BRAF WASFL-BRAF Fusion Detail (hg19) (BRAF)
Information
Genome
| Assembly | Position |
|---|---|
| hg19 | chr7:140,419,127-140,624,729 |
| hg38 | chr7:140,719,327-140,924,929 View the variant detail on this assembly version. |
Summary
MGeND
| Clinical significance | |
| Variant entry | |
| GWAS entry | |
| Disease area statistics | Show details |
ClinVar
| Clinical Significance | |
| Review star | [No Data.] |
| Show details | |
Disease area statistics
[No Data.]
MGeND
[No Data.]
ClinVar
[No Data.]
CIViC
DisGeNET
[No Data.]
Annotation
Annotations
| Descrption | Source | Links |
|---|---|---|
| The phase 2a MyPathway study assigned patients with HER2, EGFR, BRAF or SHH alterations to treatment... | CIViC Evidence | Detail |
- Gene
- BRAF
- Genome
- hg19
- Position
- chr7:140,419,127-140,624,729
- Variant Type
- fusion
- Variant (CIViC) (CIViC Variant)
- WASFL-BRAF Fusion
- Variant URL (CIViC Variant)
- https://civic.genome.wustl.edu/links/variants/2228
- Variant (CIViC) (CIViC Variant)
- FAM73A-BRAF fusion
- Variant URL (CIViC Variant)
- https://civic.genome.wustl.edu/links/variants/2987
Genome browser