ClinVar

Description

The R179H variant in the KRT5 gene has not been reported previously as a pathogenic variant, nor as a benign variant, to our knowledge. It was observed at low frequency in approximately 6,500 individuals of European and African American ancestry by the NHLBI Exome Sequencing Project and also in a GeneDx cohort of controls. This substitution occurs within a known mutational hotspot region (helix initiation motif) that is highly conserved across all species and among all members of the keratin family. Many other pathogenic variants in patients with epidermolysis bullosa simplex have been reported in nearby residues (E178K, Q181P I182N) according to the Human Gene Mutation Database (Stenson et al., 2014). However, this missense change occurs at a nucleotide position that is not conserved and in silico analysis is inconsistent in its predictions as to whether or not the variant is damaging to the protein structure/function. Therefore, we interpret R179H as a variant of uncertain significance.