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Case ID: 281 |
FVII:C% | Human | Rabbit | Unknown |
|---|---|---|---|---|
| 45 | ||||
| FVII:Ag% | ||||
| Reported Clinical Severity | mild | |||
| Comments | ||||
| Reference | Millar 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 | |||||||||||
| 62 | 6 | 4.99E-5 | Heterozygous | Point | Intronic | Intron 7 | c.681+1G>T | CAGgt>CAGtt | 0 | 0 | Splice Junction | |
| 996 | 80 | 0.23 | Homozygous | Insertion | Promoter | 5' Flanking | c.-325_-324insCCTATATCCT | 0 | 0 | |||
| 998 | 116 | 0.1341 | Homozygous | Point | Missense | Exon 9 | c.1238G>A | CGG>CAG | 413 | 353 | p.Arg413Gln | Serine Protease |