ttype patient gene classification type chr pos ref_allele newbase context65 cons46 ESO ESO-250 TOLLIP SNP Missense_Mutation 11 1298411 C T 27 54 HNSC HN_62426 TOLLIP SNP Synonymous 11 1311553 C T 23 22 MEL MEL-JWCI-WGS-8 TOLLIP SNP Missense_Mutation 11 1298297 G A 41 94 LUSC TCGA-18-3406 TOLLIP SNP Missense_Mutation 11 1311618 C T 23 98 LUAD TCGA-44-2668 TOLLIP SNP Missense_Mutation 11 1298459 C T 26 80 LUAD TCGA-44-3918 TOLLIP SNP Missense_Mutation 11 1298328 G T 47 94 LUAD TCGA-91-6831 TOLLIP SNP Silent 11 1316878 T C 57 49 UCEC TCGA-A5-A0VP TOLLIP SNP Silent 11 1309893 G A 40 39 CRC TCGA-AA-A00J TOLLIP SNP Missense_Mutation 11 1307253 C T 19 66 UCEC TCGA-AP-A059 TOLLIP SNP Missense_Mutation 11 1309949 G T 35 81 UCEC TCGA-AP-A0LM TOLLIP SNP Missense_Mutation 11 1311482 G T 33 85 HNSC TCGA-CQ-5323 TOLLIP SNP Silent 11 1309866 G A 45 52 UCEC TCGA-D1-A103 TOLLIP SNP Silent 11 1311514 G T 45 51 BLCA TCGA-DK-A2I4 TOLLIP SNP Missense_Mutation 11 1298324 C T 31 60