TERT and neoplasm: Table 2 presents details of the mutations considered to be pathogenic/likely pathogenic in the set of 10 tumors studied by exome sequencing: six LoF variants (five nonsense, and one frameshift, five of them in a single tumor), and six missense variants (recurrent variants or recurrent genes in different tumors), mutations in the promoter of TERT and intragenic CTNNB1 deletions.