MIR4717 microRNA 4717

Information
Symbol
MIR4717
Type
ncRNA
Description
microRNA 4717
Entrez Gene ID
100616241
Genome
hg19
Position
chr16:2,324,621-2,324,692
Genome
hg38
Position
chr16:2,274,620-2,274,691
HGNC
HGNC:41571 HGNC
Ensembl
ENSG00000264004 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
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
HGNC HGNC:41571 HGNC
Ensembl ENSG00000264004 Ensembl
miRBase MI0017352
AllianceGenome HGNC:41571
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000584656.1 hg38 chr16 2,274,620 2,274,691 72
ENST00000584656.1 hg19 chr16 2,324,621 2,324,692 72
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