ClinVar Miner

List of variants in gene F11 reported as uncertain significance for Plasma factor XI deficiency

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 23
Download table as spreadsheet
HGVS dbSNP
NM_000128.3(F11):c.1028+9T>C rs376630194
NM_000128.3(F11):c.1200G>A (p.Pro400=) rs150377265
NM_000128.3(F11):c.1431C>T (p.Ser477=) rs149568223
NM_000128.4(F11):c.-459A>G
NM_000128.4(F11):c.1001C>T (p.Pro334Leu)
NM_000128.4(F11):c.1011A>G (p.Ala337=)
NM_000128.4(F11):c.1028+9T>G
NM_000128.4(F11):c.1059C>T (p.Asn353=)
NM_000128.4(F11):c.1174A>G (p.Thr392Ala)
NM_000128.4(F11):c.1579A>G (p.Lys527Glu)
NM_000128.4(F11):c.1609A>T (p.Ile537Leu)
NM_000128.4(F11):c.1625A>G (p.Asn542Ser)
NM_000128.4(F11):c.1683C>T (p.Ala561=)
NM_000128.4(F11):c.1709C>G (p.Ala570Gly)
NM_000128.4(F11):c.1716+10del
NM_000128.4(F11):c.1767G>T (p.Leu589=)
NM_000128.4(F11):c.291G>A (p.Gly97=)
NM_000128.4(F11):c.486-10T>A rs370991682
NM_000128.4(F11):c.536C>T (p.Thr179Met)
NM_000128.4(F11):c.56-6T>C
NM_000128.4(F11):c.596-6G>A rs369721182
NM_000128.4(F11):c.696T>C (p.His232=) rs746382259
NM_000128.4(F11):c.852G>C (p.Arg284Ser)

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.