Search Results: 1 unique variant retrieved.
Terms with a '*' next to them are explained on the Help Page .
c.355T>A
p.Tyr119Asn (Legacy AA No. 91)
Variant Type:
Point
Domain:
d5A1
Location:
Exon 3
Variant Effect:
Missense
Codon Change:
355T>A
No. of Patients Reported:
1
Phenotype:
Asymptomatic
Association:
FV Deficiency
Allele Count *:
1
Allele Number *:
250208
Allele Frequency *:
0.000004
References and Comments:
Delev et al 2008muscle haematoma and one bleeding episode after delivery