Search Results: 1 unique variant retrieved.
Terms with a '*' next to them are explained on the Help Page .
c.5419G>A
p.Ala1807Thr (Legacy AA No. 1779)
Variant Type: 
Point
Domain: 
d5A3
Location: 
Exon 16
Variant Effect: 
Missense
Codon Change: 
5419G>A
No. of Patients Reported: 
3
Phenotype: 
Asymptomatic
Association: 
FV Deficiency
Allele Count *: 
4
Allele Number *: 
282210
Allele Frequency *: 
0.000014
References and Comments:
Delev et al 2009NA