ClinVar Miner

List of variants in gene COL4A5 reported as likely benign for Alport syndrome 1, X-linked recessive

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 5
Download table as spreadsheet
NM_033380.3(COL4A5):c.1855C>T (p.Pro619Ser) rs1569494314
NM_033380.3(COL4A5):c.2858G>T (p.Gly953Val) rs78972735
NM_033380.3(COL4A5):c.4200A>G (p.Gly1400=) rs1603318167
NM_033380.3(COL4A5):c.4300C>A (p.Leu1434Met) rs1569508163
NM_033380.3(COL4A5):c.891+9T>G rs779787322

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.