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