Total submissions: 1
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Labcorp Genetics |
RCV001950813 | SCV002235002 | pathogenic | Sphingolipid activator protein 1 deficiency | 2022-04-08 | criteria provided, single submitter | clinical testing | This sequence change creates a premature translational stop signal (p.Gln402*) in the PSAP gene. It is expected to result in an absent or disrupted protein product. Loss-of-function variants in PSAP are known to be pathogenic (PMID: 8554069, 11309366, 17616409, 19267410, 30632081). This variant is not present in population databases (gnomAD no frequency). This variant has not been reported in the literature in individuals affected with PSAP-related conditions. For these reasons, this variant has been classified as Pathogenic. |