MIR500B microRNA 500b

Information
Symbol
MIR500B
Type
ncRNA
Description
microRNA 500b
Entrez Gene ID
100422911
Genome
hg19
Position
chrX:49,775,279-49,775,357
Genome
hg38
Position
chrX:50,010,672-50,010,750
HGNC
HGNC:38223 HGNC
Ensembl
ENSG00000239057 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
not provided 6 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
SYNONYM mir-500b
HGNC HGNC:38223 HGNC
Ensembl ENSG00000239057 Ensembl
miRBase MI0015903
AllianceGenome HGNC:38223
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000458843.2 hg38 chrX 50,010,672 50,010,750 79
ENST00000458843.1 hg19 chrX 49,775,279 49,775,357 79
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