In addition, the most common changes in CNV were FGF3, TERT, and SOX2, and their variant rates were all higher than those reported in cBioPortal-HCC patients (15.4% vs. 5.0%; 12.8% vs. 4.0%; 12.8% vs. 1.1%, respectively). The gene discussed is FGF3; the disease is hepatocellular carcinoma.