ClinVar Miner

Submissions for variant NM_000540.2(RYR1):c.13909A>G (p.Thr4637Ala) (rs118192166)

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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV000119487 SCV000491288 likely pathogenic not provided 2019-01-11 criteria provided, single submitter clinical testing The T4637A variant in the RYR1 gene has been reported previously in the heterozygous state in affected individuals of a family with congenital myopathy that showed clinical and histologic features of central core disease and nemaline myopathy (Scacheri et al., 2000). The T4637A variant was not observed in approximately 6,500 individuals of European and African American ancestry in the NHLBI Exome Sequencing Project, indicating it is not a common benign variant in these populations. The T4637A variant is a non-conservative amino acid substitution, which is likely to impact secondary protein structure as these residues differ in polarity, charge, size and/or other properties. This substitution occurs at a position that is conserved across species. In silico analysis is inconsistent in its predictions as to whether or not the variant is damaging to the protein structure/function. Missense variants in the same and nearby residues (E4634K, E4635Q, T4637I, G4638S, G4638D) have been reported in the Human Gene Mutation Database in association with RYR1-related disorders (Stenson et al., 2014), supporting the functional importance of this region of the protein. The T4637A variant is a strong candidate for a pathogenic variant, however the possibility it may be a rare benign variant cannot be excluded.
Leiden Muscular Dystrophy (RYR1) RCV000119487 SCV000154394 not provided not provided no assertion provided not provided
OMIM RCV000013864 SCV000034111 pathogenic Myopathy, Central Core 2000-12-12 no assertion criteria provided literature only
PreventionGenetics RCV000119487 SCV000852375 pathogenic not provided 2016-03-09 criteria provided, single submitter clinical testing

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