Search Results: 1 unique variant retrieved.
Terms with a '*' next to them are explained on the Help Page .
c.90G>C
p.Gln30His (Legacy AA No. -11)
Variant Type:
Point
Domain:
Intronic Region
Location:
Variant Effect:
Missense
Codon Change:
G>C
No. of Patients Reported:
0
Phenotype:
None
Allele Count *:
1147
Allele Number *:
282874
Allele Frequency *:
0.004055
References and Comments:
Cargill et al 1999Polymorphism.