The KIT mutations were located in the activation loop of the KIT protein tyrosine kinase 2 (n = 19), the juxtamembrane domain (n = 6), and the protein tyrosine kinase 1 domain (n = 1), resembling those previously described in TGCTs (Litchfield et al., 2015) and intracranial germ cell tumors (Wang et al., 2014) (Figure S2D). The gene discussed is PTK2; the disease is testicular germ cell tumor.