MIR4462 microRNA 4462

Information
Symbol
MIR4462
Type
ncRNA
Description
microRNA 4462
Entrez Gene ID
100616413
Genome
hg19
Position
chr6:37,523,141-37,523,198
Genome
hg38
Position
chr6:37,555,365-37,555,422
HGNC
HGNC:41549 HGNC
Ensembl
ENSG00000263926 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:41549 HGNC
Ensembl ENSG00000263926 Ensembl
miRBase MI0016810
AllianceGenome HGNC:41549
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000579627.1 hg38 chr6 37,555,365 37,555,422 58
ENST00000579627.1 hg19 chr6 37,523,141 37,523,198 58
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