MIR6872 microRNA 6872

Information
Symbol
MIR6872
Type
ncRNA
Description
microRNA 6872
Entrez Gene ID
102465526
Genome
hg38
Position
chr3:50,273,236-50,273,297
HGNC
HGNC:50037 HGNC
Ensembl
ENSG00000283848 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-6872
HGNC HGNC:50037 HGNC
Ensembl ENSG00000283848 Ensembl
miRBase MI0022719
AllianceGenome HGNC:50037
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000612981.1 hg38 chr3 50,273,236 50,273,297 62
Genome browser