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
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
myeloproliferative neoplasm Midostaurin C Predictive Supports Sensitivity/Response Somatic 4 15448205 Detail
DisGeNET
[No Data.]
Annotation

Annotations

DescrptionSourceLinks
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