Search Results: 1 unique variant retrieved.
Terms with a '*' next to them are explained on the Help Page .
c.283G>A
p.Gly95Arg (Legacy AA No. 67)
Variant Type: 
Point
Domain: 
d5A1
Location: 
Exon 3
Variant Effect: 
Missense
Codon Change: 
283G>A
No. of Patients Reported: 
1
Phenotype: 
Asymptomatic
Association: 
FV Deficiency
Allele Count *: 
9
Allele Number *: 
282258
Allele Frequency *: 
0.000032
References and Comments:
Delev et al 2009haematoma