ClinVar Miner

Submissions for variant NM_000337.6(SGCD):c.835G>A (p.Gly279Arg)

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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 RCV002633649 SCV003515751 uncertain significance Autosomal recessive limb-girdle muscular dystrophy type 2F 2022-08-19 criteria provided, single submitter clinical testing This sequence change replaces glycine, which is neutral and non-polar, with arginine, which is basic and polar, at codon 279 of the SGCD protein (p.Gly279Arg). This variant is present in population databases (rs778210302, gnomAD 0.0009%). This variant has not been reported in the literature in individuals affected with SGCD-related conditions. Algorithms developed to predict the effect of missense changes on protein structure and function (SIFT, PolyPhen-2, Align-GVGD) all suggest that this variant is likely to be tolerated. 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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