Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Invitae | RCV001218260 | SCV001390134 | pathogenic | Microcephaly, normal intelligence and immunodeficiency | 2021-10-19 | criteria provided, single submitter | clinical testing | This sequence change creates a premature translational stop signal (p.Tyr322*) 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: 947234). For these reasons, this variant has been classified as Pathogenic. |
Baylor Genetics | RCV003462739 | SCV004191989 | likely pathogenic | Aplastic anemia | 2021-10-19 | criteria provided, single submitter | clinical testing |