ENST00000366312.2 MIR5689HG

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Information
Variants
Exon
Other genome
CDS sequence
Amino sequence

Information

Transcript ID: ENST00000366312.2
Genome: hg38
Position: chr6:10,434,329-10,456,781
Strand: +
CDS length: 0
Amino acid length: 0
Gene symbol: MIR5689HG
Gene type: ncRNA
Gene description: MIR5689 host gene
Gene Entrez Gene ID: 106660610

Variants

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MGeND data only All data

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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

Exon

Exon number	Start	Stop
1	10,434,329	10,434,404
2	10,451,903	10,452,056
3	10,452,748	10,452,827
4	10,456,436	10,456,781

Other genome

Genome	Chromosome	Start	End	Links
hg19	chr6	10,434,562	10,457,014	Link

CDS sequence

Amino sequence