ClinVar Miner

Submissions for variant NM_182961.4(SYNE1):c.10492C>T (p.Gln3498Ter)

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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 RCV002658377 SCV002972144 pathogenic Autosomal recessive ataxia, Beauce type; Emery-Dreifuss muscular dystrophy 4, autosomal dominant 2022-01-08 criteria provided, single submitter clinical testing This sequence change creates a premature translational stop signal (p.Gln3505*) in the SYNE1 gene. It is expected to result in an absent or disrupted protein product. Loss-of-function variants in SYNE1 are known to be pathogenic (PMID: 19542096, 24319099, 27086870). This variant is not present in population databases (gnomAD no frequency). This variant has not been reported in the literature in individuals affected with SYNE1-related conditions. For these reasons, this variant has been classified as Pathogenic.

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