ttype patient gene classification type chr pos ref_allele newbase context65 cons46 ESO ESO-2143 CHST12 SNP Missense_Mutation 7 2472473 G A 37 66 LUAD LUAD-F00368 CHST12 SNP Missense_Mutation 7 2473077 G T 38 58 MEL ME017 CHST12 SNP Silent 7 2473507 C T 30 46 MEL ME049 CHST12 SNP Missense_Mutation 7 2472407 A C 6 42 MEL MEL-JWCI-WGS-1 CHST12 SNP Silent 7 2473084 C T 31 53 MEL MEL-JWCI-WGS-13 CHST12 SNP Silent 7 2472997 C T 30 63 MEL MEL-JWCI-WGS-24 CHST12 SNP Missense_Mutation 7 2472881 C T 22 100 MEL MEL-Ma-Mel-48 CHST12 SNP Missense_Mutation 7 2472587 G A 37 71 MEL MEL-UKRV-Mel-20 CHST12 DNP Missense_Mutation 7 2472723 CC TT 22 99 MM MM-0531 CHST12 SNP Silent 7 2473108 C T 19 59 MM MM-0597 CHST12 SNP Missense_Mutation 7 2472650 A T 11 56 MEL Mel_BRAFi_02_PRE CHST12 SNP Silent 7 2472997 C T 30 63 LUAD TCGA-05-4382 CHST12 SNP Missense_Mutation 7 2472659 C T 27 50 LUSC TCGA-39-5039 CHST12 SNP Missense_Mutation 7 2472891 A G 6 54 LUAD TCGA-44-6779 CHST12 SNP Missense_Mutation 7 2473023 G A 38 100 LUSC TCGA-60-2698 CHST12 SNP Silent 7 2472883 G A 38 42 LUAD TCGA-64-5779 CHST12 SNP Missense_Mutation 7 2473357 G T 34 44 BRCA TCGA-A8-A09Q CHST12 SNP Silent 7 2473288 C T 31 48 CRC TCGA-AA-3672 CHST12 SNP Missense_Mutation 7 2473211 G A 41 100 CRC TCGA-AA-3864 CHST12 SNP Missense_Mutation 7 2472318 C T 31 85 CRC TCGA-AA-A02J CHST12 SNP Silent 7 2472883 G A 38 42 CRC TCGA-AG-3726 CHST12 SNP Missense_Mutation 7 2473376 T C 53 63 CRC TCGA-AG-A002 CHST12 SNP Silent 7 2473318 C T 19 48 CRC TCGA-AG-A01L CHST12 SNP Silent 7 2472319 G A 39 34 BRCA TCGA-AO-A0JD CHST12 SNP Silent 7 2473033 C T 23 32 UCEC TCGA-AP-A059 CHST12 SNP Missense_Mutation 7 2473508 C A 24 79 KIRC TCGA-B0-5713 CHST12 DEL Frame_Shift_Del 7 2473500 A - 9 78 UCEC TCGA-B5-A0JY CHST12 SNP Missense_Mutation 7 2472713 G A 37 99 UCEC TCGA-B5-A11E CHST12 SNP Missense_Mutation 7 2473386 G T 35 85 UCEC TCGA-BS-A0UF CHST12 SNP Silent 7 2472952 C T 32 59 BLCA TCGA-CF-A1HS CHST12 SNP Silent 7 2472655 G C 46 51 HNSC TCGA-CV-6954 CHST12 SNP Missense_Mutation 7 2472365 G A 38 57 UCEC TCGA-D1-A16F CHST12 SNP Missense_Mutation 7 2472855 C T 27 50 UCEC TCGA-D1-A17A CHST12 SNP Silent 7 2472865 C T 27 46