Whole-Exome Sequencing Identifies One De Novo Variant in the FGD6 Gene in a Thai Family with Autism Spectrum Disorder

Figure 3

Chromatograms of 2 heterozygous missense variants in EIF2AK3 (a), FGD6 (b), and CHD8 (c) gene. Letters in [] indicate complementary (FWD) alleles.

(a) EIF2AK3 c.2014G>A [C>T]

(b) FGD6 c.2951G>A [C>T]

(c) CHD8 c.6119A>G [T>C]