ClinVar Miner

Submissions for variant NM_033380.3(COL4A5):c.956G>A (p.Gly319Asp)

dbSNP: rs104886086
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
Centre for Mendelian Genomics, University Medical Centre Ljubljana RCV000021227 SCV001367436 likely pathogenic X-linked Alport syndrome 2018-11-05 criteria provided, single submitter clinical testing This variant was classified as: Likely pathogenic. The following ACMG criteria were applied in classifying this variant: PM1,PM2,PP3,PP2,PP5.
Fulgent Genetics, Fulgent Genetics RCV000021227 SCV005679795 likely pathogenic X-linked Alport syndrome 2024-04-10 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.