RNF166 ring finger protein 166

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Information
Clinical Significance
Ranking
Frequency
Disease area statistics
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Information

Symbol: RNF166
Type: protein-coding
Description: ring finger protein 166
Entrez Gene ID: 115992
Genome: hg19
Position: chr16:88,762,909-88,772,816
Genome: hg38
Position: chr16:88,696,501-88,706,408
MIM: 617178 OMIM
HGNC: HGNC:28856 HGNC
Ensembl: ENSG00000158717 Ensembl
Links: NCBI Gene Cards OncoKB

Clinical Significance

	MGeND	ClinVar
Likely benign	0	2
Uncertain significance	0	54

Ranking

	ClinVar
	0
	0
	0
	56
	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
MIM	617178 OMIM
HGNC	HGNC:28856 HGNC
Ensembl	ENSG00000158717 Ensembl
AllianceGenome	HGNC:28856

Descrption	Source	Links

ID	Genome	Chromosome	Start	End	Length
ENST00000567844.1	hg38	chr16	88,697,479	88,706,398	8,920
ENST00000541206.6	hg38	chr16	88,696,536	88,703,617	7,082
ENST00000537718.6	hg38	chr16	88,696,502	88,700,603	4,102
ENST00000312838.9	hg38	chr16	88,696,501	88,706,408	9,908
ENST00000568683.5	hg38	chr16	88,697,394	88,700,056	2,663
ENST00000312838.9	hg19	chr16	88,762,909	88,772,816	9,908
ENST00000537718.6	hg19	chr16	88,762,910	88,767,011	4,102
ENST00000541206.6	hg19	chr16	88,762,944	88,770,025	7,082
ENST00000568683.5	hg19	chr16	88,763,802	88,766,464	2,663
ENST00000567844.1	hg19	chr16	88,763,887	88,772,806	8,920

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