ClinVar Miner

Submissions for variant NM_000540.3(RYR1):c.14590_14592del (p.Tyr4864del)

dbSNP: rs1974150661
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV001220897 SCV001392910 uncertain significance RYR1-Related Disorders 2019-07-23 criteria provided, single submitter clinical testing 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. Experimental studies and prediction algorithms are not available or were not evaluated for this variant, and the functional significance of the affected amino acid(s) is currently unknown. This variant has not been reported in the literature in individuals with RYR1-related conditions. This variant is not present in population databases (ExAC no frequency). This variant, c.14590_14592del, results in the deletion of 1 amino acid(s) of the RYR1 protein (p.Tyr4864del), but otherwise preserves the integrity of the reading frame.

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