|
Variant ID: 43 |
cDNA Change | c.452G>C |
|---|---|---|
| Amino Acid Change | p.Cys151Ser (Legacy AA No. 91) | |
| Type | Point | |
| Effect | Missense | |
| Domain | EGF2 | |
| Sequence Context | TGT > TCT | |
| Location | Exon( 6) | |
| 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 | |||||||
| 303 | 3 | Homozygous | 1 | 4 | unknown | Millar et al 2000 | |||