rs387906507
|
|
|
0.810 |
GeneticVariation |
UNIPROT |
Two double heterozygous mutations in the F7 gene show different manifestations.
|
12472587 |
2002 |
rs387906507
|
|
|
0.810 |
GeneticVariation |
UNIPROT |
Factor VII deficiency caused by a structural variant N57D of the first epidermal growth factor domain.
|
9414278 |
1998 |
rs387906507
|
|
|
0.810 |
GeneticVariation |
UNIPROT |
A Thr359Met mutation in factor VII of a patient with a hereditary deficiency causes defective secretion of the molecule.
|
8652821 |
1996 |
rs387906507
|
|
|
0.810 |
GeneticVariation |
UNIPROT |
Purification and characterization of factor VII 304-Gln: a variant molecule with reduced activity isolated from a clinically unaffected male.
|
2070047 |
1991 |
rs387906507
|
|
|
0.810 |
GeneticVariation |
UNIPROT |
Topologically equivalent mutations causing dysfunctional coagulation factors VII (294Ala-->Val) and X (334Ser-->Pro).
|
7981691 |
1994 |
rs387906507
|
|
|
0.810 |
GeneticVariation |
UNIPROT |
Molecular analysis of the genotype-phenotype relationship in factor VII deficiency.
|
11129332 |
2000 |
rs387906507
|
|
|
0.810 |
GeneticVariation |
UNIPROT |
Factor VII central. A novel mutation in the catalytic domain that reduces tissue factor binding, impairs activation by factor Xa, and abolishes amidolytic and coagulant activity.
|
8940045 |
1996 |
rs387906507
|
|
|
0.810 |
GeneticVariation |
UNIPROT |
Familial factor VII deficiency with foetal and neonatal fatal cerebral haemorrhage associated with homozygosis to Gly180Arg mutation.
|
19432927 |
2009 |
rs387906507
|
|
|
0.810 |
GeneticVariation |
UNIPROT |
Two new missense mutations (P134T and A244V) in the coagulation factor VII gene.
|
9452082 |
1998 |
rs387906507
|
|
|
0.810 |
GeneticVariation |
UNIPROT |
Detection of missense mutations by single-strand conformational polymorphism (SSCP) analysis in five dysfunctional variants of coagulation factor VII.
|
8242057 |
1993 |
rs387906507
|
|
|
0.810 |
GeneticVariation |
UNIPROT |
A missense mutation (178Cys-->Tyr) and two neutral dimorphisms (115His and 333Ser) in the human coagulation factor VII gene.
|
8364544 |
1993 |
rs387906507
|
|
|
0.810 |
GeneticVariation |
UNIPROT |
Ala244Val is a common, probably ancient mutation causing factor VII deficiency in Moroccan and Iranian Jews.
|
8883260 |
1996 |
rs387906507
|
|
|
0.810 |
GeneticVariation |
UNIPROT |
Molecular defects in CRM+ factor VII deficiencies: modelling of missense mutations in the catalytic domain of FVII.
|
8043443 |
1994 |
rs387906507
|
|
|
0.810 |
GeneticVariation |
UNIPROT |
Recurrent mutations and genotype-phenotype correlations in hereditary factor VII deficiency in Korea.
|
21206266 |
2011 |
rs387906507
|
|
|
0.810 |
GeneticVariation |
UNIPROT |
A patient homozygous for a Gly354Cys mutation in factor VII that results in severely impaired secretion of the molecule, but not complete deficiency.
|
14717781 |
2004 |
rs387906507
|
|
|
0.810 |
GeneticVariation |
UNIPROT |
Phenotypic and genotypic characterization of Factor VII deficiency patients from Western India.
|
19751712 |
2009 |
rs387906507
|
|
|
0.810 |
GeneticVariation |
UNIPROT |
Factor VII Morioka (FVII L-26P): a homozygous missense mutation in the signal sequence identified in a patient with factor VII deficiency.
|
9576180 |
1998 |
rs387906507
|
|
|
0.810 |
GeneticVariation |
UNIPROT |
Mutation pattern in clinically asymptomatic coagulation factor VII deficiency.
|
8844208 |
1996 |
rs387906507
|
|
|
0.810 |
GeneticVariation |
UNIPROT |
Two novel factor VII gene mutations in a Chinese family with factor VII deficiency.
|
11091194 |
2000 |
rs387906507
|
|
|
0.810 |
GeneticVariation |
UNIPROT |
Factor VII deficiency: clinical manifestation of 717 subjects from Europe and Latin America with mutations in the factor 7 gene.
|
18976247 |
2009 |
rs121964926
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
Factor VII Morioka (FVII L-26P): a homozygous missense mutation in the signal sequence identified in a patient with factor VII deficiency.
|
9576180 |
1998 |
rs121964926
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
Factor VII deficiency: clinical manifestation of 717 subjects from Europe and Latin America with mutations in the factor 7 gene.
|
18976247 |
2009 |
rs121964926
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
Two new missense mutations (P134T and A244V) in the coagulation factor VII gene.
|
9452082 |
1998 |
rs121964926
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
Factor VII deficiency caused by a structural variant N57D of the first epidermal growth factor domain.
|
9414278 |
1998 |
rs121964926
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
Two double heterozygous mutations in the F7 gene show different manifestations.
|
12472587 |
2002 |