MIR3927 microRNA 3927

Information
Symbol
MIR3927
Type
ncRNA
Description
microRNA 3927
Entrez Gene ID
100500898
Genome
hg19
Position
chr9:112,273,755-112,273,825
Genome
hg38
Position
chr9:109,511,475-109,511,545
HGNC
HGNC:38901 HGNC
Ensembl
ENSG00000263861 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely pathogenic 1 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:38901 HGNC
Ensembl ENSG00000263861 Ensembl
miRBase MI0016435
AllianceGenome HGNC:38901
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000579313.1 hg38 chr9 109,511,475 109,511,545 71
ENST00000579313.1 hg19 chr9 112,273,755 112,273,825 71
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