ClinVar Miner

Submissions for variant NM_007186.6(CEP250):c.7327del (p.Ter2443SerextTer?)

dbSNP: rs2147242379
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 RCV001916669 SCV002194890 uncertain significance not provided 2023-10-13 criteria provided, single submitter clinical testing This sequence change results in a frameshift in the CEP250 gene (p.*2443Serext*91). While this is not anticipated to result in nonsense mediated decay, it is expected to disrupt the stop codon of the CEP250 protein and extend the protein by 91 additional amino acid residues. This variant is not present in population databases (gnomAD no frequency). This variant has not been reported in the literature in individuals affected with CEP250-related conditions. ClinVar contains an entry for this variant (Variation ID: 1420918). Experimental studies and prediction algorithms are not available or were not evaluated, and the functional significance of this variant is currently unknown. In summary, the available evidence is currently insufficient to determine the role of this variant in disease. Therefore, it has been classified as a Variant of Uncertain Significance.

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.