|
Variant ID: 149 |
cDNA Change | c.1159A>G |
|---|---|---|
| Amino Acid Change | p.Met387Val (Legacy AA No. 327) | |
| Type | Point | |
| Effect | Missense | |
| Domain | Serine Protease | |
| Sequence Context | GTG > ATG | |
| Location | Exon( 9) | |
| Minor Allele Frequency (MAF) |
The details of the cases reported with the above variant is as below
| Case ID | Other Variants found in case | Genotype | FVII:C (%) | FVII:Ag (%) | Reported Clinical Severity | Reference | Comments | ||
|---|---|---|---|---|---|---|---|---|---|
| TF-Unknown | TF-Human | TF-Rabbit | |||||||
| 585 | 1 | Heterozygous | 30_<50 | UK | Moderate | Herrmann et al 2009 | |||