Variant ID: 992 |
cDNA Change | c.-402A>G |
---|---|---|
Amino Acid Change | (Legacy AA No. 0) | |
Type | Point | |
Effect | Promoter | |
Domain | ||
Sequence Context | ||
Location | Flanking( 5') | |
Minor Allele Frequency (MAF) | 0.2326 |
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410 | 7 | Heterozygous | 23 | 24 | asymptomatic | Unpublished Submission |