ClinVar Miner

Submissions for variant NM_001035.3(RYR2):c.2482C>T (p.Pro828Ser) (rs794728698)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV000182623 SCV000234989 uncertain significance not provided 2016-09-22 criteria provided, single submitter clinical testing The P828S variant in the RYR2 gene has not been reported as a pathogenic variant or a benign variant, to our knowledge. The P828S variant was not observed in approximately 6,100 individuals of European and African American ancestry in the NHLBI Exome Sequencing Project, indicating it is not a common benign variant in these populations. P828S results in a non-conservative amino acid substitution of non-polar Proline with a neutral, polar Serine at a position that is conserved across species. Consequently, in silico analysis predicts this variant is probably damaging to the protein structure/function. However, the P828S variant is not located in one of the three hot-spot regions of the RYR2 gene, where the majority of pathogenic missense variants occur and no pathogenic variants have been reported in nearby residues to date (Medeiros-Domingo A et al., 2009; Stenson P et al., 2014).

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