ttype patient gene classification type chr pos ref_allele newbase context65 cons46 ESO ESO-0459 PMM2 SNP Missense_Mutation 16 8895737 G C 45 63 LUAD LUAD-CHTN-Z4716A PMM2 SNP Silent 16 8905506 A T 13 61 MEL ME045 PMM2 SNP Missense_Mutation 16 8900254 C T 22 80 OV TCGA-23-2079 PMM2 SNP Silent 16 8895757 G A 47 57 UCEC TCGA-A5-A0VP PMM2 SNP Silent 16 8941640 G A 38 29 CRC TCGA-AA-3554 PMM2 SNP Silent 16 8905023 C T 19 43 UCEC TCGA-AP-A051 PMM2 SNP Missense_Mutation 16 8905009 C T 19 74 UCEC TCGA-AP-A0LM PMM2 SNP Missense_Mutation 16 8900240 C T 27 78 UCEC TCGA-B5-A11H PMM2 SNP Missense_Mutation 16 8898674 A G 5 87 UCEC TCGA-BS-A0TJ PMM2 SNP Nonsense_Mutation 16 8895686 C T 17 77 UCEC TCGA-BS-A0UJ PMM2 SNP Splice_site 16 8898699 A G 7 87 UCEC TCGA-BS-A0UV PMM2 SNP Missense_Mutation 16 8906942 C A 32 78 BLCA TCGA-DK-A1AC PMM2 SNP Silent 16 8941604 C T 29 76 BLCA TCGA-HQ-A2OE PMM2 DEL In_Frame_Del 16 8906913 GAAAAT - 41 91