ClinVar

Description

The alteration results in an amino acid change:_x000D_ _x000D_ The c.230G>A (p.G77D) alteration is located in exon 6 (coding exon 4) of the GNB1 gene. This alteration results from a G to A substitution at nucleotide position 230, causing the glycine (G) at amino acid position 77 to be replaced by an aspartic acid (D). The alteration is not observed in population databases: _x000D_ _x000D_ Based on data from the Genome Aggregation Database (gnomAD), the GNB1 c.230G>A alteration was not observed, with coverage at this position. Alterations at the same codon has been observed in affected individuals:_x000D_ _x000D_ Several alterations have been described at the same codon to occur de novo in patients with a neurodevelopmental phenotype, including p.G77S, p.G77V, p.G77R, and p.G77A. All patients present with global developmental delay and hypotonia, while additional features have been reported in some including congenital defects, dystonia, eye abnormalities, acute lymphoblastic leukemia, and cutaneous mastocystosis (Brett, 2017; Hemati, 2018; Petrovski, 2016; Szcaluba, 2018). Additionally, de novo changes in neighboring amino acid residues (p.D76 and p.K78) have been reported in three additional individuals with global developmental delay, hypotonia, and epilepsy (Petrovski, 2016). The altered amino acid is conserved throughout evolution:_x000D_ _x000D_ The p.G77 amino acid is conserved in available vertebrate species. The amino acid is located in a functionally important protein domain:_x000D_ _x000D_ The p.G77 amino acid is located in a WD40 repeat region in the amino-terminal interface of GNB1. Crystal structures of heterotrimeric G-alpha-beta-gamma have demonstrated that this is a region of interaction between the G-protein beta subunit and alpha subunit (Ford, 1998). The adjacent p.K78 residue is reported to play an important role in regulating activation of adenylyl cyclase 2, inhibition of calcium channels, and activation of potassium channels (Ford, 1998; Petrovski, 2016). The alteration is predicted deleterious by in silico models:_x000D_ _x000D_ The p.G77D alteration is predicted to be probably damaging by Polyphen and deleterious by SIFT in silico analyses. Based on the available evidence, this alteration is classified as likely pathogenic.