MIR3942 microRNA 3942

Information
Symbol
MIR3942
Type
ncRNA
Description
microRNA 3942
Entrez Gene ID
100500904
Genome
hg19
Position
chr15:35,664,457-35,664,565
Genome
hg38
Position
chr15:35,372,256-35,372,364
HGNC
HGNC:38976 HGNC
Ensembl
ENSG00000265102 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:38976 HGNC
Ensembl ENSG00000265102 Ensembl
miRBase MI0016599
AllianceGenome HGNC:38976
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000585264.1 hg38 chr15 35,372,256 35,372,364 109
ENST00000585264.1 hg19 chr15 35,664,457 35,664,565 109
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