SEC61B SEC61 translocon subunit beta

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Information
Clinical Significance
Ranking
Frequency
Disease area statistics
Locus Zoom
Variants
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Information

Symbol: SEC61B
Type: protein-coding
Description: SEC61 translocon subunit beta
Entrez Gene ID: 10952
Genome: hg19
Position: chr9:101,984,564-101,992,897
Genome: hg38
Position: chr9:99,222,282-99,230,615
MIM: 609214 OMIM
HGNC: HGNC:16993 HGNC
Ensembl: ENSG00000106803 Ensembl
Links: NCBI Gene Cards OncoKB

Clinical Significance

	MGeND	ClinVar
Benign	0	10
Uncertain significance	0	10

Ranking

	ClinVar
	0
	0
	0
	16
	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
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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

Search Word

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	:
Search word	:
Filtering	:

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
MIM	609214 OMIM
HGNC	HGNC:16993 HGNC
Ensembl	ENSG00000106803 Ensembl
AllianceGenome	HGNC:16993

Descrption	Source	Links

ID	Genome	Chromosome	Start	End	Length
ENST00000498603.5	hg38	chr9	99,222,064	99,230,615	8,552
ENST00000223641.5	hg38	chr9	99,222,282	99,230,615	8,334
ENST00000498603.5	hg19	chr9	101,984,346	101,992,897	8,552
ENST00000223641.5	hg19	chr9	101,984,564	101,992,897	8,334

Key	Value
strand	+
start	101,984,569
Gene Symbol	SEC61B
Entrez GeneId	10,952
Chr Band	9q22.33
end	101,992,900
chr	chr9

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