|
Variant ID: 10 |
cDNA Change | c.27_28delCT |
|---|---|---|
| Amino Acid Change | p.Cys10Profs*16 (Legacy AA No. -51) | |
| Type | Deletion | |
| Effect | Frameshift | |
| Domain | Signal Peptide | |
| Sequence Context | delTC | |
| Location | Exon( 1) | |
| 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 | |||||||
| 282 | 4 | Heterozygous | <1 | <1 | severe | Shen et al 2001 | |||