ClinVar Miner

Submissions for variant NM_001303.4(COX10):c.1186G>A (p.Gly396Ser)

gnomAD frequency: 0.00001  dbSNP: rs142336139
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
Baylor Genetics RCV001333920 SCV001526629 uncertain significance Leigh syndrome 2018-08-06 criteria provided, single submitter clinical testing This variant was determined to be of uncertain significance according to ACMG Guidelines, 2015 [PMID:25741868].
Fulgent Genetics, Fulgent Genetics RCV002486334 SCV002788669 uncertain significance Mitochondrial complex 4 deficiency, nuclear type 3 2022-02-03 criteria provided, single submitter 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.