ttype patient gene classification type chr pos ref_allele newbase context65 cons46 MEL ME050 TTC22 SNP Missense_Mutation 1 55252653 C T 31 69 MEL MEL-JWCI-27 TTC22 SNP Nonsense_Mutation 1 55251691 C A 32 69 MM MM-0488 TTC22 SNP Missense_Mutation 1 55252674 C T 29 90 LUAD TCGA-05-4397 TTC22 DNP Nonsense_Mutation 1 55253465 CC AA 30 75 LUAD TCGA-05-4397 TTC22 SNP Missense_Mutation 1 55253466 C A 24 63 GBM TCGA-06-0119 TTC22 SNP Silent 1 55266546 C T 23 43 LUAD TCGA-55-1592 TTC22 SNP Missense_Mutation 1 55266541 T C 60 84 LUAD TCGA-73-4668 TTC22 SNP Silent 1 55253433 C A 27 31 KIRC TCGA-A3-3320 TTC22 SNP Silent 1 55251692 T C 55 49 CRC TCGA-AA-A017 TTC22 SNP Missense_Mutation 1 55253429 C T 26 52 BRCA TCGA-AN-A0FY TTC22 SNP Missense_Mutation 1 55253434 G A 40 75 UCEC TCGA-AP-A051 TTC22 SNP Missense_Mutation 1 55251777 C T 27 67 UCEC TCGA-AP-A0LM TTC22 SNP Missense_Mutation 1 55266782 C T 30 90 UCEC TCGA-B5-A11E TTC22 SNP Missense_Mutation 1 55252683 C A 22 73 HNSC TCGA-CN-6020 TTC22 SNP Missense_Mutation 1 55266812 C T 31 87 HNSC TCGA-D6-6516 TTC22 SNP Missense_Mutation 1 55252653 C A 31 69 BRCA TCGA-D8-A27K TTC22 SNP Silent 1 55251674 C T 19 39 CARC Carc-H27 TTC22 SNP Missense_Mutation 1 55266776 G C 35 65