|
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| 410 | 7 | Heterozygous | 23 | 24 | asymptomatic | Unpublished Submission | |||