These included clinical and histological features (patient age, tumor size, ciliary body involvement, extraocular extension, and so on), the genetic mutations [G protein subunit alpha q (GNAQ), G protein subunit alpha 11 (GNA11), Splicing Factor 3b Subunit 1(SF3B1), BRCA1 associated protein 1(BAP1), and Eukaryotic Translation Initiation Factor 1A X-Linked (EIF1AX)], and the composition of chromosomal anomalies of chromosome 3, 6 and 8 [8]. The gene discussed is GNAQ; the disease is neoplasm.