Search Results: 1 unique variant retrieved.
Terms with a '*' next to them are explained on the Help Page .
c.1707C>T
p.Asp569= (Legacy AA No. 551)
Variant Type: 
Point
Domain: 
Serine Protease
Codon Change: 
C>T
Variant Effect: 
Silent
No. of Patients Reported: 
0
Phenotype: 
None
Allele Count *: 
4190
Allele Number *: 
282698
Allele Frequency *: 
0.014821