Search Results: 1 unique variant retrieved.
Terms with a '*' next to them are explained on the Help Page .
c.5290A>G
p.Met1764Val (Legacy AA No. 1736)
Variant Type:
Point
Domain:
d5A3
Location:
Exon 16
Variant Effect:
Missense
Codon Change:
5290A>G
No. of Patients Reported:
1
Phenotype:
NA
Association:
thrombosis
Allele Count *:
95163
Allele Number *:
282266
Allele Frequency *:
0.337139
References and Comments:
Chegeni et al 2007NA