MIR4708 microRNA 4708

Information
Symbol
MIR4708
Type
ncRNA
Description
microRNA 4708
Entrez Gene ID
100616176
Genome
hg19
Position
chr14:65,801,835-65,801,901
Genome
hg38
Position
chr14:65,335,117-65,335,183
HGNC
HGNC:41824 HGNC
Ensembl
ENSG00000266740 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-4708
HGNC HGNC:41824 HGNC
Ensembl ENSG00000266740 Ensembl
miRBase MI0017341
AllianceGenome HGNC:41824
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000584635.1 hg38 chr14 65,335,117 65,335,183 67
ENST00000584635.1 hg19 chr14 65,801,835 65,801,901 67
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