TNFAIP8L3 TNF alpha induced protein 8 like 3

Information
Symbol
TNFAIP8L3
Type
protein-coding
Description
TNF alpha induced protein 8 like 3
Entrez Gene ID
388121
Genome
hg19
Position
chr15:51,348,795-51,397,473
Genome
hg38
Position
chr15:51,056,598-51,105,276
MIM
616438 OMIM
HGNC
HGNC:20620 HGNC
Ensembl
ENSG00000183578 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely benign 0 4
Uncertain significance 0 42
Ranking
ClinVar
0
0
0
46
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 TIPE3
MIM 616438 OMIM
HGNC HGNC:20620 HGNC
Ensembl ENSG00000183578 Ensembl
AllianceGenome HGNC:20620
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000649177.1 hg38 chr15 51,056,677 51,094,501 37,825
ENST00000637513.2 hg38 chr15 51,056,601 51,094,906 38,306
ENST00000327536.5 hg38 chr15 51,056,598 51,105,276 48,679
ENST00000327536.5 hg19 chr15 51,348,795 51,397,473 48,679
ENST00000637513.2 hg19 chr15 51,348,798 51,387,103 38,306
ENST00000649177.1 hg19 chr15 51,348,874 51,386,698 37,825
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