Search Results: 1 unique variant retrieved.
Terms with a '*' next to them are explained on the Help Page .
c.552NA
p.Ser184Ser (Legacy AA No. 156)
Variant Type:
Point
Domain:
d5A1
Location:
Exon 4
Variant Effect:
Silent
Codon Change:
552NA
No. of Patients Reported:
4
Phenotype:
NA
Association:
FV Deficiency
Allele Count *:
76222
Allele Number *:
282662
Allele Frequency *:
0.269658
References and Comments:
Janicki et al 2013NA