ClinVar Miner

Submissions for variant NM_001130144.3(LTBP3):c.2574G>A (p.Leu858=)

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
Labcorp Genetics (formerly Invitae), Labcorp RCV003592662 SCV004263553 uncertain significance Brachyolmia-amelogenesis imperfecta syndrome 2023-06-20 criteria provided, single submitter clinical testing Algorithms developed to predict the effect of sequence changes on RNA splicing suggest that this variant may disrupt the consensus splice site. This variant has not been reported in the literature in individuals affected with LTBP3-related conditions. This variant is present in population databases (rs777391367, gnomAD 0.004%). This sequence change affects codon 858 of the LTBP3 mRNA. It is a 'silent' change, meaning that it does not change the encoded amino acid sequence of the LTBP3 protein. 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.