Factor VII Variant Database
Case
ID: 61
FVII:C% Human Rabbit Unknown
50
FVII:Ag% 87
Reported Clinical Severity asymptomatic
Comments
Reference Bernardi et al 1996
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
95 2 Heterozygous Point Missense Exon 9 c.1072A>G ATG>GTG 358 298 p.Met358Val Serine Protease
990 89 0.31 Heterozygous Indel Intronic Exon 8 c.795_805+26[7] 0 0 Serine Protease
996 80 0.23 Heterozygous Insertion Promoter 5' Flanking c.-325_-324insCCTATATCCT 0 0
998 116 0.1341 Heterozygous Point Missense Exon 9 c.1238G>A CGG>CAG 413 353 p.Arg413Gln Serine Protease