MIR4705 microRNA 4705

Information
Symbol
MIR4705
Type
ncRNA
Description
microRNA 4705
Entrez Gene ID
100616239
Genome
hg19
Position
chr13:102,698,284-102,698,354
Genome
hg38
Position
chr13:102,045,934-102,046,004
HGNC
HGNC:41567 HGNC
Ensembl
ENSG00000264482 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:41567 HGNC
Ensembl ENSG00000264482 Ensembl
miRBase MI0017338
AllianceGenome HGNC:41567
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000577547.1 hg38 chr13 102,045,934 102,046,004 71
ENST00000577547.1 hg19 chr13 102,698,284 102,698,354 71
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