ClinVar Miner

Submissions for variant NM_013339.4(ALG6):c.498T>G (p.Tyr166Ter)

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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 RCV003614509 SCV004400990 pathogenic ALG6-congenital disorder of glycosylation 1C 2023-12-24 criteria provided, single submitter clinical testing This sequence change creates a premature translational stop signal (p.Tyr166*) in the ALG6 gene. It is expected to result in an absent or disrupted protein product. Loss-of-function variants in ALG6 are known to be pathogenic (PMID: 19862844). This variant is not present in population databases (gnomAD no frequency). This variant has not been reported in the literature in individuals affected with ALG6-related conditions. For these reasons, this variant has been classified as Pathogenic.

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