rs121918478
×
Entrez Id:
2147
Gene Symbol:
F2
F2
Inherited Factor II deficiency
0.700
GeneticVariation
UNIPROT
Prothrombin Shanghai: hypoprothrombinaemia caused by substitution of Gla29 by Gly.
14962227
2004
rs121918478
×
Entrez Id:
2147
Gene Symbol:
F2
F2
Inherited Factor II deficiency
0.700
GeneticVariation
UNIPROT
Molecular defect of prothrombin Barcelona. Substitution of cysteine for arginine at residue 273.
3771562
1986
rs121918478
×
Entrez Id:
2147
Gene Symbol:
F2
F2
Inherited Factor II deficiency
0.700
GeneticVariation
UNIPROT
Prothrombin Tokushima, a replacement of arginine-418 by tryptophan that impairs the fibrinogen clotting activity of derived thrombin Tokushima.
3567158
1987
rs121918478
×
Entrez Id:
2147
Gene Symbol:
F2
F2
Inherited Factor II deficiency
0.700
GeneticVariation
UNIPROT
Prothrombin Himi: a compound heterozygote for two dysfunctional prothrombin molecules (Met-337-->Thr and Arg-388-->His).
1421398
1992
rs121918478
×
Entrez Id:
2147
Gene Symbol:
F2
F2
Inherited Factor II deficiency
0.700
GeneticVariation
UNIPROT
Prothrombin Tokushima: characterization of dysfunctional thrombin derived from a variant of human prothrombin.
3801671
1987
rs121918478
×
Entrez Id:
2147
Gene Symbol:
F2
F2
Inherited Factor II deficiency
0.700
GeneticVariation
UNIPROT
Prothrombin Salakta: substitution of glutamic acid-466 by alanine reduces the fibrinogen clotting activity and the esterase activity.
1354985
1992
rs121918478
×
Entrez Id:
2147
Gene Symbol:
F2
F2
Inherited Factor II deficiency
0.700
GeneticVariation
UNIPROT
Identification of the primary structural defect in the dysthrombin thrombin Quick I: substitution of cysteine for arginine-382.
3242619
1988
rs121918478
×
Entrez Id:
2147
Gene Symbol:
F2
F2
Inherited Factor II deficiency
0.700
GeneticVariation
UNIPROT
Substitution of valine for glycine-558 in the congenital dysthrombin thrombin Quick II alters primary substrate specificity.
2719946
1989
rs121918478
×
Entrez Id:
2147
Gene Symbol:
F2
F2
Inherited Factor II deficiency
0.700
GeneticVariation
UNIPROT
Detection of a single base substitution of the gene for prothrombin Tokushima. The application of PCR-SSCP for the genetic and molecular analysis of dysprothrombinemia.
1349838
1992
rs121918478
×
Entrez Id:
2147
Gene Symbol:
F2
F2
Inherited Factor II deficiency
0.700
GeneticVariation
UNIPROT
Prothrombin Frankfurt: a dysfunctional prothrombin characterized by substitution of Glu-466 by Ala.
7792730
1995
rs121918478
×
Entrez Id:
2147
Gene Symbol:
F2
F2
Inherited Factor II deficiency
0.700
GeneticVariation
UNIPROT
Determination of the amino acid substitution in human prothrombin type 3 (157 Glu leads to Lys) and the localization of a third thrombin cleavage site.
6405779
1983
rs121918478
×
Entrez Id:
2147
Gene Symbol:
F2
F2
Inherited Factor II deficiency
0.700
GeneticVariation
UNIPROT
Prothrombin Padua I: incomplete activation due to an amino acid substitution at a factor Xa cleavage site.
7865694
1994