ClinVar Miner

Submissions for variant NM_001130987.2(DYSF):c.3115dup (p.Glu1039fs)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002637206 SCV003512452 pathogenic Qualitative or quantitative defects of dysferlin 2022-06-04 criteria provided, single submitter clinical testing For these reasons, this variant has been classified as Pathogenic. This premature translational stop signal has been observed in individual(s) with DYSF-related conditions (PMID: 17070050). This variant is not present in population databases (gnomAD no frequency). This sequence change creates a premature translational stop signal (p.Glu1021Glyfs*11) in the DYSF gene. It is expected to result in an absent or disrupted protein product. Loss-of-function variants in DYSF are known to be pathogenic (PMID: 17698709, 20301480).

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