TNFSF8 TNF superfamily member 8

Information
Symbol
TNFSF8
Type
protein-coding
Description
TNF superfamily member 8
Entrez Gene ID
944
Genome
hg19
Position
chr9:117,663,425-117,692,871
Genome
hg38
Position
chr9:114,901,145-114,930,591
MIM
603875 OMIM
HGNC
HGNC:11938 HGNC
Ensembl
ENSG00000106952 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely pathogenic 1 0
Likely benign 0 4
not provided 65 0
Uncertain significance 0 14
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 :
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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 CD153
SYNONYM CD30L
SYNONYM CD30LG
SYNONYM TNLG3A
MIM 603875 OMIM
HGNC HGNC:11938 HGNC
Ensembl ENSG00000106952 Ensembl
AllianceGenome HGNC:11938
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000223795.3 hg38 chr9 114,901,145 114,930,591 29,447
ENST00000618336.4 hg38 chr9 114,893,343 114,930,595 37,253
ENST00000618336.4 hg19 chr9 117,655,623 117,692,875 37,253
ENST00000223795.3 hg19 chr9 117,663,425 117,692,871 29,447
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