Case ID: 263 |
FVII:C% | Human | Rabbit | Unknown |
---|---|---|---|---|
<1 | ||||
FVII:Ag% | <1 | |||
Reported Clinical Severity | severe | |||
Comments | ||||
Reference | Peyvandi et al 2000b | 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 | |||||||||||
88 | 6 | 6.74E-5 | Homozygous | Point | Missense | Exon 9 | c.1009C>T | CGC>TGC | 337 | 277 | p.Arg337Cys | Serine Protease |