Total submissions: 1
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Invitae | RCV001219184 | SCV001391109 | pathogenic | Primary ciliary dyskinesia | 2019-08-22 | criteria provided, single submitter | clinical testing | This variant is a deletion of the genomic region encompassing exons 23-27 and part of exon 28 (c.3396+1997_4506del) of the DNAH5 gene. It is expected to disrupt RNA splicing and likely results in an absent or disrupted protein product. This variant has been observed in individual(s) with primary ciliary dyskinesia (Invitae). In at least one individual the data is consistent with the variant being in trans (on the opposite chromosome) from a pathogenic variant. Loss-of-function variants in DNAH5 are known to be pathogenic (PMID: 11788826, 16627867). For these reasons, this variant has been classified as Pathogenic. |