MIR4657 microRNA 4657

Information
Symbol
MIR4657
Type
ncRNA
Description
microRNA 4657
Entrez Gene ID
100616393
Genome
hg38
Position
chr7:44,881,748-44,881,800
HGNC
HGNC:41706 HGNC
Ensembl
ENSG00000284261 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
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-4657
HGNC HGNC:41706 HGNC
Ensembl ENSG00000284261 Ensembl
miRBase MI0017285
AllianceGenome HGNC:41706
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000578157.1 hg38 chr7 44,881,748 44,881,800 53
Genome browser