MIR1279 microRNA 1279

Information
Symbol
MIR1279
Type
ncRNA
Description
microRNA 1279
Entrez Gene ID
100302182
Genome
hg38
Position
chr12:69,273,157-69,273,218
HGNC
HGNC:35357 HGNC
Ensembl
ENSG00000283476 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 MIRN1279
SYNONYM hsa-mir-1279
HGNC HGNC:35357 HGNC
Ensembl ENSG00000283476 Ensembl
miRBase MI0006426
AllianceGenome HGNC:35357
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000636976.1 hg38 chr12 69,273,157 69,273,218 62
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