MIR3929 microRNA 3929

Information
Symbol
MIR3929
Type
ncRNA
Description
microRNA 3929
Entrez Gene ID
100500864
Genome
hg19
Position
chr18:33,514,051-33,514,105
Genome
hg38
Position
chr18:35,934,088-35,934,142
HGNC
HGNC:38945 HGNC
Ensembl
ENSG00000265641 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:38945 HGNC
Ensembl ENSG00000265641 Ensembl
miRBase MI0016439
AllianceGenome HGNC:38945
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000584497.1 hg38 chr18 35,934,088 35,934,142 55
ENST00000584497.1 hg19 chr18 33,514,051 33,514,105 55
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