 G A 38 49 UCEC TCGA-D1-A17Q VPS33B SNP Silent 15 91553038 G T 33 64 UCEC TCGA-D1-A17U VPS33B SNP Missense_Mutation 15 91543727 A G 4 90 HNSC TCGA-DQ-5629 VPS33B SNP Nonsense_Mutation 15 91546342 G T 44 54 BRCA TCGA-E9-A1R4 VPS33B SNP Missense_Mutation 15 91550259 C G 30 95 BRCA TCGA-EW-A1PB VPS33B SNP Missense_Mutation 15 91561082 C G 32 86 HNSC TCGA-H7-7774 VPS33B SNP Missense_Mutation 15 91542965 G C 33 73