MIR5689 microRNA 5689

Information
Symbol
MIR5689
Type
ncRNA
Description
microRNA 5689
Entrez Gene ID
100846998
Genome
hg19
Position
chr6:10,439,950-10,440,027
Genome
hg38
Position
chr6:10,439,717-10,439,794
HGNC
HGNC:43479 HGNC
Ensembl
ENSG00000263705 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Ranking
ClinVar
0
0
0
0
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
Search Word
Target data :
MGeND data only
Category :
Search word :
Filtering :
Variant name Gene AA change CDS Japanese
frequency		 TogoVar MGeND Genome ClinVar CIViC evidence DisGeNET entry COSMIC
occurrence		 Prediction
Entry Origin Type Annotation Entry Origin Annotation
Search Word
Target data :
MGeND data only
Category :
Search word :
Filtering :
Name MGeND Type Genome Size Chromosome Start Stop Ref Alt ClinVar Origin Entry CIViC evidence DisGeNET entry
Entry Origin Type Annotation
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
Entry Origin Type Annotation
TypeID
HGNC HGNC:43479 HGNC
Ensembl ENSG00000263705 Ensembl
miRBase MI0019294
AllianceGenome HGNC:43479
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000581998.1 hg38 chr6 10,439,717 10,439,794 78
ENST00000581998.1 hg19 chr6 10,439,950 10,440,027 78
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