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Case ID: 752 |
FVII:C% | Human | Rabbit | Unknown |
|---|---|---|---|---|
| 11 | ||||
| FVII:Ag% | 11 | |||
| Reported Clinical Severity | Unknown | |||
| Comments | ||||
| Reference | Rizzotto et al 2006 | Common Variant Sites tested and found to be as per the reference sequence in both alleles | ||
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 | |||||||||||
| 11 | 3 | Homozygous | Point | Missense | Exon 1 | c.38T>C | CTT>CCT | 13 | -48 | p.Leu13Pro | Signal Peptide | |