Search Results: 1 unique variant retrieved.



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

  c.801A>G
p.Thr267= (Legacy AA No. 249)
Variant Type: 
Point
Domain: 
Apple 3
Codon Change: 
A>G
Variant Effect: 
Silent
No. of Patients Reported: 
0
Phenotype: 
None
Allele Count *: 
41844
Allele Number *: 
282688
Allele Frequency *: 
0.148022

Variant Comments & Reference:

Frequency in a random sample of normal volunteers is 19%, making this variant a polymorphism. Martincic et al 1998, Ventura et al 2000

Patient Information: Show


Structural Interpretation:

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





Factor XI Variant Database