MIR4797 microRNA 4797

Information
Symbol
MIR4797
Type
ncRNA
Description
microRNA 4797
Entrez Gene ID
100616216
Genome
hg19
Position
chr3:197,020,749-197,020,819
Genome
hg38
Position
chr3:197,293,878-197,293,948
HGNC
HGNC:41758 HGNC
Ensembl
ENSG00000265850 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
not provided 4 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:41758 HGNC
Ensembl ENSG00000265850 Ensembl
miRBase MI0017444
AllianceGenome HGNC:41758
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000577559.1 hg38 chr3 197,293,878 197,293,948 71
ENST00000577559.1 hg19 chr3 197,020,749 197,020,819 71
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