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
Links
Type Database ID Link
Gene MIM 136350 OMIM
HGNC 3688 HGNC
Ensembl ENSG00000077782 Ensembl
NCBI NCBI
Gene Cards Gene Cards
OncoKB OncoKB
Type Database ID Link
Variant TogoVar
COSMIC
MONDO
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 Diagnostic Supports Negative Somatic 5 27069254 Detail
hematologic cancer A Diagnostic Supports Positive Somatic 5 27069254 Detail
acute myeloid leukemia Sunitinib,Sorafenib D Predictive Does Not Support Sensitivity/Response Somatic 3 21482694 Detail
DisGeNET
[No Data.]
Annotation

Annotations

DescrptionSourceLinks
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