Total submissions: 1
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Labcorp Genetics |
RCV003856060 | SCV004656274 | uncertain significance | 2-aminoadipic 2-oxoadipic aciduria | 2023-11-11 | criteria provided, single submitter | clinical testing | This sequence change replaces histidine, which is basic and polar, with tyrosine, which is neutral and polar, at codon 859 of the DHTKD1 protein (p.His859Tyr). This variant is present in population databases (rs769419156, gnomAD 0.0009%). This variant has not been reported in the literature in individuals affected with DHTKD1-related conditions. An algorithm developed to predict the effect of missense changes on protein structure and function (PolyPhen-2) suggests that this variant is likely to be tolerated. 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. |