TNFSF9 TNF superfamily member 9

Information
Symbol
TNFSF9
Type
protein-coding
Description
TNF superfamily member 9
Entrez Gene ID
8744
Genome
hg19
Position
chr19:6,531,037-6,535,935
Genome
hg38
Position
chr19:6,531,026-6,535,924
MIM
606182 OMIM
HGNC
HGNC:11939 HGNC
Ensembl
ENSG00000125657 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 2
Likely benign 0 4
Uncertain significance 0 22
Ranking
ClinVar
0
0
0
26
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 :
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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 4-1BB-L
SYNONYM CD137L
SYNONYM TNLG5A
MIM 606182 OMIM
HGNC HGNC:11939 HGNC
Ensembl ENSG00000125657 Ensembl
AllianceGenome HGNC:11939
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000245817.5 hg38 chr19 6,531,026 6,535,924 4,899
ENST00000245817.5 hg19 chr19 6,531,037 6,535,935 4,899
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