MIR6787 microRNA 6787

Information
Symbol
MIR6787
Type
ncRNA
Description
microRNA 6787
Entrez Gene ID
102465472
Genome
hg38
Position
chr17:82,236,668-82,236,728
HGNC
HGNC:50209 HGNC
Ensembl
ENSG00000284574 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-6787
HGNC HGNC:50209 HGNC
Ensembl ENSG00000284574 Ensembl
miRBase MI0022632
AllianceGenome HGNC:50209
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000616675.1 hg38 chr17 82,236,668 82,236,728 61
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