RAF1
This page contains an overview of the genetic variation in the RAF1 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:
RAF1 gene and transcript details
Gene Name
v-raf-1 murine leukemia viral oncogene homolog 1
Gene Links
Ensembl: ENSG00000132155 -
Locus Reference Genomic: LRG_413
Genomic Location
Chromosome 3 : 12,626,013 - 12,660,220 (reverse strand)
View in: Ensembl -
UCSC Genome Browser
| Canonical Seqs | Transcript (1944 bases) | Protein (648 aa) |
|---|---|---|
 |
ENST00000251849 | ENSP00000251849 |
 |
LRG_413t1 | LRG_413p1 |
 |
NM_002880.3 | |
 |
P04049 |
Summary of RAF1 in Cardiomyopathies
RAF1 variants in ExAC
Details of the protein-altering RAF1 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 | 173 | 0.00243 |
| Truncating | 4 | 0.00003 |
| Missense | 144 | 0.00188 |
| Inframe | 1 | 0.00001 |
| Splice Site | 24 | 0.00051 |