ClinVar Miner

Submissions for variant NM_001164508.2(NEB):c.6356_6357del (p.Met2119fs)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Myriad Genetics, Inc. RCV002308295 SCV002601989 likely pathogenic Nemaline myopathy 2 2022-03-15 criteria provided, single submitter clinical testing NM_001271208.1(NEB):c.6356_6357delTG(M2119Tfs*17) is expected to be pathogenic in the context of NEB-related nemaline myopathy. This variant is predicted to lead to an abnormal or absent protein product due to the creation of a premature termination codon in NEB, a gene where loss-of-function variants are known to be pathogenic. Please note: this variant was assessed in the context of healthy population screening.

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