ClinVar Miner

Submissions for variant NM_015599.3(PGM3):c.1198_1202dup (p.Ala402fs)

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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 RCV003874778 SCV004683362 pathogenic Immunodeficiency 23 2024-01-21 criteria provided, single submitter clinical testing This sequence change creates a premature translational stop signal (p.Ala430Lysfs*26) in the PGM3 gene. It is expected to result in an absent or disrupted protein product. Loss-of-function variants in PGM3 are known to be pathogenic (PMID: 17548465, 24589341, 24931394). This variant is present in population databases (no rsID available, gnomAD 0.003%). This variant has not been reported in the literature in individuals affected with PGM3-related conditions. For these reasons, this variant has been classified as Pathogenic.

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