ZNF567 zinc finger protein 567

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Information
Clinical Significance
Ranking
Frequency
Disease area statistics
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Information

Symbol: ZNF567
Type: protein-coding
Description: zinc finger protein 567
Entrez Gene ID: 163081
Genome: hg19
Position: chr19:37,178,530-37,212,229
Genome: hg38
Position: chr19:36,687,628-36,721,327
HGNC: HGNC:28696 HGNC
Ensembl: ENSG00000189042 Ensembl
Links: NCBI Gene Cards OncoKB

Clinical Significance

	MGeND	ClinVar
Likely benign	0	2
Uncertain significance	0	30

Ranking

	ClinVar
	0
	0
	0
	32
	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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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

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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
HGNC	HGNC:28696 HGNC
Ensembl	ENSG00000189042 Ensembl
AllianceGenome	HGNC:28696

Descrption	Source	Links

ID	Genome	Chromosome	Start	End	Length
ENST00000585696.5	hg38	chr19	36,711,240	36,721,321	10,082
ENST00000682579.1	hg38	chr19	36,687,612	36,721,336	33,725
ENST00000360729.8	hg38	chr19	36,689,400	36,721,326	31,927
ENST00000536254.6	hg38	chr19	36,687,628	36,721,327	33,700
ENST00000588311.5	hg38	chr19	36,703,681	36,723,346	19,666
ENST00000682579.1	hg19	chr19	37,178,514	37,212,238	33,725
ENST00000536254.6	hg19	chr19	37,178,530	37,212,229	33,700
ENST00000360729.8	hg19	chr19	37,180,302	37,212,228	31,927
ENST00000588311.5	hg19	chr19	37,194,583	37,214,248	19,666
ENST00000585696.5	hg19	chr19	37,202,142	37,212,223	10,082

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