MIR6862-1 microRNA 6862-1

Information
Symbol
MIR6862-1
Type
ncRNA
Description
microRNA 6862-1
Entrez Gene ID
102465520
Genome
hg38
Position
chr16:28,390,982-28,391,051
HGNC
HGNC:50052 HGNC
Ensembl
ENSG00000275429 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-6862-1
HGNC HGNC:50052 HGNC
Ensembl ENSG00000275429 Ensembl
miRBase MI0022709
AllianceGenome HGNC:50052
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000613016.1 hg38 chr16 28,390,982 28,391,051 70
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