Total submissions: 1
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Invitae | RCV001046662 | SCV001210574 | pathogenic | Primary ciliary dyskinesia | 2019-01-11 | criteria provided, single submitter | clinical testing | For these reasons, this variant has been classified as Pathogenic. Loss-of-function variants in DNAH8 are known to be pathogenic (PMID: 24307375). This variant has not been reported in the literature in individuals with DNAH8-related conditions. This variant is not present in population databases (ExAC no frequency). This sequence change creates a premature translational stop signal (p.Glu1263*) in the DNAH8 gene. It is expected to result in an absent or disrupted protein product. |