Search Results: 1 unique variant retrieved.
Terms with a '*' next to them are explained on the Help Page .
c.1538G>A
p.Arg513Lys (Legacy AA No. 485)
Variant Type:
Point
Domain:
d5A2
Location:
Exon 10
Variant Effect:
Missense
Codon Change:
1538G>A
No. of Patients Reported:
3
Phenotype:
Asymptomatic
Association:
thrombosis
Allele Count *:
32032
Allele Number *:
282794
Allele Frequency *:
0.11327
References and Comments:
Hiyoshi et al 1998NA