MIR4761 microRNA 4761

Information
Symbol
MIR4761
Type
ncRNA
Description
microRNA 4761
Entrez Gene ID
100616414
Genome
hg38
Position
chr22:19,963,753-19,963,834
HGNC
HGNC:41591 HGNC
Ensembl
ENSG00000284031 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
not provided 14 0
Ranking
ClinVar
0
0
0
0
0
Frequency
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
Disease area statistics
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:41591 HGNC
Ensembl ENSG00000284031 Ensembl
miRBase MI0017402
AllianceGenome HGNC:41591
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000585066.1 hg38 chr22 19,963,753 19,963,834 82
Genome browser