TSBP1 testis expressed basic protein 1

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Information
Clinical Significance
Ranking
Frequency
Disease area statistics
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Information

Symbol: TSBP1
Type: protein-coding
Description: testis expressed basic protein 1
Entrez Gene ID: 10665
Genome: hg19
Position: chr6:32,260,475-32,339,656
Genome: hg38
Position: chr6:32,292,698-32,371,879
MIM: 618151 OMIM
HGNC: HGNC:13922 HGNC
Ensembl: ENSG00000204296 Ensembl
Links: NCBI Gene Cards OncoKB

Clinical Significance

	MGeND	ClinVar
not provided	366	0
Uncertain significance	0	4

Ranking

	ClinVar
	0
	0
	0
	4
	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

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
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
Category	:
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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	C6orf10
SYNONYM	TSBP
MIM	618151 OMIM
HGNC	HGNC:13922 HGNC
Ensembl	ENSG00000204296 Ensembl
AllianceGenome	HGNC:13922

Descrption	Source	Links

ID	Genome	Chromosome	Start	End	Length
ENST00000375015.8	hg38	chr6	32,292,698	32,371,907	79,210
ENST00000533191.6	hg38	chr6	32,292,698	32,371,903	79,206
ENST00000442822.6	hg38	chr6	32,288,526	32,371,899	83,374
ENST00000447241.6	hg38	chr6	32,292,698	32,371,879	79,182
ENST00000527965.5	hg38	chr6	32,292,715	32,371,872	79,158
ENST00000442822.6	hg19	chr6	32,256,303	32,339,676	83,374
ENST00000447241.6	hg19	chr6	32,260,475	32,339,656	79,182
ENST00000533191.6	hg19	chr6	32,260,475	32,339,680	79,206
ENST00000375015.8	hg19	chr6	32,260,475	32,339,684	79,210
ENST00000527965.5	hg19	chr6	32,260,492	32,339,649	79,158

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