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Case ID: 495 |
FVII:C% | Human | Rabbit | Unknown |
|---|---|---|---|---|
| <1 | ||||
| FVII:Ag% | 2 | |||
| Reported Clinical Severity | Moderate | |||
| Comments | ||||
| Reference | Herrmann et al 2000 | 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 | |||||||||||
| 16 | 2 | Homozygous | Point | Missense | Exon 3 | c.190T>C | TTC>CTC | 64 | 4 | p.Phe64Leu | Gla | |