ClinVar Miner

Submissions for variant NM_001164277.1(SLC37A4):c.1275C>T (p.Ser425=) (rs35010541)

Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 4
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 RCV000224695 SCV000280629 likely benign not provided 2015-05-21 criteria provided, single submitter clinical testing Converted during submission to Likely benign.
GeneDx RCV000128143 SCV000171735 benign not specified 2014-02-09 criteria provided, single submitter clinical testing This variant is considered likely benign or benign based on one or more of the following criteria: it is a conservative change, it occurs at a poorly conserved position in the protein, it is predicted to be benign by multiple in silico algorithms, and/or has population frequency not consistent with disease.
Invitae RCV000543608 SCV000631379 benign Glucose-6-phosphate transport defect 2018-01-12 criteria provided, single submitter clinical testing
PreventionGenetics RCV000128143 SCV000306907 benign not specified 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.