ClinVar Miner

Submissions for variant NM_182961.4(SYNE1):c.862G>A (p.Ala288Thr)

gnomAD frequency: 0.00004  dbSNP: rs770907182
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Eurofins Ntd Llc (ga) RCV000173909 SCV000225085 uncertain significance not provided 2015-05-21 criteria provided, single submitter clinical testing
Invitae RCV000694792 SCV000823252 uncertain significance Autosomal recessive ataxia, Beauce type; Emery-Dreifuss muscular dystrophy 4, autosomal dominant 2022-02-25 criteria provided, single submitter clinical testing This sequence change replaces alanine, which is neutral and non-polar, with threonine, which is neutral and polar, at codon 295 of the SYNE1 protein (p.Ala295Thr). This variant is present in population databases (rs770907182, gnomAD 0.006%). 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: 193750). Algorithms developed to predict the effect of missense changes on protein structure and function output the following: SIFT: "Tolerated"; PolyPhen-2: "Benign"; Align-GVGD: "Class C0". The threonine amino acid residue is found in multiple mammalian species, which suggests that this missense change does not adversely affect protein function. 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.
CeGaT Center for Human Genetics Tuebingen RCV000173909 SCV001250182 uncertain significance not provided 2019-07-01 criteria provided, single submitter clinical testing
Athena Diagnostics Inc RCV000173909 SCV002771422 uncertain significance not provided 2022-03-11 criteria provided, single submitter clinical testing

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