ClinVar Miner

Submissions for variant NM_002103.5(GYS1):c.1007A>G (p.Asn336Ser)

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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 RCV002651104 SCV003515815 uncertain significance Glycogen storage disease due to muscle and heart glycogen synthase deficiency 2022-03-01 criteria provided, single submitter clinical testing This sequence change replaces asparagine, which is neutral and polar, with serine, which is neutral and polar, at codon 336 of the GYS1 protein (p.Asn336Ser). This variant is present in population databases (rs760811109, gnomAD 0.01%). This variant has not been reported in the literature in individuals affected with GYS1-related conditions. Algorithms developed to predict the effect of missense changes on protein structure and function are either unavailable or do not agree on the potential impact of this missense change (SIFT: "Deleterious"; PolyPhen-2: "Benign"; Align-GVGD: "Class C0"). In summary, the available evidence is currently insufficient to determine the role of this variant in disease. Therefore, it has been classified as a Variant of Uncertain Significance.

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