MIR1247 microRNA 1247

Information
Symbol
MIR1247
Type
ncRNA
Description
microRNA 1247
Entrez Gene ID
100302145
Genome
hg38
Position
chr14:101,560,287-101,560,422
HGNC
HGNC:35313 HGNC
Ensembl
ENSG00000283857 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 MIRN1247
SYNONYM hsa-mir-1247
SYNONYM mir-1247
HGNC HGNC:35313 HGNC
Ensembl ENSG00000283857 Ensembl
miRBase MI0006382
AllianceGenome HGNC:35313
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000408206.1 hg38 chr14 101,560,287 101,560,422 136
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