FGFR1 FGFR1 FUSIONS Detail (hg38) (FGFR1)
Information
Genome
Assembly | Position |
---|---|
hg19 | chr8:38,268,656-38,325,363 View the variant detail on this assembly version. |
hg38 | chr8:38,411,138-38,467,845 |
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 |
---|---|---|---|---|---|---|---|---|---|
chronic myelomonocytic leukemia | A |
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Negative | Somatic | 5 | 27069254 | Detail | |
hematologic cancer | A |
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Positive | Somatic | 5 | 27069254 | Detail | |
acute myeloid leukemia | Sunitinib,Sorafenib | D |
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Sensitivity/Response | Somatic | 3 | 21482694 | Detail |
DisGeNET
[No Data.]
Annotation
Annotations
Descrption | Source | Links |
---|---|---|
The 2016 World Health Organization guidelines for the classification of myeloid malignancies uses th... | CIViC Evidence | Detail |
The 2016 World Health Organization guidelines for the classification of myeloid malignancies and acu... | CIViC Evidence | Detail |
In a preclinical trial, the AML cell line KG1 with the FGFR1OP2-FGFR1 fusion mutation was treated wi... | CIViC Evidence | Detail |
- Gene
- FGFR1
- Genome
- hg38
- Position
- chr8:38,411,138-38,467,845
- Variant Type
- fusion
- Variant (CIViC) (CIViC Variant)
- FGFR1 FUSIONS
- Transcript 1 (CIViC Variant)
- ENST00000425967.3
- Variant URL (CIViC Variant)
- https://civic.genome.wustl.edu/links/variants/569
Genome browser