Case ID: 583 |
FVII:C% | Human | Rabbit | Unknown |
---|---|---|---|---|
10_<20 | ||||
FVII:Ag% | UK | |||
Reported Clinical Severity | Mild | |||
Comments | ||||
Reference | Herrmann et al 2009 | 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 | |||||||||||
167 | 1 | Heterozygous | Point | Missense | Exon 3 | c.152C>A | 51 | -9 | p.Ala51Asp | Propeptide |