ttype patient gene classification type chr pos ref_allele newbase context65 cons46 CLL CW226 AP1M2 SNP Missense_Mutation 19 10692454 G T 39 97 MEL MEL-JWCI-27 AP1M2 SNP Silent 19 10692456 G A 41 55 MEL MEL-JWCI-WGS-22 AP1M2 SNP Silent 19 10685601 G A 36 55 MEL MEL-Ma-Mel-04 AP1M2 SNP Nonsense_Mutation 19 10692540 G T 36 62 OV TCGA-13-0724 AP1M2 SNP Missense_Mutation 19 10690457 G A 39 82 OV TCGA-13-1488 AP1M2 SNP Missense_Mutation 19 10689606 C G 29 95 LUAD TCGA-17-Z010 AP1M2 SNP Silent 19 10692546 G A 38 26 LUAD TCGA-17-Z014 AP1M2 SNP Nonsense_Mutation 19 10692527 C A 30 82 LUSC TCGA-18-3409 AP1M2 DEL Frame_Shift_Del 19 10685628 G - 47 47 LUAD TCGA-44-6778 AP1M2 SNP Missense_Mutation 19 10692296 T C 55 88 CRC TCGA-AA-A01P AP1M2 SNP Missense_Mutation 19 10689573 C T 18 67 UCEC TCGA-AP-A059 AP1M2 SNP Missense_Mutation 19 10692439 C T 28 84 UCEC TCGA-AX-A0J1 AP1M2 SNP Silent 19 10694699 A G 5 44 UCEC TCGA-B5-A0JZ AP1M2 SNP Missense_Mutation 19 10685603 A G 15 89 UCEC TCGA-B5-A11E AP1M2 SNP Missense_Mutation 19 10692494 C T 19 63 UCEC TCGA-B5-A11V AP1M2 SNP Silent 19 10692244 G A 40 47 UCEC TCGA-B5-A11Y AP1M2 SNP Missense_Mutation 19 10690406 G A 39 72 BRCA TCGA-BH-A1EW AP1M2 SNP Missense_Mutation 19 10690471 C A 27 95 BRCA TCGA-BH-A1F8 AP1M2 SNP Silent 19 10691955 G A 37 46 UCEC TCGA-BS-A0UF AP1M2 SNP Splice_Site 19 10690390 A C 6 87 UCEC TCGA-BS-A0UF AP1M2 SNP Missense_Mutation 19 10692225 C T 31 96 UCEC TCGA-BS-A0UM AP1M2 SNP Missense_Mutation 19 10689588 G A 39 71 BLCA TCGA-BT-A0YX AP1M2 SNP Silent 19 10692042 C T 29 54 HNSC TCGA-CN-4723 AP1M2 SNP Silent 19 10689577 G A 45 66 UCEC TCGA-D1-A103 AP1M2 SNP Splice_Site 19 10689640 C A 24 93 UCEC TCGA-E6-A1LZ AP1M2 SNP Missense_Mutation 19 10694609 G C 45 96 BRCA TCGA-E9-A228 AP1M2 SNP Missense_Mutation 19 10689625 G C 33 57 CARC Carc-H32 AP1M2 SNP Missense_Mutation 19 10687997 G C 40 53