TNFSF14 TNF superfamily member 14

Information
Symbol
TNFSF14
Type
protein-coding
Description
TNF superfamily member 14
Entrez Gene ID
8740
Genome
hg19
Position
chr19:6,661,264-6,670,171
Genome
hg38
Position
chr19:6,661,253-6,670,160
MIM
604520 OMIM
HGNC
HGNC:11930 HGNC
Ensembl
ENSG00000125735 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 6
Likely benign 0 4
Uncertain significance 0 18
Ranking
ClinVar
0
0
0
28
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
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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 CD258
SYNONYM HVEML
SYNONYM LIGHT
SYNONYM LTg
MIM 604520 OMIM
HGNC HGNC:11930 HGNC
Ensembl ENSG00000125735 Ensembl
AllianceGenome HGNC:11930
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000599359.1 hg38 chr19 6,664,555 6,670,588 6,034
ENST00000245912.7 hg38 chr19 6,661,253 6,670,117 8,865
ENST00000675206.1 hg38 chr19 6,661,253 6,670,160 8,908
ENST00000245912.7 hg19 chr19 6,661,264 6,670,128 8,865
ENST00000675206.1 hg19 chr19 6,661,264 6,670,171 8,908
ENST00000599359.1 hg19 chr19 6,664,566 6,670,599 6,034
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