ClinVar Miner

Submissions for variant NM_001164508.2(NEB):c.4326C>T (p.Ser1442=)

gnomAD frequency: 0.00001  dbSNP: rs1196827078
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000527172 SCV000640798 likely benign Nemaline myopathy 2 2024-01-19 criteria provided, single submitter clinical testing
PreventionGenetics, part of Exact Sciences RCV004553216 SCV004769145 likely benign NEB-related disorder 2019-07-10 no assertion criteria provided clinical testing This variant is classified as likely benign based on ACMG/AMP sequence variant interpretation guidelines (Richards et al. 2015 PMID: 25741868, with internal and published modifications).

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