MIR6887 microRNA 6887

Information
Symbol
MIR6887
Type
ncRNA
Description
microRNA 6887
Entrez Gene ID
102466205
Genome
hg38
Position
chr19:35,122,700-35,122,764
HGNC
HGNC:50065 HGNC
Ensembl
ENSG00000284065 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
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 hsa-mir-6887
HGNC HGNC:50065 HGNC
Ensembl ENSG00000284065 Ensembl
miRBase MI0022734
AllianceGenome HGNC:50065
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000622822.1 hg38 chr19 35,122,700 35,122,764 65
Genome browser