ClinVar Miner

Submissions for variant NM_000540.3(RYR1):c.6953del (p.Tyr2318fs)

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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 RCV005120088 SCV005739222 pathogenic RYR1-related disorder 2024-02-03 criteria provided, single submitter clinical testing This sequence change creates a premature translational stop signal (p.Tyr2318Serfs*112) in the RYR1 gene. It is expected to result in an absent or disrupted protein product. Loss-of-function variants in RYR1 are known to be pathogenic (PMID: 23919265, 25960145, 28818389, 30611313). This variant is not present in population databases (gnomAD no frequency). This variant has not been reported in the literature in individuals affected with RYR1-related conditions. For these reasons, this variant has been classified as Pathogenic.

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