ClinVar Miner

Submissions for variant NM_001805.4(CEBPE):c.842G>A (p.Ser281Asn)

gnomAD frequency: 0.00076  dbSNP: rs149444043
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 3
Download table as spreadsheet
Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000887017 SCV001030554 likely benign Specific granule deficiency 2024-12-24 criteria provided, single submitter clinical testing
New York Genome Center RCV002227502 SCV002506625 uncertain significance Specific granule deficiency 1 2021-05-21 criteria provided, single submitter clinical testing
PreventionGenetics, part of Exact Sciences RCV003424445 SCV004117673 uncertain significance CEBPE-related disorder 2023-09-12 criteria provided, single submitter clinical testing The CEBPE c.842G>A variant is predicted to result in the amino acid substitution p.Ser281Asn. To our knowledge, this variant has not been reported in the literature. This variant is reported in 0.26% of alleles in individuals of African descent in gnomAD (http://gnomad.broadinstitute.org/variant/14-23586700-C-T). At this time, the clinical significance of this variant is uncertain due to the absence of conclusive functional and genetic evidence.

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.