ClinVar Miner

List of variants in gene FBP1 reported as likely benign for carbohydrate metabolism disease

Included ClinVar conditions (161):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 12
Download table as spreadsheet
HGVS dbSNP
NM_000507.4(FBP1):c.*248del rs11351544
NM_000507.4(FBP1):c.102G>C (p.Leu34=) rs143832764
NM_000507.4(FBP1):c.306C>T (p.His102=) rs776366063
NM_000507.4(FBP1):c.495C>T (p.Tyr165=)
NM_000507.4(FBP1):c.498A>C (p.Ala166=)
NM_000507.4(FBP1):c.639C>T (p.Asn213=)
NM_000507.4(FBP1):c.663C>T (p.Asp221=)
NM_000507.4(FBP1):c.670G>A (p.Val224Ile) rs140222720
NM_000507.4(FBP1):c.697T>A (p.Phe233Ile) rs2297085
NM_000507.4(FBP1):c.745A>C (p.Met249Leu)
NM_000507.4(FBP1):c.826-9G>C rs200948424
NM_000507.4(FBP1):c.915C>T (p.Asp305=) rs762285012

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.