ttype patient gene classification type chr pos ref_allele newbase context65 cons46 ESO ESO-251 GHITM SNP Missense_Mutation 10 85901287 A G 10 60 LUAD LUAD-F00170 GHITM SNP Missense_Mutation 10 85909822 G A 46 73 LUAD LUAD-RT-S01810 GHITM SNP Missense_Mutation 10 85903810 T C 59 76 LUAD TCGA-17-Z014 GHITM SNP Silent 10 85901331 C T 22 50 LUSC TCGA-63-5131 GHITM SNP Missense_Mutation 10 85901279 G T 48 91 LUSC TCGA-66-2785 GHITM SNP Missense_Mutation 10 85904678 A T 14 90 LUAD TCGA-75-6211 GHITM SNP Silent 10 85904649 C G 29 68 UCEC TCGA-A5-A0GP GHITM SNP Missense_Mutation 10 85909925 C T 27 81 CRC TCGA-AA-3846 GHITM SNP Silent 10 85903785 G A 43 49 CRC TCGA-AA-A01S GHITM SNP Missense_Mutation 10 85912074 G A 46 54 CRC TCGA-AG-A002 GHITM SNP Nonsense_Mutation 10 85903852 G T 45 98 UCEC TCGA-AP-A051 GHITM SNP Missense_Mutation 10 85901354 C T 19 51 UCEC TCGA-AP-A056 GHITM SNP Nonsense_Mutation 10 85903762 G T 43 98 UCEC TCGA-AP-A059 GHITM SNP Missense_Mutation 10 85903790 C T 28 62 UCEC TCGA-AP-A0LM GHITM SNP Missense_Mutation 10 85909991 C T 30 94 UCEC TCGA-AX-A0J0 GHITM SNP Missense_Mutation 10 85904701 A G 2 90 UCEC TCGA-AX-A0J1 GHITM SNP Nonsense_Mutation 10 85904637 G A 42 98 UCEC TCGA-B5-A11X GHITM SNP Missense_Mutation 10 85909925 C T 27 81 BRCA TCGA-BH-A0DL GHITM SNP Missense_Mutation 10 85902493 T C 51 57 BLCA TCGA-BT-A3PJ GHITM SNP Missense_Mutation 10 85903844 G A 41 84 HNSC TCGA-CV-5441 GHITM SNP Silent 10 85901368 C T 28 70 HNSC TCGA-CV-6003 GHITM SNP Missense_Mutation 10 85903817 A G 16 89 BRCA TCGA-E2-A15S GHITM SNP Silent 10 85901316 T G 56 45