ttype patient gene classification type chr pos ref_allele newbase context65 cons46 BRCA BR-0054 TALDO1 SNP Missense_Mutation 11 764389 C T 23 71 PRAD P04-1421 TALDO1 SNP Missense_Mutation 11 763815 G A 38 93 LUAD TCGA-05-4410 TALDO1 SNP Missense_Mutation 11 764307 A G 1 73 LUSC TCGA-39-5039 TALDO1 SNP Missense_Mutation 11 755975 C A 27 72 LUSC TCGA-46-3769 TALDO1 SNP Missense_Mutation 11 764383 G T 39 94 LUAD TCGA-73-4662 TALDO1 SNP Silent 11 763398 C T 31 51 UCEC TCGA-A5-A0GI TALDO1 SNP Missense_Mutation 11 763825 G A 38 80 CRC TCGA-A6-2676 TALDO1 SNP Silent 11 760170 C T 31 38 CRC TCGA-AA-3516 TALDO1 SNP Missense_Mutation 11 755917 C A 22 94 CRC TCGA-AA-3819 TALDO1 SNP Silent 11 763910 C T 19 61 CRC TCGA-AA-A010 TALDO1 SNP Missense_Mutation 11 764308 A C 1 73 CRC TCGA-AA-A01Q TALDO1 SNP Missense_Mutation 11 759053 G A 38 76 UCEC TCGA-AP-A051 TALDO1 SNP Missense_Mutation 11 759053 G A 38 76 UCEC TCGA-AP-A056 TALDO1 SNP Missense_Mutation 11 755887 G A 37 80 UCEC TCGA-AP-A056 TALDO1 SNP Missense_Mutation 11 764325 G T 33 67 UCEC TCGA-AP-A056 TALDO1 SNP Missense_Mutation 11 764833 G T 33 53 UCEC TCGA-AX-A05Z TALDO1 SNP Missense_Mutation 11 763784 G T 33 58 UCEC TCGA-AX-A05Z TALDO1 SNP Missense_Mutation 11 763789 T G 64 73 UCEC TCGA-AX-A0J1 TALDO1 SNP Missense_Mutation 11 759053 G A 38 76 KIRC TCGA-B0-4822 TALDO1 SNP Missense_Mutation 11 755932 G T 42 94 KIRC TCGA-BP-4999 TALDO1 SNP Silent 11 747520 C T 23 51 BLCA TCGA-BT-A2LB TALDO1 SNP Silent 11 763392 C T 32 80 HNSC TCGA-CR-6472 TALDO1 SNP Silent 11 747535 C G 29 57 HNSC TCGA-CV-6950 TALDO1 SNP Silent 11 755976 G A 37 52 KIRC TCGA-CZ-5459 TALDO1 SNP Missense_Mutation 11 763505 C A 22 93