Search Results: 1 unique variant retrieved.



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

  c.1839G>A
p.Glu613= (Legacy AA No. 595)
Variant Type: 
Point
Domain: 
Serine Protease
Codon Change: 
G>A
Variant Effect: 
Silent
No. of Patients Reported: 
0
Phenotype: 
None
Allele Count *: 
15421
Allele Number *: 
282820
Allele Frequency *: 
0.054526

Variant Comments & Reference:

Polymorphism. Zivelin et al 2002, Wiewel-Verschueren et al 2017

Patient Information: Show


Structural Interpretation:

Structural analysis cannot be performed on this (Point | Silent) variant.





Factor XI Variant Database