ClinVar Miner

Submissions for variant NM_001271208.2(NEB):c.7235A>G (p.Tyr2412Cys) (rs1575122611)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Broad Institute Rare Disease Group,Broad Institute RCV001004940 SCV001164463 uncertain significance Nemaline myopathy 2 2018-12-03 criteria provided, single submitter research The heterozygous p.Tyr2412Cys variant in NEB was identified by our study in the compound heterozygous state, with a likely pathogenic variant, in one individual with nemaline myopathy. The presence of this variant in combination with a reported pathogenic variant and in an individual with nemaline myopathy increases the likelihood that the p.Tyr2412Cys variant is pathogenic. This variant was absent from large population studies. Computational prediction tools and conservation analyses suggest that this variant may affect the protein, though this information is not predictive enough to determine pathogenicity. In summary, the clinical significance of the p.Tyr2412Cys variant is uncertain. ACMG/AMP Criteria applied: PM2, PM3_Supporting, PP3_Supporting (Richards 2015).

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