Search Results: 1 unique variant retrieved.
Terms with a '*' next to them are explained on the Help Page .
c.2350A>G
p.Ser784Gly (Legacy AA No. 756)
Variant Type:
Point
Domain:
d5B
Location:
Exon 13
Variant Effect:
Missense
Codon Change:
2350A>G
No. of Patients Reported:
2
Phenotype:
Asymptomatic
Association:
FV Deficiency
Allele Count *:
NA
Allele Number *:
NA
Allele Frequency *:
NA
References and Comments:
Kuang et al 2001bruising, epistaxis, significant bleeding after trauma