TNFRSF13B TNF receptor superfamily member 13B

Information
Symbol
TNFRSF13B
Type
protein-coding
Description
TNF receptor superfamily member 13B
Entrez Gene ID
23495
Genome
hg19
Position
chr17:16,842,395-16,875,432
Genome
hg38
Position
chr17:16,939,081-16,972,118
MIM
604907 OMIM
HGNC
HGNC:18153 HGNC
Ensembl
ENSG00000240505 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Pathogenic 0 46
Likely pathogenic 0 16
Benign 0 42
Likely benign 0 178
Conflicting classifications of pathogenicity 0 26
Conflicting classifications of pathogenicity; risk factor 0 2
not provided 2 0
Uncertain significance 0 354
Ranking
ClinVar
0
0
148
462
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
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 CD267
SYNONYM CVID
SYNONYM CVID2
SYNONYM IGAD2
SYNONYM RYZN
SYNONYM TACI
SYNONYM TNFRSF14B
MIM 604907 OMIM
HGNC HGNC:18153 HGNC
Ensembl ENSG00000240505 Ensembl
AllianceGenome HGNC:18153
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000583789.1 hg38 chr17 16,939,444 16,972,087 32,644
ENST00000579315.5 hg38 chr17 16,933,065 16,972,118 39,054
ENST00000261652.7 hg38 chr17 16,939,081 16,972,118 33,038
ENST00000579315.5 hg19 chr17 16,836,379 16,875,432 39,054
ENST00000261652.7 hg19 chr17 16,842,395 16,875,432 33,038
ENST00000583789.1 hg19 chr17 16,842,758 16,875,401 32,644
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