|
Case ID: 363 |
FVII:C% | Human | Rabbit | Unknown |
|---|---|---|---|---|
| <1 | ||||
| FVII:Ag% | 17 | |||
| Reported Clinical Severity | mild | |||
| Comments | ||||
| Reference | Giansily-Blaizot et al 2001 | Common Variant Sites tested and found to be as per the reference sequence in both alleles | 996(A1A1) 999(H1H1) 998(M1M1) | |
The details of the variants found in this patient are listed below
| Variant ID | No. of Cases | MAF* | Genotype | Type | Effect | Location in gene | Mutation (cDNA) | Sequence Context | Amino Acid | Protein Change | Domain | |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HGVS | Legacy | |||||||||||
| 15 | 1 | Heterozygous | Point | Intronic | Intron 1 | c.131-11G>A | cgc>cac | 0 | 0 | |||
| 27 | 3 | Heterozygous | Point | Intronic | Intron 3 | c.291+1G>A | ACGgt>ACGct | 0 | 0 | Splice Junction | ||
| 994 | 45 | 0.1342 | Homozygous | Point | Intronic | Intron 8 | c.806-20G>A | 0 | 0 | |||