ClinVar

Description

The c.99 G>A variant of uncertain significance in the TMEM43 gene has not been published as pathogenic or been reported as benign to our knowledge. This variant is not observed at a significant frequency in large population cohorts (Lek et al., 2016; 1000 Genomes Consortium et al., 2015; Exome Variant Server). Although c.99 G>A results in a synonymous amino acid substitution (S33S), in silico splice prediction programs predict this variant may create a cryptic splice donor site upstream from the natural splice donor site, and may cause abnormal gene splicing. However, in the absence of functional mRNA studies, the physiological consequence of this variant cannot be precisely determined. Furthermore, this substitution occurs at a nucleotide that is not conserved across species, and adenine (A) is the wild-type nucleotide at this position in some species. Finally, no pathogenic splice site variants in the TMEM43 gene have been reported in the Human Gene Mutation Database (Stenson et al., 2014).