Total submissions: 1
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Labcorp Genetics |
RCV003529054 | SCV004270268 | uncertain significance | 2-aminoadipic 2-oxoadipic aciduria | 2023-05-12 | criteria provided, single submitter | clinical testing | This variant has not been reported in the literature in individuals affected with DHTKD1-related conditions. This variant is present in population databases (rs766464907, gnomAD 0.002%). This sequence change replaces tryptophan, which is neutral and slightly polar, with arginine, which is basic and polar, at codon 571 of the DHTKD1 protein (p.Trp571Arg). In summary, the available evidence is currently insufficient to determine the role of this variant in disease. Therefore, it has been classified as a Variant of Uncertain Significance. Advanced modeling of protein sequence and biophysical properties (such as structural, functional, and spatial information, amino acid conservation, physicochemical variation, residue mobility, and thermodynamic stability) performed at Invitae indicates that this missense variant is expected to disrupt DHTKD1 protein function. |