Total submissions: 1
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Invitae | RCV001226253 | SCV001398560 | pathogenic | Familial aplasia of the vermis; Meckel-Gruber syndrome | 2023-01-15 | 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: 953894). This variant has not been reported in the literature in individuals affected with RPGRIP1L-related conditions. This sequence change creates a premature translational stop signal (p.Glu702*) in the RPGRIP1L gene. It is expected to result in an absent or disrupted protein product. Loss-of-function variants in RPGRIP1L are known to be pathogenic (PMID: 17558409). |