TNFRSF11B TNF receptor superfamily member 11b

Information
Symbol
TNFRSF11B
Type
protein-coding
Description
TNF receptor superfamily member 11b
Entrez Gene ID
4982
Genome
hg19
Position
chr8:119,935,796-119,964,124
Genome
hg38
Position
chr8:118,923,557-118,951,885
MIM
602643 OMIM
HGNC
HGNC:11909 HGNC
Ensembl
ENSG00000164761 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Pathogenic 0 16
Likely pathogenic 0 5
Benign 0 40
Likely benign 0 78
Conflicting classifications of pathogenicity 0 10
Uncertain significance 0 202
Ranking
ClinVar
0
0
70
259
8
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 :
Search word :
Filtering :
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 OCIF
SYNONYM OPG
SYNONYM PDB5
SYNONYM TR1
MIM 602643 OMIM
HGNC HGNC:11909 HGNC
Ensembl ENSG00000164761 Ensembl
AllianceGenome HGNC:11909
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000297350.9 hg38 chr8 118,923,557 118,951,885 28,329
ENST00000297350.9 hg19 chr8 119,935,796 119,964,124 28,329
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