MIR3928 microRNA 3928

Information
Symbol
MIR3928
Type
ncRNA
Description
microRNA 3928
Entrez Gene ID
100500901
Genome
hg19
Position
chr22:31,556,048-31,556,105
Genome
hg38
Position
chr22:31,160,062-31,160,119
HGNC
HGNC:38933 HGNC
Ensembl
ENSG00000264141 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
SYNONYM mir-3928
HGNC HGNC:38933 HGNC
Ensembl ENSG00000264141 Ensembl
miRBase MI0016438
AllianceGenome HGNC:38933
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000583386.1 hg38 chr22 31,160,062 31,160,119 58
ENST00000583386.1 hg19 chr22 31,556,048 31,556,105 58
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