Total submissions: 1
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Invitae | RCV002564002 | SCV001414470 | pathogenic | Ehlers-Danlos syndrome, classic type, 1 | 2019-08-26 | criteria provided, single submitter | clinical testing | This variant is not present in population databases (ExAC no frequency). For these reasons, this variant has been classified as Pathogenic. Loss-of-function variants in COL5A1 are known to be pathogenic (PMID: 23587214). This variant has not been reported in the literature in individuals with COL5A1-related conditions. This sequence change creates a premature translational stop signal (p.Asp398Glufs*8) in the COL5A1 gene. It is expected to result in an absent or disrupted protein product. |