ClinVar Miner

Submissions for variant NM_001277115.2(DNAH11):c.5789A>G (p.Asn1930Ser)

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 RCV002937987 SCV003263087 benign Primary ciliary dyskinesia 2024-10-21 criteria provided, single submitter clinical testing
Ambry Genetics RCV002937987 SCV005577709 uncertain significance Primary ciliary dyskinesia 2024-09-02 criteria provided, single submitter clinical testing The c.5789A>G (p.N1930S) alteration is located in exon 34 (coding exon 34) of the DNAH11 gene. This alteration results from a A to G substitution at nucleotide position 5789, causing the asparagine (N) at amino acid position 1930 to be replaced by a serine (S). Based on insufficient or conflicting evidence, the clinical significance of this alteration remains unclear.

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.