MIR6862-2 microRNA 6862-2

Information
Symbol
MIR6862-2
Type
ncRNA
Description
microRNA 6862-2
Entrez Gene ID
102465907
Genome
hg38
Position
chr16:28,724,252-28,724,321
HGNC
HGNC:50192 HGNC
Ensembl
ENSG00000278340 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
not provided 1 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-6862-2
HGNC HGNC:50192 HGNC
Ensembl ENSG00000278340 Ensembl
miRBase MI0026415
AllianceGenome HGNC:50192
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000614755.1 hg38 chr16 28,724,252 28,724,321 70
Genome browser