|
Variant ID: 991 |
cDNA Change | c.-401G>T |
|---|---|---|
| Amino Acid Change | (Legacy AA No. 0) | |
| Type | Point | |
| Effect | Promoter | |
| Domain | ||
| Sequence Context | ||
| Location | Flanking( 5') | |
| Minor Allele Frequency (MAF) | 0.2041 |
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 | |||||||
| 410 | 7 | Heterozygous | 23 | 24 | asymptomatic | Unpublished Submission | |||