Factor VII Variant Database
Variant
ID: 92
cDNA Change c.1033G>A
Amino Acid Change p.Gly345Ser (Legacy AA No. 285)
Type Point
Effect Missense
Domain Serine Protease
Sequence Context GGC > AGC
Location Exon( 9)
Minor Allele Frequency (MAF)

The details of the cases reported with the above variant is as below

Case ID Other Variants found in case Genotype FVII:C (%) FVII:Ag (%) Reported Clinical Severity Reference Comments
TF-Unknown TF-Human TF-Rabbit
165 2 Heterozygous unknown Kavlie et al 1997