CYB561D2 cytochrome b561 family member D2

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Information
Clinical Significance
Ranking
Frequency
Disease area statistics
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Information

Symbol: CYB561D2
Type: protein-coding
Description: cytochrome b561 family member D2
Entrez Gene ID: 11068
Genome: hg19
Position: chr3:50,388,289-50,391,463
Genome: hg38
Position: chr3:50,350,858-50,354,032
MIM: 607068 OMIM
HGNC: HGNC:30253 HGNC
Ensembl: ENSG00000114395 Ensembl
Links: NCBI Gene Cards OncoKB

Clinical Significance

	MGeND	ClinVar
Benign	0	4
Likely benign	0	2
Uncertain significance	0	14

Ranking

	ClinVar
	0
	0
	0
	20
	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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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

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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	101F6
SYNONYM	TSCytb
SYNONYM	TSP10
SYNONYM	XXcos-LUCA11.4
MIM	607068 OMIM
HGNC	HGNC:30253 HGNC
Ensembl	ENSG00000114395 Ensembl
AllianceGenome	HGNC:30253

Descrption	Source	Links

ID	Genome	Chromosome	Start	End	Length
ENST00000425346.6	hg38	chr3	50,350,862	50,354,069	3,208
ENST00000232508.9	hg38	chr3	50,350,845	50,354,069	3,225
ENST00000418577.1	hg38	chr3	50,350,858	50,354,032	3,175
ENST00000424512.5	hg38	chr3	50,350,845	50,354,052	3,208
ENST00000424512.5	hg19	chr3	50,388,276	50,391,483	3,208
ENST00000232508.9	hg19	chr3	50,388,276	50,391,500	3,225
ENST00000418577.1	hg19	chr3	50,388,289	50,391,463	3,175
ENST00000425346.6	hg19	chr3	50,388,293	50,391,500	3,208

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