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. This evidence concerns the gene CTNNB1 and neoplasm.