ClinVar Miner

Submissions for variant NM_005609.4(PYGM):c.1009C>T (p.Gln337Ter)

dbSNP: rs2135834746
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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 RCV001941724 SCV002231144 pathogenic Glycogen storage disease, type V 2020-12-18 criteria provided, single submitter clinical testing This variant has not been reported in the literature in individuals with PYGM-related conditions. This variant is not present in population databases (ExAC no frequency). This sequence change creates a premature translational stop signal (p.Gln337*) in the PYGM gene. It is expected to result in an absent or disrupted protein product. Loss-of-function variants in PYGM are known to be pathogenic (PMID: 8316268, 16786513). For these reasons, this variant has been classified as Pathogenic.

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