MIR4682 microRNA 4682

Information
Symbol
MIR4682
Type
ncRNA
Description
microRNA 4682
Entrez Gene ID
100616322
Genome
hg19
Position
chr10:121,718,025-121,718,104
Genome
hg38
Position
chr10:119,958,513-119,958,592
HGNC
HGNC:41788 HGNC
Ensembl
ENSG00000265370 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:41788 HGNC
Ensembl ENSG00000265370 Ensembl
miRBase MI0017314
AllianceGenome HGNC:41788
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000580643.1 hg38 chr10 119,958,513 119,958,592 80
ENST00000580643.1 hg19 chr10 121,718,025 121,718,104 80
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