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Case ID: 318 |
FVII:C% | Human | Rabbit | Unknown |
|---|---|---|---|---|
| 27 | ||||
| FVII:Ag% | ||||
| Reported Clinical Severity | unknown | |||
| Comments | ||||
| Reference | Wulff 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 | |||||||||||
| 71 | 4 | Heterozygous | Deletion | Frameshift | Intron 8 | c.805+3_805+6del | TGGgtgggtacc>TGGgtacc | 0 | 0 | |||
| 988 | 1 | 0 | Heterozygous | Indel | Intronic | Exon 8 | c.795_805+26[8] | 0 | 0 | Serine Protease | ||
| 993 | 7 | 0.2096 | Heterozygous | Point | Intronic | Intron 1 | c.64+9G>A | 0 | 0 | |||
| 999 | 64 | 0.1419 | Heterozygous | Point | Silent | Exon 6 | c.525C>T | CAC>CAT | 175 | 115 | p.His175= | EGF2 |