ttype patient gene classification type chr pos ref_allele newbase context65 cons46 ESO ESO-1608 DPAGT1 SNP Silent 11 118967924 G A 45 61 LUAD LUAD-RT-S01707 DPAGT1 SNP Splice_site 11 118971846 G A 47 94 LUSC TCGA-22-5489 DPAGT1 SNP Silent 11 118971749 A G 14 54 OV TCGA-24-2293 DPAGT1 SNP Missense_Mutation 11 118971415 A G 1 90 LUAD TCGA-38-4628 DPAGT1 SNP Silent 11 118971518 G A 34 81 LUAD TCGA-38-6178 DPAGT1 SNP Splice_Site 11 118971727 C A 20 93 LUAD TCGA-55-1592 DPAGT1 SNP Silent 11 118971090 C A 25 77 UCEC TCGA-A5-A0G5 DPAGT1 SNP Silent 11 118969160 G A 45 56 BRCA TCGA-A8-A097 DPAGT1 DEL Frame_Shift_Del 11 118967894 G - 47 56 CRC TCGA-AA-3710 DPAGT1 SNP Missense_Mutation 11 118968599 G A 46 87 CRC TCGA-AA-A010 DPAGT1 SNP Silent 11 118971500 G A 34 64 CRC TCGA-AG-A00C DPAGT1 SNP Missense_Mutation 11 118971067 G C 42 99 UCEC TCGA-AX-A0J0 DPAGT1 SNP Missense_Mutation 11 118972310 A G 7 69 UCEC TCGA-B5-A0JY DPAGT1 SNP Missense_Mutation 11 118971797 G T 33 81 KIRC TCGA-B8-5163 DPAGT1 INS Frame_Shift_Ins 11 118972218 - G 55 48 BRCA TCGA-BH-A0E0 DPAGT1 SNP Missense_Mutation 11 118967995 G A 35 72 KIRC TCGA-CJ-5683 DPAGT1 SNP Missense_Mutation 11 118968667 C T 28 100 HNSC TCGA-CN-4723 DPAGT1 INS Frame_Shift_Ins 11 118971068 - A 25 99 UCEC TCGA-D1-A16X DPAGT1 SNP Missense_Mutation 11 118971049 C T 30 99