Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Invitae | RCV001057404 | SCV001221893 | pathogenic | Microcephaly, normal intelligence and immunodeficiency | 2023-10-26 | criteria provided, single submitter | clinical testing | This sequence change creates a premature translational stop signal (p.Ser499*) in the NBN gene. It is expected to result in an absent or disrupted protein product. Loss-of-function variants in NBN are known to be pathogenic (PMID: 9590180, 16415040). This variant is not present in population databases (gnomAD no frequency). This variant has not been reported in the literature in individuals affected with NBN-related conditions. ClinVar contains an entry for this variant (Variation ID: 852729). For these reasons, this variant has been classified as Pathogenic. |
Baylor Genetics | RCV003467785 | SCV004199580 | likely pathogenic | Aplastic anemia | 2023-09-05 | criteria provided, single submitter | clinical testing |