ttype patient gene classification type chr pos ref_allele newbase context65 cons46 MEL MEL-Ma-Mel-36 ALG2 SNP Silent 9 101980788 G A 35 51 MEL MEL-Ma-Mel-48 ALG2 SNP Missense_Mutation 9 101980664 C T 18 99 MEL MEL-Ma-Mel-67 ALG2 DNP Silent 9 101980728 GG AA 35 53 LUAD TCGA-05-4382 ALG2 SNP Missense_Mutation 9 101980872 G A 35 84 LUAD TCGA-05-4396 ALG2 SNP Silent 9 101980242 G T 39 74 LUAD TCGA-05-4396 ALG2 SNP Missense_Mutation 9 101980370 G T 39 99 LUAD TCGA-05-4396 ALG2 SNP Nonsense_Mutation 9 101980764 C A 31 98 OV TCGA-13-1497 ALG2 SNP Missense_Mutation 9 101980889 T G 59 68 LUAD TCGA-17-Z046 ALG2 DEL Frame_Shift_Del 9 101980734 C - 30 56 LUSC TCGA-18-3416 ALG2 SNP Silent 9 101980729 G A 43 47 OV TCGA-23-2072 ALG2 SNP Nonsense_Mutation 9 101980977 C A 30 97 LUSC TCGA-60-2715 ALG2 SNP Missense_Mutation 9 101981079 G A 38 72 LUAD TCGA-64-1676 ALG2 SNP Missense_Mutation 9 101980430 G A 37 85 LUSC TCGA-66-2773 ALG2 SNP Silent 9 101980675 C G 29 51 LUSC TCGA-66-2795 ALG2 SNP Missense_Mutation 9 101980956 C T 32 97 LUSC TCGA-66-2800 ALG2 SNP Missense_Mutation 9 101984110 C A 32 93 CRC TCGA-AA-3518 ALG2 SNP Missense_Mutation 9 101980931 A T 9 76 CRC TCGA-AA-A00N ALG2 SNP Missense_Mutation 9 101980562 G T 33 99 CRC TCGA-AA-A010 ALG2 SNP Missense_Mutation 9 101980562 G T 33 99 BRCA TCGA-AN-A0AL ALG2 SNP Missense_Mutation 9 101980329 G A 44 99 UCEC TCGA-AP-A0LM ALG2 SNP Missense_Mutation 9 101980452 A G 6 77 UCEC TCGA-AP-A0LM ALG2 SNP Missense_Mutation 9 101981071 C A 32 59 BRCA TCGA-BH-A0W7 ALG2 SNP Missense_Mutation 9 101980615 C A 29 64 KIRC TCGA-BP-4964 ALG2 SNP Splice_Site 9 101983421 T C 55 52 HNSC TCGA-CV-6937 ALG2 SNP Silent 9 101980621 C T 24 51 HNSC TCGA-CV-6951 ALG2 SNP Missense_Mutation 9 101980370 G A 39 99 HNSC TCGA-CV-7104 ALG2 SNP Missense_Mutation 9 101980890 G C 45 68 BLCA TCGA-DK-A1AC ALG2 SNP Silent 9 101980576 C T 29 57 BLCA TCGA-DK-A1AE ALG2 SNP Missense_Mutation 9 101984145 G A 37 45 BLCA TCGA-GD-A2C5 ALG2 SNP Missense_Mutation 9 101980827 C T 29 73