ClinVar Miner

Submissions for variant NM_080916.3(DGUOK):c.746del (p.Val249fs)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV005073757 SCV005706079 pathogenic not provided 2024-09-09 criteria provided, single submitter clinical testing This sequence change creates a premature translational stop signal (p.Val249Glyfs*12) in the DGUOK gene. While this is not anticipated to result in nonsense mediated decay, it is expected to disrupt the last 29 amino acid(s) of the DGUOK protein. This variant is present in population databases (no rsID available, gnomAD 0.002%). This variant has not been reported in the literature in individuals affected with DGUOK-related conditions. This variant disrupts a region of the DGUOK protein in which other variant(s) (p.Leu266Arg) have been determined to be pathogenic (PMID: 16263314, 17073823). This suggests that this is a clinically significant region of the protein, and that variants that disrupt it are likely to be disease-causing. For these reasons, this variant has been classified as Pathogenic.

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