Search Results: 1 unique variant retrieved.
Terms with a '*' next to them are explained on the Help Page .
c.776G>A
p.Gly259Glu (Legacy AA No. 231)
Variant Type: 
Point
Domain: 
d5A1
Location: 
Exon 6
Variant Effect: 
Missense
Codon Change: 
776G>A
No. of Patients Reported: 
2
Phenotype: 
Mild
Association: 
FV Deficiency
Allele Count *: 
NA
Allele Number *: 
NA
Allele Frequency *: 
NA
References and Comments:
Cutler et al 2010NA