ClinVar Miner

Submissions for variant NM_015512.5(DNAH1):c.7676del (p.Val2559fs)

gnomAD frequency: 0.00001  dbSNP: rs765417610
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
Download table as spreadsheet
Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000655824 SCV000777755 pathogenic Spermatogenic failure 18; Ciliary dyskinesia, primary, 37 2023-11-07 criteria provided, single submitter clinical testing This sequence change creates a premature translational stop signal (p.Val2559Alafs*7) in the DNAH1 gene. It is expected to result in an absent or disrupted protein product. Loss-of-function variants in DNAH1 are known to be pathogenic (PMID: 27573432, 27798045). This variant is present in population databases (rs765417610, gnomAD 0.004%). This variant has not been reported in the literature in individuals affected with DNAH1-related conditions. ClinVar contains an entry for this variant (Variation ID: 544627). For these reasons, this variant has been classified as Pathogenic.
Fulgent Genetics, Fulgent Genetics RCV000655824 SCV002800963 likely pathogenic Spermatogenic failure 18; Ciliary dyskinesia, primary, 37 2022-04-29 criteria provided, single submitter clinical testing

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.