ClinVar Miner

Submissions for variant NM_001035.3(RYR2):c.2260G>T (p.Val754Phe)

gnomAD frequency: 0.00001  dbSNP: rs376923538
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002536995 SCV000934557 uncertain significance Catecholaminergic polymorphic ventricular tachycardia 1 2023-01-28 criteria provided, single submitter clinical testing This sequence change replaces valine, which is neutral and non-polar, with phenylalanine, which is neutral and non-polar, at codon 754 of the RYR2 protein (p.Val754Phe). This variant is present in population databases (rs376923538, gnomAD 0.01%). This variant has not been reported in the literature in individuals affected with RYR2-related conditions. ClinVar contains an entry for this variant (Variation ID: 641794). Algorithms developed to predict the effect of missense changes on protein structure and function (SIFT, PolyPhen-2, Align-GVGD) all suggest that this variant is likely to be disruptive. 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.

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