ttype patient gene classification type chr pos ref_allele newbase context65 cons46 ESO ESO-085 THRA SNP Silent 17 38245559 G A 38 55 ESO ESO-105 THRA SNP Missense_Mutation 17 38243049 C G 29 66 MEL MEL-Ma-Mel-94 THRA SNP Silent 17 38243061 C T 29 62 LUAD TCGA-05-4396 THRA SNP Missense_Mutation 17 38244622 G C 39 96 LUAD TCGA-50-5930 THRA SNP Silent 17 38240228 C T 21 69 LUSC TCGA-60-2698 THRA SNP Nonsense_Mutation 17 38230776 C G 29 76 LUAD TCGA-73-4670 THRA SNP Silent 17 38245466 G C 39 50 KIRC TCGA-A3-3319 THRA INS Frame_Shift_Ins 17 38245611 - C 42 96 CRC TCGA-AA-3821 THRA SNP Missense_Mutation 17 38244642 G A 39 96 CRC TCGA-AA-A010 THRA SNP Missense_Mutation 17 38244625 A G 11 66 AML TCGA-AB-2826 THRA SNP Missense_Mutation 17 38241012 G A 42 96 UCEC TCGA-AP-A051 THRA SNP Missense_Mutation 17 38244516 A G 8 88 UCEC TCGA-AP-A059 THRA SNP Silent 17 38244584 C T 27 49 UCEC TCGA-AP-A05P THRA SNP Missense_Mutation 17 38245662 C T 20 82 UCEC TCGA-AP-A0LM THRA SNP Translation_Start_Site 17 38230594 G T 35 56 UCEC TCGA-AP-A0LM THRA SNP Missense_Mutation 17 38230786 G T 35 59 UCEC TCGA-AX-A0J1 THRA SNP Silent 17 38233855 C T 28 59 KIRC TCGA-B0-4823 THRA SNP Splice_Site 17 38243108 T A 59 88 UCEC TCGA-B5-A11E THRA SNP Missense_Mutation 17 38249402 C T 23 59 UCEC TCGA-BS-A0UF THRA SNP Missense_Mutation 17 38244633 A G 5 88 HNSC TCGA-CV-6935 THRA SNP Missense_Mutation 17 38249328 C A 23 55 HNSC TCGA-CV-7089 THRA DEL Frame_Shift_Del 17 38241015 CATCGCAG - 21 96 HNSC TCGA-CV-7252 THRA SNP Missense_Mutation 17 38245491 G C 37 81 BLCA TCGA-DK-A2I2 THRA SNP Silent 17 38244572 C T 19 54 BRCA TCGA-E2-A14V THRA SNP Missense_Mutation 17 38230773 G T 43 63 HNSC TCGA-HL-7533 THRA SNP Missense_Mutation 17 38240145 G A 45 75