MIR3914-1 microRNA 3914-1

Information
Symbol
MIR3914-1
Type
ncRNA
Description
microRNA 3914-1
Entrez Gene ID
100500836
Genome
hg19
Position
chr7:70,772,658-70,772,742
Genome
hg38
Position
chr7:71,307,672-71,307,770
HGNC
HGNC:38993 HGNC
Ensembl
ENSG00000265878 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:38993 HGNC
Ensembl ENSG00000265878 Ensembl
miRBase MI0016419
AllianceGenome HGNC:38993
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000584357.2 hg38 chr7 71,307,672 71,307,770 99
ENST00000584357.1 hg19 chr7 70,772,658 70,772,742 85
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