ClinVar Miner

Submissions for variant NM_000257.4(MYH7):c.1148A>G (p.Lys383Arg) (rs397516092)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV000480078 SCV000565284 likely pathogenic not provided 2015-02-10 criteria provided, single submitter clinical testing A likely pathogenic variant was identified in the MYH7 gene. The K383R variant has been reported as a variant of unknown significance associated with apical HCM (Gruner C et al., 2011). The K383R variant was not observed in approximately 6,500 individuals of European and African American ancestry in an external variant database, indicating it is not a common benign variant in these populations. While the K383R variant is a conservative amino acid substitution, which is not likely to impact secondary protein structure, this substitution occurs at a position that is conserved across species. Additionally, in silico analysis predicts this variant is probably damaging to the protein structure/function. Furthermore, a missense variant in this residue (K383N) and missense variants in nearby residues (G377S, G377R, D382Y, A385V, Y386H, Y386C) have been reported in the Human Gene Mutation Database in association with cardiomyopathy (Kuang S et al., 1996; Stenson P et al., 2014), supporting the functional importance of this residue and region of the protein. Therefore, this is a strong candidate for a pathogenic variant, however the possibility that it is a benign variant cannot be excluded.
Laboratory for Molecular Medicine,Partners HealthCare Personalized Medicine RCV000035702 SCV000059353 uncertain significance not specified 2008-03-01 no assertion criteria provided clinical testing

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