MIR4766 microRNA 4766

Information
Symbol
MIR4766
Type
ncRNA
Description
microRNA 4766
Entrez Gene ID
100616283
Genome
hg19
Position
chr22:41,209,887-41,209,962
Genome
hg38
Position
chr22:40,813,883-40,813,958
HGNC
HGNC:41680 HGNC
Ensembl
ENSG00000266594 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
SYNONYM mir-4766
HGNC HGNC:41680 HGNC
Ensembl ENSG00000266594 Ensembl
miRBase MI0017407
AllianceGenome HGNC:41680
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000584704.1 hg38 chr22 40,813,883 40,813,958 76
ENST00000584704.1 hg19 chr22 41,209,887 41,209,962 76
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