F7
This page contains an overview of the genetic variation in the F7 gene, including its role in inherited cardiac disease. For more details, click on the links below, or for a specific variant, enter the HGVS variant here:
F7 gene and transcript details
Gene Name
coagulation factor VII (serum prothrombin conversion accelerator)
Gene Links
Ensembl: ENSG00000057593 -
Locus Reference Genomic:
Genomic Location
Chromosome 13 : 113,760,156 - 113,773,322 (forward strand)
View in: Ensembl -
UCSC Genome Browser
| Canonical Seqs | Transcript (1398 bases) | Protein (466 aa) |
|---|---|---|
 |
ENST00000375581 | ENSP00000364731 |
 |
||
 |
NM_000131.3 | |
 |
P08709 |
Summary of F7 in Cardiomyopathies
F7 variants in ExAC
Details of the protein-altering F7 variants (missense, loss of function truncating, inframe indels and splice site regions) found in the ExAC database are shown below. To view lists of specific variants with links to detailed population frequency data, click on the variant numbers - for all or a particular variant class.
| Total Variants | Combined frequency of rare variants | |
|---|---|---|
| All Variants | 234 | 0.00433 |
| Truncating | 11 | 0.00020 |
| Missense | 195 | 0.00361 |
| Inframe | 3 | 0.00013 |
| Splice Site | 25 | 0.00038 |