ClinVar Miner

Submissions for variant NM_001081.3(CUBN):c.4167C>T (p.Tyr1389=) (rs150510291)

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
Illumina Clinical Services Laboratory,Illumina RCV000313610 SCV000361723 uncertain significance Megaloblastic anemia 2016-06-14 criteria provided, single submitter clinical testing
Invitae RCV000816532 SCV000957046 uncertain significance Megaloblastic anemia due to inborn errors of metabolism 2018-09-27 criteria provided, single submitter clinical testing This sequence change affects codon 1389 of the CUBN mRNA. It is a 'silent' change, meaning that it does not change the encoded amino acid sequence of the CUBN protein. This variant is present in population databases (rs150510291, ExAC 0.09%). This variant has not been reported in the literature in individuals with CUBN-related disease. ClinVar contains an entry for this variant (Variation ID: 299482). Algorithms developed to predict the effect of sequence changes on RNA splicing suggest that this variant is not likely to affect RNA splicing, but this prediction has not been confirmed by published transcriptional studies. 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.