MIR5687 microRNA 5687

Information
Symbol
MIR5687
Type
ncRNA
Description
microRNA 5687
Entrez Gene ID
100847019
Genome
hg19
Position
chr5:54,804,678-54,804,754
Genome
hg38
Position
chr5:55,508,850-55,508,926
HGNC
HGNC:43457 HGNC
Ensembl
ENSG00000265135 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:43457 HGNC
Ensembl ENSG00000265135 Ensembl
miRBase MI0019291
AllianceGenome HGNC:43457
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000581367.1 hg38 chr5 55,508,850 55,508,926 77
ENST00000581367.1 hg19 chr5 54,804,678 54,804,754 77
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