ClinVar Miner

Submissions for variant NM_001081.4(CUBN):c.813C>T (p.Pro271=)

gnomAD frequency: 0.00021  dbSNP: rs139348777
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 RCV000866325 SCV001007404 likely benign Imerslund-Grasbeck syndrome 2024-10-26 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002495259 SCV002799097 likely benign Imerslund-Grasbeck syndrome type 1; Proteinuria, chronic benign 2021-07-21 criteria provided, single submitter clinical testing
PreventionGenetics, part of Exact Sciences RCV004742663 SCV005348296 likely benign CUBN-related disorder 2024-04-23 no assertion criteria provided clinical testing This variant is classified as likely benign based on ACMG/AMP sequence variant interpretation guidelines (Richards et al. 2015 PMID: 25741868, with internal and published modifications).

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.