ttype patient gene classification type chr pos ref_allele newbase context65 cons46 LUAD LUAD-D02085 ALDOB SNP Missense_Mutation 9 104189825 G A 41 87 MEL MEL-JWCI-WGS-32 ALDOB SNP Missense_Mutation 9 104187762 G A 47 56 MEL MEL-JWCI-WGS-33 ALDOB SNP Missense_Mutation 9 104189919 C T 29 100 MEL MEL-JWCI-WGS-7 ALDOB SNP Silent 9 104187200 G A 47 77 MEL MEL-JWCI-WGS-7 ALDOB SNP Silent 9 104192238 C T 30 42 LUAD TCGA-05-4249 ALDOB SNP Missense_Mutation 9 104189921 A T 3 93 LUAD TCGA-05-4405 ALDOB SNP Nonsense_Mutation 9 104189909 G C 45 87 GBM TCGA-06-0216 ALDOB SNP Missense_Mutation 9 104187273 A T 11 92 LUAD TCGA-64-5779 ALDOB SNP Missense_Mutation 9 104189769 G T 45 100 LUSC TCGA-66-2759 ALDOB SNP Missense_Mutation 9 104193079 G T 35 71 LUSC TCGA-66-2766 ALDOB SNP Missense_Mutation 9 104192152 A G 12 92 LUAD TCGA-91-6831 ALDOB DEL Frame_Shift_Del 9 104190767 TTTG - 56 51 CRC TCGA-A6-2676 ALDOB SNP Splice_site 9 104189764 C A 24 100 CRC TCGA-AA-3821 ALDOB SNP Missense_Mutation 9 104187180 C G 18 51 CRC TCGA-AA-3845 ALDOB SNP Missense_Mutation 9 104189822 C A 28 54 CRC TCGA-AA-3949 ALDOB SNP Missense_Mutation 9 104187208 G T 35 100 CRC TCGA-AA-A010 ALDOB SNP Silent 9 104192139 G A 37 43 CRC TCGA-AA-A01Q ALDOB SNP Missense_Mutation 9 104189817 C T 27 100 BRCA TCGA-AN-A04C ALDOB SNP Missense_Mutation 9 104184143 G A 33 65 UCEC TCGA-AP-A051 ALDOB SNP Missense_Mutation 9 104189780 G T 42 100 UCEC TCGA-AP-A056 ALDOB SNP Missense_Mutation 9 104193159 C T 31 50 UCEC TCGA-AP-A05N ALDOB SNP Nonsense_Mutation 9 104189860 C T 26 100 UCEC TCGA-AP-A0LM ALDOB SNP Missense_Mutation 9 104187133 G A 38 70 UCEC TCGA-AP-A0LM ALDOB SNP Missense_Mutation 9 104187845 T G 56 92 UCEC TCGA-AP-A0LM ALDOB SNP Missense_Mutation 9 104192195 G A 39 100 UCEC TCGA-AX-A0J0 ALDOB SNP Nonsense_Mutation 9 104187236 C T 30 100 UCEC TCGA-AX-A0J1 ALDOB SNP Missense_Mutation 9 104193159 C T 31 50 KIRC TCGA-B0-5711 ALDOB INS Frame_Shift_Ins 9 104187311 - A 17 64 KIRC TCGA-B0-5812 ALDOB DEL Frame_Shift_Del 9 104190767 TTTG - 56 51 UCEC TCGA-B5-A11E ALDOB SNP Missense_Mutation 9 104187223 A G 11 92 UCEC TCGA-B5-A11E ALDOB SNP Silent 9 104189911 G A 33 55 KIRC TCGA-B8-5164 ALDOB SNP Silent 9 104192184 G A 41 70 UCEC TCGA-BG-A18B ALDOB SNP Missense_Mutation 9 104193145 T C 59 67 BLCA TCGA-BL-A13J ALDOB SNP Silent 9 104192127 G A 41 72 KIRC TCGA-BP-5200 ALDOB SNP Silent 9 104187208 G A 35 100 BRCA TCGA-C8-A1HG ALDOB SNP Missense_Mutation 9 104193120 G A 45 86 HNSC TCGA-CN-4723 ALDOB SNP Missense_Mutation 9 104192167 G A 33 61 HNSC TCGA-CR-7388 ALDOB SNP Missense_Mutation 9 104187801 T A 57 70 HNSC TCGA-CR-7395 ALDOB SNP Missense_Mutation 9 104187258 A C 3 57 KIRC TCGA-CZ-5465 ALDOB INS Frame_Shift_Ins 9 104192206 - TT 36 70 UCEC TCGA-D1-A103 ALDOB SNP Missense_Mutation 9 104187224 G T 33 71 BLCA TCGA-FD-A3N6 ALDOB SNP Missense_Mutation 9 104189787 G A 37 85