Search Results: 1 unique variant retrieved.
Terms with a '*' next to them are explained on the Help Page .
c.894C>T
p.Gly298= (Legacy AA No. 258)
Variant Type:
Point
Domain:
Serine protease
Location:
Exon 8
Variant Effect:
Silent
Codon Change:
C>T
No. of Patients Reported:
0
Phenotype:
None
Allele Count *:
-
Allele Number *:
-
Allele Frequency *:
-
References and Comments:
Borhany et al 2018Polymorphism. Silent mutation.