Total submissions: 1
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Invitae | RCV000708336 | SCV000837446 | likely pathogenic | Primary ciliary dyskinesia | 2018-01-17 | criteria provided, single submitter | clinical testing | This variant is an in-frame deletion of the genomic region encompassing exons 48-58 of the DNAH5 gene. It preserves the integrity of the reading frame. This variant has not been reported in the literature in individuals with DNAH5-related disease. Several missense substitutions in this region (p.Ala2881Gly, p.Arg2833His, p.Arg2677Gln) have been determined to be pathogenic (Invitae). This suggests that this region is critical for DNAH5 protein function and that a deletion of this region may also be pathogenic. In summary, the currently available evidence indicates that the variant is pathogenic, but additional data are needed to prove that conclusively. Therefore, this variant has been classified as Likely Pathogenic. |