MIR4714 microRNA 4714

Information
Symbol
MIR4714
Type
ncRNA
Description
microRNA 4714
Entrez Gene ID
100616432
Genome
hg19
Position
chr15:99,327,655-99,327,731
Genome
hg38
Position
chr15:98,784,426-98,784,502
HGNC
HGNC:41763 HGNC
Ensembl
ENSG00000264480 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
not provided 3 0
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
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:41763 HGNC
Ensembl ENSG00000264480 Ensembl
miRBase MI0017348
AllianceGenome HGNC:41763
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000580728.1 hg38 chr15 98,784,426 98,784,502 77
ENST00000580728.1 hg19 chr15 99,327,655 99,327,731 77
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