MIR4715 microRNA 4715

Information
Symbol
MIR4715
Type
ncRNA
Description
microRNA 4715
Entrez Gene ID
100616474
Genome
hg19
Position
chr15:26,093,894-26,093,972
Genome
hg38
Position
chr15:25,848,747-25,848,825
HGNC
HGNC:41666 HGNC
Ensembl
ENSG00000266517 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
not provided 2 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:41666 HGNC
Ensembl ENSG00000266517 Ensembl
miRBase MI0017349
AllianceGenome HGNC:41666
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000584117.1 hg38 chr15 25,848,747 25,848,825 79
ENST00000584117.1 hg19 chr15 26,093,894 26,093,972 79
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