TNFRSF9 TNF receptor superfamily member 9

Information
Symbol
TNFRSF9
Type
protein-coding
Description
TNF receptor superfamily member 9
Entrez Gene ID
3604
Genome
hg19
Position
chr1:7,975,931-8,000,899
Genome
hg38
Position
chr1:7,915,871-7,940,839
MIM
602250 OMIM
HGNC
HGNC:11924 HGNC
Ensembl
ENSG00000049249 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Pathogenic 0 16
Likely pathogenic 0 6
Benign 0 24
Likely benign 0 134
Conflicting classifications of pathogenicity 0 4
Uncertain significance 0 112
Ranking
ClinVar
0
0
20
264
2
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 4-1BB
SYNONYM CD137
SYNONYM CDw137
SYNONYM ILA
SYNONYM IMD109
MIM 602250 OMIM
HGNC HGNC:11924 HGNC
Ensembl ENSG00000049249 Ensembl
AllianceGenome HGNC:11924
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000377507.8 hg38 chr1 7,915,871 7,940,839 24,969
ENST00000377507.8 hg19 chr1 7,975,931 8,000,899 24,969
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