We confirmed all exome-seq variants in the “common” gene set in all four tumor cell lines; the presence of Tp53 mutations in the FAT7 (R271H) and NBTII lines (R211W, I230T), and its absence in the C6 and DSL-6A/C1 cell lines, missense mutations for the oncogenes Ncor1 (E544D) across all four cells lines and Pick3ca in the C6 (C90Y) and the NBTII (M811 T) cell lines. The gene discussed is NCOR1; the disease is neoplasm.