MIR4698 microRNA 4698

Information
Symbol
MIR4698
Type
ncRNA
Description
microRNA 4698
Entrez Gene ID
100616486
Genome
hg19
Position
chr12:47,581,595-47,581,674
Genome
hg38
Position
chr12:47,187,812-47,187,891
HGNC
HGNC:41867 HGNC
Ensembl
ENSG00000263838 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:41867 HGNC
Ensembl ENSG00000263838 Ensembl
miRBase MI0017331
AllianceGenome HGNC:41867
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000577795.1 hg38 chr12 47,187,812 47,187,891 80
ENST00000577795.1 hg19 chr12 47,581,595 47,581,674 80
Genome browser