ClinVar Miner

Submissions for variant NM_000488.4(SERPINC1):c.21A>T (p.Gly7=)

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 RCV003030907 SCV003313171 uncertain significance Hereditary antithrombin deficiency 2022-05-13 criteria provided, single submitter clinical testing This variant has not been reported in the literature in individuals affected with SERPINC1-related conditions. This sequence change affects codon 7 of the SERPINC1 mRNA. It is a 'silent' change, meaning that it does not change the encoded amino acid sequence of the SERPINC1 protein. This variant is not present in population databases (gnomAD no frequency). Algorithms developed to predict the effect of sequence changes on RNA splicing suggest that this variant may create or strengthen a splice site. 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.