ClinVar Miner

Submissions for variant NM_182961.4(SYNE1):c.11309A>G (p.Lys3770Arg)

gnomAD frequency: 0.00004  dbSNP: rs780693119
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Eurofins Ntd Llc (ga) RCV000734523 SCV000862673 uncertain significance not provided 2018-07-31 criteria provided, single submitter clinical testing
Invitae RCV000821714 SCV000962483 uncertain significance Autosomal recessive ataxia, Beauce type; Emery-Dreifuss muscular dystrophy 4, autosomal dominant 2022-07-05 criteria provided, single submitter clinical testing This sequence change replaces lysine, which is basic and polar, with arginine, which is basic and polar, at codon 3755 of the SYNE1 protein (p.Lys3755Arg). This variant is present in population databases (rs780693119, gnomAD 0.005%). 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: 598188). 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 C25"). 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.
Athena Diagnostics Inc RCV000734523 SCV001880801 uncertain significance not provided 2020-11-06 criteria provided, single submitter clinical testing

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