|
Variant ID: 219 |
cDNA Change | c.895A>C |
|---|---|---|
| Amino Acid Change | p.Thr299Pro (Legacy AA No. 239) | |
| Type | Point | |
| Effect | Missense | |
| Domain | Serine Protease | |
| Sequence Context | CCC > ACC | |
| 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 | |||||||
| 419 | 1 | Homozygous | 25 | 95 | Asymptomatic | Borensztajn et al 2005 | |||