ClinVar Miner

Submissions for variant NM_002863.5(PYGL):c.1286T>A (p.Met429Lys)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Neuberg Centre For Genomic Medicine, NCGM RCV003340782 SCV004047500 uncertain significance Glycogen storage disease, type VI criteria provided, single submitter clinical testing The missense variant in c.1286T>A in PYGL gene has not been reported previously as a pathogenic variant nor as a benign variant, to our knowledge. The p.Met429Lys variant is novel (not in any individuals) in gnomAD Exomes and 1000 Genomes. This variant has not been reported to the ClinVar database. The amino acid change p.Met429Lys in PYGL is predicted as conserved by GERP++ and PhyloP across 100 vertebrates. The amino acid Met at position 429 is changed to a Lys changing protein sequence and it might alter its composition and physico-chemical properties. For these reasons, this variant has been classified as Uncertain Significance (VUS).

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