FGFR1OP2 FGFR1 oncogene partner 2

Information
Symbol
FGFR1OP2
Type
protein-coding
Description
FGFR1 oncogene partner 2
Entrez Gene ID
26127
Genome
hg19
Position
chr12:27,091,403-27,119,581
Genome
hg38
Position
chr12:26,938,470-26,966,648
MIM
608858 OMIM
HGNC
HGNC:23098 HGNC
Ensembl
ENSG00000111790 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely benign 0 2
not provided 1 0
Uncertain significance 0 16
Ranking
ClinVar
0
0
0
18
0
Frequency
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
Disease area statistics
Locus Zoom
Variants
Search Word
Target data :
MGeND data only
Category :
Search word :
Filtering :
Variant name Gene AA change CDS Japanese
frequency		 TogoVar MGeND Genome ClinVar CIViC evidence DisGeNET entry COSMIC
occurrence		 Prediction
Entry Origin Type Annotation Entry Origin Annotation
Search Word
Target data :
MGeND data only
Category :
Search word :
Filtering :
Name MGeND Type Genome Size Chromosome Start Stop Ref Alt ClinVar Origin Entry CIViC evidence DisGeNET entry
Entry Origin Type Annotation
Search Word
Target data :
MGeND data only
Category :
Search word :
Filtering :
Name MGeND Type Genome Gene symbol Chromosome Genomic start Genomic stop Strand Ref Alt ClinVar Origin Entry CIViC evidence DisGeNET entry
Entry Origin Type Annotation
TypeID
SYNONYM HSPC123-like
SYNONYM WIT3.0
MIM 608858 OMIM
HGNC HGNC:23098 HGNC
Ensembl ENSG00000111790 Ensembl
AllianceGenome HGNC:23098
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000229395.8 hg38 chr12 26,938,470 26,966,648 28,179
ENST00000327214.5 hg38 chr12 26,938,500 26,966,650 28,151
ENST00000546072.5 hg38 chr12 26,938,497 26,960,846 22,350
ENST00000229395.8 hg19 chr12 27,091,403 27,119,581 28,179
ENST00000546072.5 hg19 chr12 27,091,430 27,113,779 22,350
ENST00000327214.5 hg19 chr12 27,091,433 27,119,583 28,151
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