MIR4799 microRNA 4799

Information
Symbol
MIR4799
Type
ncRNA
Description
microRNA 4799
Entrez Gene ID
100616246
Genome
hg19
Position
chr4:148,703,746-148,703,819
Genome
hg38
Position
chr4:147,782,595-147,782,668
HGNC
HGNC:41584 HGNC
Ensembl
ENSG00000264274 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:41584 HGNC
Ensembl ENSG00000264274 Ensembl
miRBase MI0017446
AllianceGenome HGNC:41584
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000578951.1 hg38 chr4 147,782,595 147,782,668 74
ENST00000578951.1 hg19 chr4 148,703,746 148,703,819 74
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