ClinVar Miner

Submissions for variant NM_024422.6(DSC2):c.2597C>T (p.Ala866Val)

dbSNP: rs760363798
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Color Diagnostics, LLC DBA Color Health RCV001185450 SCV001351649 uncertain significance Cardiomyopathy 2020-02-05 criteria provided, single submitter clinical testing This missense variant replaces alanine with valine at codon 866 of the DSC2 protein. Computational prediction is inconclusive regarding the impact of this variant on protein structure and function (internally defined REVEL score threshold 0.5 < inconclusive < 0.7, PMID: 27666373). Splice site prediction tools suggest that this variant may not impact RNA splicing. To our knowledge, functional studies have not been performed for this variant. This variant has not been reported in individuals affected with cardiovascular disorders in the literature. This variant has been identified in 1/251152 chromosomes in the general population by the Genome Aggregation Database (gnomAD). The available evidence is insufficient to determine the role of this variant in disease conclusively. Therefore, this variant is classified as a Variant of Uncertain Significance.
Invitae RCV001859109 SCV002206827 uncertain significance Arrhythmogenic right ventricular dysplasia 11 2021-12-17 criteria provided, single submitter clinical testing This sequence change replaces alanine, which is neutral and non-polar, with valine, which is neutral and non-polar, at codon 866 of the DSC2 protein (p.Ala866Val). 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. 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: "Probably Damaging"; Align-GVGD: "Class C0"). ClinVar contains an entry for this variant (Variation ID: 924245). This variant has not been reported in the literature in individuals affected with DSC2-related conditions. This variant is not present in population databases (gnomAD no frequency).
Revvity Omics, Revvity RCV001859109 SCV003829122 uncertain significance Arrhythmogenic right ventricular dysplasia 11 2021-12-09 criteria provided, single submitter clinical testing

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