ClinVar Miner

Submissions for variant NM_001145809.2(MYH14):c.94C>T (p.Arg32Cys)

gnomAD frequency: 0.00001  dbSNP: rs549293063
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
Center for Pediatric Genomic Medicine, Children's Mercy Hospital and Clinics RCV000515053 SCV000610748 uncertain significance not provided 2017-02-22 criteria provided, single submitter clinical testing
CeGaT Center for Human Genetics Tuebingen RCV000515053 SCV004140498 likely benign not provided 2023-10-01 criteria provided, single submitter clinical testing MYH14: BS1

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.