Search Results: 1 unique variant retrieved.



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

  c.1033A>T
p.Lys345* (Legacy AA No. 327)
Variant Type: 
Point
Domain: 
Apple 4
Codon Change: 
A>T
Variant Effect: 
Nonsense
No. of Patients Reported: 
1
Phenotype: 
U
Allele Count *: 
-
Allele Number *: 
-
Allele Frequency *: 
-

Variant Comments & Reference:

Lin et al 2020

Patient Information: Show


Structural Interpretation:

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





Factor XI Variant Database