Factor VII Variant Database
Variant
ID: 992
cDNA Change c.-402A>G
Amino Acid Change (Legacy AA No. 0)
Type Point
Effect Promoter
Domain
Sequence Context
Location Flanking( 5')
Minor Allele Frequency (MAF) 0.2326

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
410 7 Heterozygous 23 24 asymptomatic Unpublished Submission