MIR4730 microRNA 4730

Information
Symbol
MIR4730
Type
ncRNA
Description
microRNA 4730
Entrez Gene ID
100616359
Genome
hg19
Position
chr17:78,393,218-78,393,293
Genome
hg38
Position
chr17:80,419,418-80,419,493
HGNC
HGNC:41880 HGNC
Ensembl
ENSG00000264961 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:41880 HGNC
Ensembl ENSG00000264961 Ensembl
miRBase MI0017367
AllianceGenome HGNC:41880
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000584535.1 hg38 chr17 80,419,418 80,419,493 76
ENST00000584535.1 hg19 chr17 78,393,218 78,393,293 76
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