ttype patient gene classification type chr pos ref_allele newbase context65 cons46 LUAD LUAD-NYU201 HOXC13 SNP Missense_Mutation 12 54333321 G T 40 66 LUAD LUAD-S00488 HOXC13 SNP Missense_Mutation 12 54338823 G T 38 97 LUAD TCGA-05-4396 HOXC13 SNP Missense_Mutation 12 54333156 C A 26 66 LUAD TCGA-05-4410 HOXC13 SNP Missense_Mutation 12 54333267 G T 44 78 GBM TCGA-14-1825 HOXC13 SNP Missense_Mutation 12 54332758 C T 27 88 LUAD TCGA-17-Z026 HOXC13 SNP Missense_Mutation 12 54338903 A T 6 89 LUAD TCGA-64-5778 HOXC13 SNP Missense_Mutation 12 54338921 C G 27 73 LUAD TCGA-67-3771 HOXC13 SNP Missense_Mutation 12 54338891 A G 15 89 UCEC TCGA-A5-A0RA HOXC13 INS In_Frame_Ins 12 54332733 - TTA 24 64 CRC TCGA-AA-3516 HOXC13 SNP Silent 12 54339019 G A 38 52 CRC TCGA-AA-3819 HOXC13 SNP Missense_Mutation 12 54338891 A C 15 89 CRC TCGA-AA-A010 HOXC13 SNP Missense_Mutation 12 54338957 G T 44 97 CRC TCGA-AG-A002 HOXC13 SNP Missense_Mutation 12 54339018 C T 27 84 UCEC TCGA-AP-A051 HOXC13 SNP Missense_Mutation 12 54339018 C T 27 84 UCEC TCGA-AP-A056 HOXC13 SNP Missense_Mutation 12 54338822 C T 27 71 UCEC TCGA-AX-A0J1 HOXC13 SNP Missense_Mutation 12 54339018 C T 27 84 HNSC TCGA-BA-4078 HOXC13 SNP Missense_Mutation 12 54338804 G A 37 97 BLCA TCGA-CF-A3MI HOXC13 SNP Missense_Mutation 12 54339012 C T 31 75 HNSC TCGA-CN-5369 HOXC13 SNP Missense_Mutation 12 54338828 C T 27 82 HNSC TCGA-CR-6472 HOXC13 SNP Missense_Mutation 12 54338956 G C 35 50 HNSC TCGA-CV-7414 HOXC13 SNP Missense_Mutation 12 54332775 G A 39 54