Search Results: 2 unique variants retrieved



Terms with a '*' next to them are explained on the Help Page .

  c.922A>T
p.Ile308Phe (Legacy AA No. 290)
Variant Type: 
Point
Domain: 
Apple 4
Codon Change: 
A>T
Variant Effect: 
Missense
No. of Patients Reported: 
0
Phenotype: 
None
Allele Count *: 
-
Allele Number *: 
-
Allele Frequency *: 
-

Variant Comments & Reference:

Polymorphism. Cargill et al 1999

Patient Information: Show


Structural Interpretation:

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  c.923T>C
p.Ile308Thr (Legacy AA No. 290)
Variant Type: 
Point
Domain: 
Apple 4
Codon Change: 
T>C
Variant Effect: 
Missense
No. of Patients Reported: 
0
Phenotype: 
None
Allele Count *: 
18
Allele Number *: 
251388
Allele Frequency *: 
0.000072

Variant Comments & Reference:

Polymorphism. Hill et al 2005

Patient Information: Show


Structural Interpretation:

Please click HERE for in-depth variant analysis.





Factor XI Variant Database