ClinVar Miner

Submissions for variant NM_006118.3(HAX1):c.407del (p.His136fs)

Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 1
Download table as spreadsheet
Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000816591 SCV000957108 pathogenic Severe congenital neutropenia 3, autosomal recessive 2018-09-28 criteria provided, single submitter clinical testing This sequence change creates a premature translational stop signal (p.His136Profs*78) in the HAX1 gene. It is expected to result in an absent or disrupted protein product. The frequency data for this variant in the population databases is considered unreliable, as metrics indicate poor data quality at this position in the ExAC database. This variant has not been reported in the literature in individuals with HAX1-related disease. Loss-of-function variants in HAX1 are known to be pathogenic (PMID: 17187068). For these reasons, this variant has been classified as Pathogenic.

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.