FGFR1 ZNF198-FGFR1 Detail (hg38) (FGFR1)
Information
Genome
| Assembly | Position |
|---|---|
| hg19 | chr8:38,268,656-38,326,352 View the variant detail on this assembly version. |
| hg38 | chr8:38,411,138-38,468,834 |
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 |
|---|---|---|---|---|---|---|---|---|---|
| myeloproliferative neoplasm | Midostaurin | C |
|
|
Sensitivity/Response | Somatic | 4 | 15448205 | Detail |
DisGeNET
[No Data.]
Annotation
Annotations
| Descrption | Source | Links |
|---|---|---|
| A t(8;13)(p11;q12) patient with ZNF198-FGFR1-induced progressive myeloproliferative disorder was tre... | CIViC Evidence | Detail |
- Gene
- FGFR1
- Genome
- hg38
- Position
- chr8:38,411,138-38,468,834
- Variant Type
- fusion
- Variant (CIViC) (CIViC Variant)
- ZNF198-FGFR1
- Variant URL (CIViC Variant)
- https://civic.genome.wustl.edu/links/variants/466
Genome browser