ClinVar

Description

The homozygous c.1503-2A>G variant in GAN was identified by our study in one individual with global developmental delay and neurodegeneration. The c.1503-2A>G variant in GAN has not been previously reported in individuals with giant axonal neuropathy 1. This variant was absent from the large population studies. This variant is located in the 5' splice region. Computational tools predict a splicing impact, though this information is not predictive enough to determine pathogenicity. There is an in-frame cryptic splice site 108 bases from the intron-exon boundary, providing evidence that this variant may delete 36 amino acids instead of causing loss of function. However, this information is not predictive enough to determine pathogenicity. Loss of function of the GAN gene is an established disease mechanism in autosomal recessive giant axonal neuropathy 1. In summary, while there is some suspicion for a pathogenic role, the clinical significance of this variant is uncertain. ACMG/AMP Criteria applied: PVS1_Moderate, PM2_Supporting, PM3_Supporting (Richards 2015).