Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Invitae | RCV001052644 | SCV001216865 | pathogenic | Hereditary spastic paraplegia 4 | 2019-12-11 | criteria provided, single submitter | clinical testing | For these reasons, this variant has been classified as Pathogenic. Loss-of-function variants in SPAST are known to be pathogenic (PMID: 20932283). This variant has not been reported in the literature in individuals with SPAST-related conditions. This variant is not present in population databases (ExAC no frequency). This sequence change creates a premature translational stop signal (p.Glu464*) in the SPAST gene. It is expected to result in an absent or disrupted protein product. |
Genome Diagnostics Laboratory, |
RCV001847137 | SCV002105608 | pathogenic | Hereditary spastic paraplegia | 2021-11-17 | criteria provided, single submitter | clinical testing |