C6orf52 chromosome 6 open reading frame 52

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Clinical Significance
Ranking
Frequency
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Information

Symbol: C6orf52
Type: protein-coding
Description: chromosome 6 open reading frame 52
Entrez Gene ID: 347744
Genome: hg19
Position: chr6:10,671,655-10,694,849
Genome: hg38
Position: chr6:10,671,422-10,694,616
HGNC: HGNC:20881 HGNC
Ensembl: ENSG00000137434 Ensembl
Links: NCBI Gene Cards OncoKB

Clinical Significance

	MGeND	ClinVar
Uncertain significance	0	4

Ranking

	ClinVar
	0
	0
	0
	4
	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
HGNC	HGNC:20881 HGNC
Ensembl	ENSG00000137434 Ensembl
AllianceGenome	HGNC:20881

Descrption	Source	Links

ID	Genome	Chromosome	Start	End	Length
ENST00000503680.1	hg38	chr6	10,671,422	10,694,797	23,376
ENST00000379586.5	hg38	chr6	10,671,422	10,694,609	23,188
ENST00000426700.6	hg38	chr6	10,671,422	10,687,550	16,129
ENST00000460742.6	hg38	chr6	10,671,418	10,694,533	23,116
ENST00000259983.8	hg38	chr6	10,671,422	10,694,616	23,195
ENST00000460742.6	hg19	chr6	10,671,651	10,694,766	23,116
ENST00000426700.6	hg19	chr6	10,671,655	10,687,783	16,129
ENST00000379586.5	hg19	chr6	10,671,655	10,694,842	23,188
ENST00000259983.8	hg19	chr6	10,671,655	10,694,849	23,195
ENST00000503680.1	hg19	chr6	10,671,655	10,695,030	23,376

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