Search Results: 1 unique variant retrieved.



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

  c.1812G>T
p.Arg604= (Legacy AA No. 586)
Variant Type: 
Point
Domain: 
Serine Protease
Codon Change: 
G>T
Variant Effect: 
Silent
No. of Patients Reported: 
0
Phenotype: 
None
Allele Count *: 
17400
Allele Number *: 
282854
Allele Frequency *: 
0.061516

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