TNFSF10 TNF superfamily member 10

Information
Symbol
TNFSF10
Type
protein-coding
Description
TNF superfamily member 10
Entrez Gene ID
8743
Genome
hg19
Position
chr3:172,223,298-172,241,220
Genome
hg38
Position
chr3:172,505,508-172,523,430
MIM
603598 OMIM
HGNC
HGNC:11925 HGNC
Ensembl
ENSG00000121858 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely pathogenic 1 0
Benign 0 14
Likely benign 0 2
Uncertain significance 0 24
Ranking
ClinVar
0
0
0
40
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 :
Search word :
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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 APO2L
SYNONYM Apo-2L
SYNONYM CD253
SYNONYM TANCR
SYNONYM TL2
SYNONYM TNLG6A
SYNONYM TRAIL
MIM 603598 OMIM
HGNC HGNC:11925 HGNC
Ensembl ENSG00000121858 Ensembl
AllianceGenome HGNC:11925
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000420541.6 hg38 chr3 172,505,662 172,523,475 17,814
ENST00000241261.7 hg38 chr3 172,505,508 172,523,430 17,923
ENST00000241261.7 hg19 chr3 172,223,298 172,241,220 17,923
ENST00000420541.6 hg19 chr3 172,223,452 172,241,265 17,814
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