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Case ID: 358 |
FVII:C% | Human | Rabbit | Unknown |
|---|---|---|---|---|
| <1 | ||||
| FVII:Ag% | 132 | |||
| 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 | |||||||||||
| 122 | 3 | Homozygous | Point | Missense | Exon 9 | c.1272G>C | TGG>TGC | 424 | 364 | p.Trp424Cys | Serine Protease | |