ZNF274 zinc finger protein 274

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Information
Clinical Significance
Ranking
Frequency
Disease area statistics
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Information

Symbol: ZNF274
Type: protein-coding
Description: zinc finger protein 274
Entrez Gene ID: 10782
Genome: hg19
Position: chr19:58,694,428-58,724,928
Genome: hg38
Position: chr19:58,183,061-58,213,562
MIM: 605467 OMIM
HGNC: HGNC:13068 HGNC
Ensembl: ENSG00000171606 Ensembl
Links: NCBI Gene Cards OncoKB

Clinical Significance

	MGeND	ClinVar
Likely benign	0	2
Uncertain significance	0	14

Ranking

	ClinVar
	0
	0
	0
	16
	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	HFB101
SYNONYM	ZF2
SYNONYM	ZKSCAN19
SYNONYM	ZSCAN51
MIM	605467 OMIM
HGNC	HGNC:13068 HGNC
Ensembl	ENSG00000171606 Ensembl
AllianceGenome	HGNC:13068

Descrption	Source	Links

ID	Genome	Chromosome	Start	End	Length
ENST00000610905.4	hg38	chr19	58,183,454	58,213,552	30,099
ENST00000424679.6	hg38	chr19	58,183,029	58,213,562	30,534
ENST00000617501.5	hg38	chr19	58,183,061	58,213,562	30,502
ENST00000326804.8	hg38	chr19	58,183,427	58,213,552	30,126
ENST00000345813.7	hg38	chr19	58,183,087	58,213,554	30,468
ENST00000424679.6	hg19	chr19	58,694,396	58,724,928	30,533
ENST00000617501.5	hg19	chr19	58,694,428	58,724,928	30,501
ENST00000345813.7	hg19	chr19	58,694,454	58,724,920	30,467
ENST00000326804.8	hg19	chr19	58,694,794	58,724,918	30,125
ENST00000610905.4	hg19	chr19	58,694,821	58,724,918	30,098

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