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Case ID: 236 |
FVII:C% | Human | Rabbit | Unknown |
|---|---|---|---|---|
| 1 | ||||
| FVII:Ag% | 1 | |||
| Reported Clinical Severity | asymptomatic | |||
| Comments | ||||
| Reference | Millar et al 2000 | Common Variant Sites tested and found to be as per the reference sequence in both alleles | 996(A1A1) -(C1C1) 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 | |||||||||||
| 8 | 1 | Heterozygous | Point | Missense | Exon 1 | c.3G>C | ATG>ATC | 1 | -60 | p.Met1Ile | Signal Peptide | |
| 59 | 1 | Heterozygous | Deletion | Frameshift | Exon 7 | c.647delG | delG | 216 | 156 | p.Gly216Alafs*17 | Serine Protease | |