MIR6889 microRNA 6889

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Information
Clinical Significance
Ranking
Frequency
Disease area statistics
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Information

Symbol: MIR6889
Type: ncRNA
Description: microRNA 6889
Entrez Gene ID: 102466758
Genome: hg38
Position: chr22:41,252,992-41,253,050
HGNC: HGNC:50014 HGNC
Ensembl: ENSG00000274552 Ensembl
Links: NCBI Gene Cards OncoKB

Clinical Significance

	MGeND	ClinVar

Ranking

	ClinVar
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Frequency

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	:
Search word	:
Filtering	:

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	hsa-mir-6889
HGNC	HGNC:50014 HGNC
Ensembl	ENSG00000274552 Ensembl
miRBase	MI0022736
AllianceGenome	HGNC:50014

Descrption	Source	Links

ID	Genome	Chromosome	Start	End	Length
ENST00000613185.1	hg38	chr22	41,252,992	41,253,050	59

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