MIR4699 microRNA 4699

Information
Symbol
MIR4699
Type
ncRNA
Description
microRNA 4699
Entrez Gene ID
100616133
Genome
hg19
Position
chr12:81,552,167-81,552,240
Genome
hg38
Position
chr12:81,158,388-81,158,461
HGNC
HGNC:41636 HGNC
Ensembl
ENSG00000265227 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:41636 HGNC
Ensembl ENSG00000265227 Ensembl
miRBase MI0017332
AllianceGenome HGNC:41636
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000578957.1 hg38 chr12 81,158,388 81,158,461 74
ENST00000578957.1 hg19 chr12 81,552,167 81,552,240 74
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