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Case ID: 771 |
FVII:C% | Human | Rabbit | Unknown |
|---|---|---|---|---|
| 19 | ||||
| FVII:Ag% | UK | |||
| Reported Clinical Severity | Asymptomatic | |||
| Comments | ||||
| Reference | Kwon et al 2011 | 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 | |||||||||||
| 106 | 14 | 4.23E-5 | Heterozygous | Point | Missense | Exon 9 | c.1165T>G | TGT>GGT | 389 | 329 | p.Cys389Gly | Serine Protease |
| 171 | 1 | Heterozygous | Duplication | Inframe | Exon 3 | c.175_180dupCGGCGC | 460 | 400 | p.Arg59_Arg60dup ArgArg | Propeptide | ||