Factor VII Variant Database
Case
ID: 433
FVII:C% Human Rabbit Unknown
2
FVII:Ag% 10
Reported Clinical Severity Mild
Comments
Reference Zhidong et al 2007
Common Variant Sites tested and found to be as per the reference sequence in both alleles

The details of the variants found in this patient are listed below

Variant ID No. of Cases MAF* Genotype Type Effect Location in gene Mutation (cDNA) Sequence Context Amino Acid Protein Change Domain
HGVS Legacy
157 1 Heterozygous Point Missense Exon 9 c.1238G>C 413 353 p.Arg413Pro Serine Protease
173 6 0.0001092 Heterozygous Point Missense Exon 3 c.244T>C 82 22 p.Cys82Arg Gla