Identifying a novel SRCAP variant in floating-harbor syndrome and prenatal genetic diagnosis in this Chinese family: A case report

Figure 2 Intron-exon structure bearing domain structure of the SRCAP gene. A: The ratio of variant types of SRCAP in the Human Gene Mutation database; B: Locations of c.7235delinsGT (p.Thr2412fs) variant found in our proband are shown. HSA, Helicase-SANT-associated domain.