MIR6857 microRNA 6857

Information
Symbol
MIR6857
Type
ncRNA
Description
microRNA 6857
Entrez Gene ID
102465516
Genome
hg38
Position
chrX:53,405,673-53,405,765
HGNC
HGNC:50263 HGNC
Ensembl
ENSG00000278204 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
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 hsa-mir-6857
HGNC HGNC:50263 HGNC
Ensembl ENSG00000278204 Ensembl
miRBase MI0022703
AllianceGenome HGNC:50263
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000613267.1 hg38 chrX 53,405,673 53,405,765 93
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