Search Results: 1 unique variant retrieved.
Terms with a '*' next to them are explained on the Help Page .
c.1238T>C
p.Met413Thr (Legacy AA No. 385)
Variant Type:
Point
Domain:
d5A2
Location:
Exon 8
Variant Effect:
Missense
Codon Change:
1238T>C
No. of Patients Reported:
2
Phenotype:
NA
Association:
thrombosis
Allele Count *:
21159
Allele Number *:
282730
Allele Frequency *:
0.074838
References and Comments:
de Visser et al 2000NA