MIR6797 microRNA 6797

Information
Symbol
MIR6797
Type
ncRNA
Description
microRNA 6797
Entrez Gene ID
102465478
Genome
hg38
Position
chr19:41,869,627-41,869,698
HGNC
HGNC:50169 HGNC
Ensembl
ENSG00000276926 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-6797
HGNC HGNC:50169 HGNC
Ensembl ENSG00000276926 Ensembl
miRBase MI0022642
AllianceGenome HGNC:50169
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000621706.1 hg38 chr19 41,869,627 41,869,698 72
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