Search Results: 1 unique variant retrieved.
Terms with a '*' next to them are explained on the Help Page .
c.1465G>C
p.Glu489Gln (Legacy AA No. 461)
Variant Type:
Point
Domain:
d5A2
Location:
Exon 10
Variant Effect:
Missense
Codon Change:
1465G>C
No. of Patients Reported:
1
Phenotype:
Asymptomatic
Association:
thrombosis
Allele Count *:
NA
Allele Number *:
NA
Allele Frequency *:
NA
References and Comments:
Guzman et al 2015NA