RAF1 AMPLIFICATION Detail (hg19) (RAF1)
Information
Genome
Assembly | Position |
---|---|
hg19 | chr3:12,625,100-12,705,725 |
hg38 | chr3:12,583,601-12,664,226 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
Disease | Drug | EL | ET | ED | CS | VO | TR | Pubmed | Links |
---|---|---|---|---|---|---|---|---|---|
skin melanoma | Paclitaxel,Carboplatin,Sorafenib | B |
![]() |
![]() |
Sensitivity/Response | Somatic | 2 | 26307133 | Detail |
DisGeNET
[No Data.]
Annotation
Annotations
Descrption | Source | Links |
---|---|---|
Retrospective analysis of somatic mutations and copy number changes in 119 patients treated with car... | CIViC Evidence | Detail |
Overlapped Transcript Coordinates
Gene | Transcript ID | Exon Number | Chromosome | Start | Stop | Type | Amino Mutation | Transcript Position | Links |
---|
Overlapped Transcript
Gene | Transcript ID | Chromosome | Start | Stop | Links |
---|
- Gene
- RAF1
- Genome
- hg19
- Position
- chr3:12,625,100-12,705,725
- Variant Type
- cnv
- Variant (CIViC) (CIViC Variant)
- AMPLIFICATION
- Transcript 1 (CIViC Variant)
- ENST00000251849.4
- Variant URL (CIViC Variant)
- https://civic.genome.wustl.edu/links/variants/591
Genome browser