Search Results: 1 unique variant retrieved.
Terms with a '*' next to them are explained on the Help Page .
c.1160T>C
p.Ile387Thr (Legacy AA No. 359)
Variant Type: 
Point
Domain: 
d5A2
Location: 
Exon 8
Variant Effect: 
Missense
Codon Change: 
1160T>C
No. of Patients Reported: 
5
Phenotype: 
Asymptomatic
Association: 
thrombosis
Allele Count *: 
NA
Allele Number *: 
NA
Allele Frequency *: 
NA
References and Comments:
Mumford et al 2003NA