|
Case ID: 131 |
FVII:C% | Human | Rabbit | Unknown |
|---|---|---|---|---|
| 5 | ||||
| FVII:Ag% | 44 | |||
| Reported Clinical Severity | asymptomatic | |||
| 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) | |
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 | |||||||||||
| 80 | 38 | 0.0001515 | Heterozygous | Point | Missense | Exon 9 | c.911C>T | GCG>GTG | 304 | 244 | p.Ala304Val | Serine Protease |
| 101 | 59 | 0.000519 | Heterozygous | Point | Missense | Exon 9 | c.1091G>A | CGG>CAG | 364 | 304 | p.Arg364Gln | Serine Protease |
| 990 | 89 | 0.31 | Heterozygous | Indel | Intronic | Exon 8 | c.795_805+26[7] | 0 | 0 | Serine Protease | ||
| 994 | 45 | 0.1342 | Heterozygous | Point | Intronic | Intron 8 | c.806-20G>A | 0 | 0 | |||
| 998 | 116 | 0.1341 | Heterozygous | Point | Missense | Exon 9 | c.1238G>A | CGG>CAG | 413 | 353 | p.Arg413Gln | Serine Protease |