Search Results: 1 unique variant retrieved.
Terms with a '*' next to them are explained on the Help Page .
c.3845A>G
p.His1282Arg (Legacy AA No. 1254)
Variant Type:
Point
Domain:
d5B
Location:
Exon 13
Variant Effect:
Missense
Codon Change:
3845A>G
No. of Patients Reported:
1
Phenotype:
NA
Association:
FV Kuwait
Allele Count *:
324
Allele Number *:
282420
Allele Frequency *:
0.001147
References and Comments:
Jadaon et al 2006NA