ClinVar Miner

List of variants reported as pathogenic for Factor X deficiency

Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 14
Download table as spreadsheet
HGVS dbSNP
F10, ASP282ASN
F10, G-A, -20
F10, GLU14LYS
F10, GLU32GLN
F10, GLU7GLY
F10, PRO343SER
F10, SER334PRO
F10, THR318MET
F10, VAL298MET
Factor X Ketchikan
NM_000504.4(F10):c.1096C>T (p.Arg366Cys) rs104894392
NM_000504.4(F10):c.424G>A (p.Glu142Lys) rs61753266
NM_000504.4(F10):c.814del (p.Ile271_Leu272insTer) rs387906506
NM_000504.4(F10):c.859A>T (p.Arg287Trp) rs121964948

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.