Search Results: 1 unique variant retrieved.
Terms with a '*' next to them are explained on the Help Page .
c.2208C>T
p.Ile736Ile (Legacy AA No. 708)
Variant Type:
Point
Domain:
d5a2
Location:
Exon 13
Variant Effect:
Silent
Codon Change:
2208C>T
No. of Patients Reported:
1
Phenotype:
NA
Association:
thrombosis
Allele Count *:
77229
Allele Number *:
282440
Allele Frequency *:
0.273435
References and Comments:
Kostka et al 2000NA