MIR4494 microRNA 4494

Information
Symbol
MIR4494
Type
ncRNA
Description
microRNA 4494
Entrez Gene ID
100616478
Genome
hg19
Position
chr12:47,757,969-47,758,052
Genome
hg38
Position
chr12:47,364,186-47,364,269
HGNC
HGNC:41731 HGNC
Ensembl
ENSG00000264906 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:41731 HGNC
Ensembl ENSG00000264906 Ensembl
miRBase MI0016856
AllianceGenome HGNC:41731
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000577654.1 hg38 chr12 47,364,186 47,364,269 84
ENST00000577654.1 hg19 chr12 47,757,969 47,758,052 84
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