COPS9 COP9 signalosome subunit 9

Information
Symbol
COPS9
Type
protein-coding
Description
COP9 signalosome subunit 9
Entrez Gene ID
150678
Genome
hg19
Position
chr2:241,065,980-241,075,764
Genome
hg38
Position
chr2:240,126,563-240,136,347
MIM
619349 OMIM
HGNC
HGNC:21314 HGNC
Ensembl
ENSG00000172428 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Uncertain significance 0 2
Ranking
ClinVar
0
0
0
2
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
[No Data.]
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 CSNAP
SYNONYM MYEOV2
MIM 619349 OMIM
HGNC HGNC:21314 HGNC
Ensembl ENSG00000172428 Ensembl
AllianceGenome HGNC:21314
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000307266.7 hg38 chr2 240,126,563 240,136,347 9,785
ENST00000607357.2 hg38 chr2 240,130,828 240,136,305 5,478
ENST00000307266.7 hg19 chr2 241,065,980 241,075,764 9,785
ENST00000607357.2 hg19 chr2 241,070,245 241,075,722 5,478
Genome browser