Total submissions: 1
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Invitae | RCV002233144 | SCV000814464 | pathogenic | Ectodermal dysplasia 10A, hypohidrotic/hair/nail type, autosomal dominant; Autosomal recessive hypohidrotic ectodermal dysplasia syndrome | 2018-05-23 | criteria provided, single submitter | clinical testing | This sequence change results in a premature translational stop signal in the EDAR gene (p.Tyr364Thrfs*8). While this is not anticipated to result in nonsense mediated decay, it is expected to disrupt the last 85 amino acids of the EDAR protein. This variant is not present in population databases (ExAC no frequency). This variant has not been reported in the literature in individuals with EDAR-related disease. A different truncation (p.Phe398*) that lies downstream of this variant has been reported in families with ectodermal dysplasia and determined to be pathogenic (PMID: 23401279, 24641098). This suggests that deletion of this region of the EDAR protein is causative of disease. For these reasons, this variant has been classified as Pathogenic. |