MIR3152 microRNA 3152

Information
Symbol
MIR3152
Type
ncRNA
Description
microRNA 3152
Entrez Gene ID
100422869
Genome
hg19
Position
chr9:18,573,304-18,573,377
Genome
hg38
Position
chr9:18,573,306-18,573,379
HGNC
HGNC:38379 HGNC
Ensembl
ENSG00000264638 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:38379 HGNC
Ensembl ENSG00000264638 Ensembl
miRBase MI0014179
AllianceGenome HGNC:38379
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000579801.1 hg38 chr9 18,573,306 18,573,379 74
ENST00000579801.1 hg19 chr9 18,573,304 18,573,377 74
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