Total submissions: 1
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Invitae | RCV001213439 | SCV001385069 | pathogenic | Primary ciliary dyskinesia | 2023-11-17 | criteria provided, single submitter | clinical testing | This sequence change creates a premature translational stop signal (p.Arg3346*) in the DNAH11 gene. It is expected to result in an absent or disrupted protein product. Loss-of-function variants in DNAH11 are known to be pathogenic (PMID: 18022865, 20513915, 22184204). This variant is present in population databases (rs773851007, gnomAD 0.05%). This premature translational stop signal has been observed in individual(s) with primary ciliary dyskinesia (PMID: 26909801). ClinVar contains an entry for this variant (Variation ID: 943280). For these reasons, this variant has been classified as Pathogenic. |