Description
The S3G variant in the SHOC2 gene has not been reported previously as a pathogenic variant, nor as a benign variant, to our knowledge. The S3G variant was not observed in approximately 6500 individuals of European and African American ancestry in the NHLBI Exome Sequencing Project, indicating it is not a common benign variant in these populations. The S3G variant is a non-conservative amino acid substitution, which is likely to impact secondary protein structure as these residues differ in polarity, charge, size and/or other properties. This substitution occurs at a position where amino acids with similar properties to Serine are tolerated across species. However, in silico analysis is inconsistent in its predictions as to whether or not the variant is damaging to the protein structure/function. The S2G neighboring missense variant has been reported in the Human Gene Mutation Database as a recurrent pathogenic variant in association with Noonan-like syndrome with loose anagen hair (Stenson et al., 2014), supporting the functional importance of this region of the protein. We interpret S3G as a variant of uncertain significance.
| # | Sample | Method | Observation |
|---|
| Origin | Affected | Number tested | Tissue | Purpose | Method | Individuals | Allele frequency | Families | Co-occurrences |
|---|
| 1 | germline | yes | not provided | not provided | not provided | | not provided | not provided | not provided | not provided |
