ClinVar Miner

Submissions for variant NM_024422.6(DSC2):c.1095A>T (p.Glu365Asp)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV003632527 SCV004516930 uncertain significance Arrhythmogenic right ventricular dysplasia 11 2023-11-06 criteria provided, single submitter clinical testing This sequence change replaces glutamic acid, which is acidic and polar, with aspartic acid, which is acidic and polar, at codon 365 of the DSC2 protein (p.Glu365Asp). This variant is present in population databases (rs763335007, gnomAD 0.006%). This variant has not been reported in the literature in individuals affected with DSC2-related conditions. Advanced modeling of protein sequence and biophysical properties (such as structural, functional, and spatial information, amino acid conservation, physicochemical variation, residue mobility, and thermodynamic stability) has been performed at Invitae for this missense variant, however the output from this modeling did not meet the statistical confidence thresholds required to predict the impact of this variant on DSC2 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.
All of Us Research Program, National Institutes of Health RCV004005820 SCV004835358 uncertain significance Familial isolated arrhythmogenic right ventricular dysplasia 2023-11-30 criteria provided, single submitter clinical testing

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