Search Results: 1 unique variant retrieved.
Terms with a '*' next to them are explained on the Help Page .
c.2301A>G
p.Ser767Ser (Legacy AA No. 739)
Variant Type:
Point
Domain:
d5B
Location:
Exon 13
Variant Effect:
Silent
Codon Change:
2301A>G
No. of Patients Reported:
1
Phenotype:
NA
Association:
thrombosis
Allele Count *:
77248
Allele Number *:
282526
Allele Frequency *:
0.273419
References and Comments:
Kostka et al 2000NA