TNFSF13B TNF superfamily member 13b

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Information
Clinical Significance
Ranking
Frequency
Disease area statistics
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Information

Symbol: TNFSF13B
Type: protein-coding
Description: TNF superfamily member 13b
Entrez Gene ID: 10673
Genome: hg19
Position: chr13:108,922,066-108,960,826
Genome: hg38
Position: chr13:108,269,718-108,308,478
MIM: 603969 OMIM
HGNC: HGNC:11929 HGNC
Ensembl: ENSG00000102524 Ensembl
Links: NCBI Gene Cards OncoKB

Clinical Significance

	MGeND	ClinVar
Benign	0	8
Likely benign	0	2
Uncertain significance	0	8

Ranking

	ClinVar
	0
	0
	0
	18
	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

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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
Variant name	Gene	AA change	CDS	Japanese frequency	TogoVar	Entry	Origin	Type	Annotation	Genome	Entry	Origin	Annotation	CIViC evidence	DisGeNET entry	COSMIC occurrence	Prediction

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Target data	:	MGeND data only
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Name	MGeND				Type	Genome	Size	Chromosome	Start	Stop	Ref	Alt	ClinVar	Origin	Entry	CIViC evidence	DisGeNET entry
Name	Entry	Origin	Type	Annotation	Type	Genome	Size	Chromosome	Start	Stop	Ref	Alt	ClinVar	Origin	Entry	CIViC evidence	DisGeNET entry

Search Word

Target data	:	MGeND data only
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Name	MGeND				Type	Genome	Gene symbol	Chromosome	Genomic start	Genomic stop	Strand	Ref	Alt	ClinVar	Origin	Entry	CIViC evidence	DisGeNET entry
Name	Entry	Origin	Type	Annotation	Type	Genome	Gene symbol	Chromosome	Genomic start	Genomic stop	Strand	Ref	Alt	ClinVar	Origin	Entry	CIViC evidence	DisGeNET entry

Type	ID
SYNONYM	BAFF
SYNONYM	BLYS
SYNONYM	CD257
SYNONYM	DTL
SYNONYM	TALL-1
SYNONYM	TALL1
SYNONYM	THANK
SYNONYM	TNFSF20
SYNONYM	TNLG7A
SYNONYM	ZTNF4
MIM	603969 OMIM
HGNC	HGNC:11929 HGNC
Ensembl	ENSG00000102524 Ensembl
AllianceGenome	HGNC:11929

Descrption	Source	Links

ID	Genome	Chromosome	Start	End	Length
ENST00000430559.5	hg38	chr13	108,269,629	108,308,484	38,856
ENST00000375887.9	hg38	chr13	108,269,718	108,308,478	38,761
ENST00000542136.1	hg38	chr13	108,269,896	108,303,467	33,572
ENST00000430559.5	hg19	chr13	108,921,977	108,960,832	38,856
ENST00000375887.9	hg19	chr13	108,922,066	108,960,826	38,761
ENST00000542136.1	hg19	chr13	108,922,244	108,955,815	33,572

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