ClinVar Miner

Submissions for variant NM_015215.4(CAMTA1):c.2585G>C (p.Gly862Ala)

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
CeGaT Center for Human Genetics Tuebingen RCV003410308 SCV004128106 uncertain significance not provided 2023-10-01 criteria provided, single submitter clinical testing CAMTA1: PM2
Zotz-Klimas Genetics Lab, MVZ Zotz Klimas RCV003222584 SCV003916019 uncertain significance Cerebellar dysfunction with variable cognitive and behavioral abnormalities 2023-04-13 no assertion criteria provided clinical testing

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.