ABL1 ABL1-RCSD Detail (hg19) (ABL1)
Information
Genome
| Assembly | Position |
|---|---|
| hg19 | chr9:133,588,430-133,763,062 |
| hg38 | chr9:130,713,043-130,887,675 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 |
|---|---|---|---|---|---|---|---|---|---|
| Pediatric B-cell Acute Lymphoblastic Leukemia | Imatinib | C |
Predictive
|
Supports
|
Sensitivity/Response | Somatic | 3 | 25207766 | Detail |
DisGeNET
[No Data.]
Annotation
Annotations
| Descrption | Source | Links |
|---|---|---|
| The ABL1-RCSD1 fusion was identified in a 6 yo boy with Ph-like B-ALL and hyperleukocytosis. Followi... | CIViC Evidence | Detail |
- Gene
- ABL1
- Genome
- hg19
- Position
- chr9:133,588,430-133,763,062
- Variant Type
- fusion
- Variant (CIViC) (CIViC Variant)
- ABL1-RCSD
- Variant URL (CIViC Variant)
- https://civic.genome.wustl.edu/links/variants/2680
Genome browser