ttype patient gene classification type chr pos ref_allele newbase context65 cons46 ESO ESO-0015 ACP2 SNP Splice_site 11 47267025 T C 55 47 LUAD LUAD-GU4I3 ACP2 SNP Silent 11 47266326 G A 37 54 LUAD LUAD-YINHD ACP2 SNP Silent 11 47264867 G A 35 57 OV TCGA-13-0884 ACP2 SNP Missense_Mutation 11 47266885 A G 7 87 LUAD TCGA-17-Z032 ACP2 SNP Missense_Mutation 11 47264815 A G 11 60 LUAD TCGA-44-2665 ACP2 INS Splice_Site 11 47266284 - C 6 85 LUAD TCGA-50-6597 ACP2 SNP Nonsense_Mutation 11 47261720 G A 46 65 LUSC TCGA-66-2768 ACP2 SNP Missense_Mutation 11 47267352 G C 33 76 CRC TCGA-AA-3672 ACP2 SNP Missense_Mutation 11 47264423 C T 23 96 CRC TCGA-AA-A00J ACP2 SNP Missense_Mutation 11 47267093 G A 39 82 CRC TCGA-AG-3892 ACP2 SNP Silent 11 47267287 C T 31 40 UCEC TCGA-AP-A056 ACP2 SNP Missense_Mutation 11 47267035 G A 33 46 UCEC TCGA-AP-A0LM ACP2 SNP Silent 11 47266892 C T 32 60 UCEC TCGA-B5-A11J ACP2 SNP Nonsense_Mutation 11 47264310 G A 46 63 KIRC TCGA-CZ-5453 ACP2 SNP Missense_Mutation 11 47267291 T A 60 69 HNSC TCGA-DQ-5625 ACP2 SNP Missense_Mutation 11 47261735 C T 19 57