Search Results: 1 unique variant retrieved.
Terms with a '*' next to them are explained on the Help Page .
c.286G>C
p.Asp96His (Legacy AA No. 68)
Variant Type:
Point
Domain:
d5A1
Location:
Exon 3
Variant Effect:
Missense
Codon Change:
286G>C
No. of Patients Reported:
16
Phenotype:
Moderate
Association:
FV Deficiency
Allele Count *:
22
Allele Number *:
282272
Allele Frequency *:
0.000078
References and Comments:
Cao et al 2011bleeding during teeth regeneration prolonged