FGF3 AMPLIFICATION Detail (hg38) (FGF3)
Information
Genome
| Assembly | Position |
|---|---|
| hg19 | chr11:69,624,992-69,633,792 View the variant detail on this assembly version. |
| hg38 | chr11:69,810,224-69,819,024 |
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 |
|---|---|---|---|---|---|---|---|---|---|
| breast cancer | Dovitinib | B |
Predictive
|
Supports
|
Sensitivity/Response |
N/A
|
2 | 23658459 | Detail |
DisGeNET
[No Data.]
Annotation
Annotations
| Descrption | Source | Links |
|---|---|---|
| 81 patients were enrolled in a clinical trial with the FGFR inhibitor dovitinib. Four of these patie... | 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
- FGF3
- Genome
- hg38
- Position
- chr11:69,810,224-69,819,024
- Variant Type
- cnv
- Variant (CIViC) (CIViC Variant)
- AMPLIFICATION
- Transcript 1 (CIViC Variant)
- ENST00000334134.2
- Variant URL (CIViC Variant)
- https://civic.genome.wustl.edu/links/variants/630
Genome browser