TNFRSF1B TNF receptor superfamily member 1B

Information
Symbol
TNFRSF1B
Type
protein-coding
Description
TNF receptor superfamily member 1B
Entrez Gene ID
7133
Genome
hg19
Position
chr1:12,227,048-12,269,277
Genome
hg38
Position
chr1:12,166,991-12,209,220
MIM
191191 OMIM
HGNC
HGNC:11917 HGNC
Ensembl
ENSG00000028137 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 10
Likely benign 0 8
Uncertain significance 0 30
Ranking
ClinVar
0
0
0
44
4
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 CD120b
SYNONYM TBPII
SYNONYM TNF-R-II
SYNONYM TNF-R75
SYNONYM TNFBR
SYNONYM TNFR1B
SYNONYM TNFR2
SYNONYM TNFR80
SYNONYM p75
SYNONYM p75TNFR
MIM 191191 OMIM
HGNC HGNC:11917 HGNC
Ensembl ENSG00000028137 Ensembl
AllianceGenome HGNC:11917
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000536782.2 hg38 chr1 12,167,003 12,192,358 25,356
ENST00000376259.7 hg38 chr1 12,166,991 12,209,220 42,230
ENST00000376259.7 hg19 chr1 12,227,048 12,269,277 42,230
ENST00000536782.2 hg19 chr1 12,227,060 12,252,415 25,356
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