MIR4762 microRNA 4762

Information
Symbol
MIR4762
Type
ncRNA
Description
microRNA 4762
Entrez Gene ID
100616253
Genome
hg19
Position
chr22:46,156,404-46,156,478
Genome
hg38
Position
chr22:45,760,524-45,760,598
HGNC
HGNC:41603 HGNC
Ensembl
ENSG00000264160 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
not provided 1 0
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
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:41603 HGNC
Ensembl ENSG00000264160 Ensembl
miRBase MI0017403
AllianceGenome HGNC:41603
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000585261.1 hg38 chr22 45,760,524 45,760,598 75
ENST00000585261.1 hg19 chr22 46,156,404 46,156,478 75
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