MIR592 microRNA 592

Information
Symbol
MIR592
Type
ncRNA
Description
microRNA 592
Entrez Gene ID
693177
Genome
hg19
Position
chr7:126,698,142-126,698,238
Genome
hg38
Position
chr7:127,058,088-127,058,184
HGNC
HGNC:32848 HGNC
Ensembl
ENSG00000207692 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 MIRN592
SYNONYM hsa-mir-592
SYNONYM mir-592
HGNC HGNC:32848 HGNC
Ensembl ENSG00000207692 Ensembl
miRBase MI0003604
AllianceGenome HGNC:32848
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000384959.3 hg38 chr7 127,058,088 127,058,184 97
ENST00000384959.1 hg19 chr7 126,698,142 126,698,238 97
Genome browser