UBB ubiquitin B

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Information
Clinical Significance
Ranking
Frequency
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Information

Symbol: UBB
Type: protein-coding
Description: ubiquitin B
Entrez Gene ID: 7314
Genome: hg19
Position: chr17:16,284,655-16,286,054
Genome: hg38
Position: chr17:16,381,341-16,382,740
MIM: 191339 OMIM
HGNC: HGNC:12463 HGNC
Ensembl: ENSG00000170315 Ensembl
Links: NCBI Gene Cards OncoKB

Clinical Significance

	MGeND	ClinVar
Benign	0	2
Likely benign	0	14
Uncertain significance	0	2

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

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	:
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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	HEL-S-50
MIM	191339 OMIM
HGNC	HGNC:12463 HGNC
Ensembl	ENSG00000170315 Ensembl
AllianceGenome	HGNC:12463

Descrption	Source	Links

ID	Genome	Chromosome	Start	End	Length
ENST00000614404.1	hg38	chr17	16,381,465	16,382,742	1,278
ENST00000395837.1	hg38	chr17	16,381,341	16,382,740	1,400
ENST00000395839.5	hg38	chr17	16,381,290	16,382,740	1,451
ENST00000302182.8	hg38	chr17	16,381,091	16,382,740	1,650
ENST00000535788.1	hg38	chr17	16,381,091	16,382,739	1,649
ENST00000535788.1	hg19	chr17	16,284,405	16,286,053	1,649
ENST00000302182.8	hg19	chr17	16,284,405	16,286,054	1,650
ENST00000395839.5	hg19	chr17	16,284,604	16,286,054	1,451
ENST00000395837.1	hg19	chr17	16,284,655	16,286,054	1,400
ENST00000614404.1	hg19	chr17	16,284,779	16,286,056	1,278

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