Total submissions: 1
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Invitae | RCV001051739 | SCV001215913 | pathogenic | Qualitative or quantitative defects of dysferlin | 2019-12-29 | criteria provided, single submitter | clinical testing | This variant has not been reported in the literature in individuals with DYSF-related conditions. For these reasons, this variant has been classified as Pathogenic. Loss-of-function variants in DYSF are known to be pathogenic (PMID: 17698709, 20301480). This variant is not present in population databases (ExAC no frequency). This sequence change creates a premature translational stop signal (p.Leu341Phefs*34) in the DYSF gene. It is expected to result in an absent or disrupted protein product. |