MIR5684 microRNA 5684

Information
Symbol
MIR5684
Type
ncRNA
Description
microRNA 5684
Entrez Gene ID
100847071
Genome
hg19
Position
chr19:12,897,942-12,898,006
Genome
hg38
Position
chr19:12,787,128-12,787,192
HGNC
HGNC:43544 HGNC
Ensembl
ENSG00000263800 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:43544 HGNC
Ensembl ENSG00000263800 Ensembl
miRBase MI0019285
AllianceGenome HGNC:43544
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000585074.1 hg38 chr19 12,787,128 12,787,192 65
ENST00000585074.1 hg19 chr19 12,897,942 12,898,006 65
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