Search Results: 1 unique variant retrieved.
Terms with a '*' next to them are explained on the Help Page .
c.1191T>C
p.Gly397= (Legacy AA No. 379)
Variant Type: 
Point
Domain: 
Serine Protease
Codon Change: 
T>C
Variant Effect: 
Silent
No. of Patients Reported: 
0
Phenotype: 
None
Allele Count *: 
42597
Allele Number *: 
282848
Allele Frequency *: 
0.150600