MIR5696 microRNA 5696

Information
Symbol
MIR5696
Type
ncRNA
Description
microRNA 5696
Entrez Gene ID
100847007
Genome
hg19
Position
chr2:101,925,912-101,925,996
Genome
hg38
Position
chr2:101,309,450-101,309,534
HGNC
HGNC:43516 HGNC
Ensembl
ENSG00000264857 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:43516 HGNC
Ensembl ENSG00000264857 Ensembl
miRBase MI0019303
AllianceGenome HGNC:43516
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000578474.1 hg38 chr2 101,309,450 101,309,534 85
ENST00000578474.1 hg19 chr2 101,925,912 101,925,996 85
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