Total submissions: 1
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Invitae | RCV001062456 | SCV001227257 | pathogenic | Retinitis pigmentosa 12; Leber congenital amaurosis 8 | 2022-07-26 | criteria provided, single submitter | clinical testing | This variant is not present in population databases (gnomAD no frequency). For these reasons, this variant has been classified as Pathogenic. ClinVar contains an entry for this variant (Variation ID: 856894). This variant has not been reported in the literature in individuals affected with CRB1-related conditions. This sequence change creates a premature translational stop signal (p.Ala161Profs*45) in the CRB1 gene. It is expected to result in an absent or disrupted protein product. Loss-of-function variants in CRB1 are known to be pathogenic (PMID: 10508521, 22065545, 23379534, 25412400, 26957898, 28041643, 29391521). |