Skip to main content
Figure 1 | Molecular Autism

Figure 1

From: Genetic analysis of GABRB3 as a candidate gene of autism spectrum disorders

Figure 1

Schematic genomic structure of the GABRB3 gene and the locations of genetic variants identified in this study. The black boxes represent the protein-coding regions, while the open boxes represent the untranslated regions. SNPs identified in this study are listed below the schematic genomic structure and displayed in purple text. The positions of SNPs in the exon 1a promoter are numbered from the ATG start site. With regard to rare mutations, patient-specific mutations are displayed in red text, those discovered in controls only are displayed in green text, and those identified both in patients and controls are displayed in black text. IVS: intervening sequence; F: phenylalanine, T: threonine, S: serine, M: methionine, Y: tyrosine, H; histidine; del: deletion; ins: insertion.

Back to article page