ClinVar Miner

Submissions for variant NM_182961.4(SYNE1):c.11609A>G (p.Glu3870Gly)

gnomAD frequency: 0.00002  dbSNP: rs771572017
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Eurofins Ntd Llc (ga) RCV000401974 SCV000342371 uncertain significance not provided 2016-06-22 criteria provided, single submitter clinical testing
Invitae RCV002518031 SCV003284861 uncertain significance Autosomal recessive ataxia, Beauce type; Emery-Dreifuss muscular dystrophy 4, autosomal dominant 2022-10-17 criteria provided, single submitter clinical testing This sequence change replaces glutamic acid, which is acidic and polar, with glycine, which is neutral and non-polar, at codon 3855 of the SYNE1 protein (p.Glu3855Gly). This variant is present in population databases (rs771572017, gnomAD 0.01%). This variant has not been reported in the literature in individuals affected with SYNE1-related conditions. ClinVar contains an entry for this variant (Variation ID: 288299). 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 disruptive. 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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