ICOS inducible T cell costimulator

Information
Symbol
ICOS
Type
protein-coding
Description
inducible T cell costimulator
Entrez Gene ID
29851
Genome
hg19
Position
chr2:204,801,486-204,826,300
Genome
hg38
Position
chr2:203,936,763-203,961,577
MIM
604558 OMIM
HGNC
HGNC:5351 HGNC
Ensembl
ENSG00000163600 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Pathogenic 0 14
Likely pathogenic 0 6
Benign 0 52
Likely benign 0 98
Conflicting classifications of pathogenicity 0 22
Uncertain significance 0 142
Ranking
ClinVar
0
0
38
274
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 AILIM
SYNONYM CD278
SYNONYM CVID1
MIM 604558 OMIM
HGNC HGNC:5351 HGNC
Ensembl ENSG00000163600 Ensembl
AllianceGenome HGNC:5351
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000316386.11 hg38 chr2 203,936,763 203,961,577 24,815
ENST00000435193.1 hg38 chr2 203,936,780 203,961,577 24,798
ENST00000316386.11 hg19 chr2 204,801,486 204,826,300 24,815
ENST00000435193.1 hg19 chr2 204,801,503 204,826,300 24,798
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