|
Variant ID: 98 |
cDNA Change | c.1087C>A |
|---|---|---|
| Amino Acid Change | p.Pro363Thr (Legacy AA No. 303) | |
| 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 | |||||||
| 265 | 1 | Homozygous | <1 | 135 | severe | Peyvandi et al 2000b | |||
| 336 | 1 | Homozygous | <1 | 125.7 | severe | Shen et al 2001 | |||