ttype patient gene classification type chr pos ref_allele newbase context65 cons46 ESO ESO-1733 P2RY6 SNP Silent 11 73007833 T C 50 62 LUAD LUAD-B00416 P2RY6 SNP Nonsense_Mutation 11 73008494 C T 27 70 LUAD LUAD-RT-S01709 P2RY6 SNP Silent 11 73007729 C A 23 63 MEL ME009 P2RY6 SNP Silent 11 73008460 C T 30 53 MEL ME043 P2RY6 SNP Nonsense_Mutation 11 73007662 T A 52 64 LUAD TCGA-05-4396 P2RY6 SNP Missense_Mutation 11 73007955 C A 23 95 OV TCGA-13-1497 P2RY6 SNP Missense_Mutation 11 73008401 G T 46 70 LUAD TCGA-49-4488 P2RY6 SNP Silent 11 73008427 G A 40 57 LUAD TCGA-50-5930 P2RY6 SNP Missense_Mutation 11 73008276 C T 26 70 LUAD TCGA-50-5939 P2RY6 SNP Silent 11 73007896 C T 19 52 LUSC TCGA-70-6722 P2RY6 SNP Missense_Mutation 11 73007682 G T 42 95 LUAD TCGA-75-5146 P2RY6 SNP Silent 11 73008274 G T 39 30 LUSC TCGA-85-6561 P2RY6 SNP Nonsense_Mutation 11 73007627 G T 37 95 BRCA TCGA-A8-A07F P2RY6 SNP Missense_Mutation 11 73008182 G T 46 73 CRC TCGA-AG-3580 P2RY6 SNP Missense_Mutation 11 73007862 G A 38 64 UCEC TCGA-AP-A051 P2RY6 SNP Silent 11 73007611 C A 21 49 UCEC TCGA-AP-A051 P2RY6 SNP Missense_Mutation 11 73008084 G A 38 95 UCEC TCGA-AP-A0LE P2RY6 SNP Missense_Mutation 11 73007750 G A 40 60 UCEC TCGA-AP-A0LM P2RY6 SNP Missense_Mutation 11 73008128 T G 53 74 UCEC TCGA-AX-A063 P2RY6 SNP Silent 11 73007797 C A 22 60 UCEC TCGA-AX-A0J0 P2RY6 SNP Missense_Mutation 11 73007730 G A 39 58 UCEC TCGA-AX-A0J1 P2RY6 SNP Missense_Mutation 11 73007645 C A 28 73 HNSC TCGA-D6-6824 P2RY6 SNP Missense_Mutation 11 73008161 G T 39 82 HNSC TCGA-DQ-7595 P2RY6 SNP Missense_Mutation 11 73008014 G A 40 74