MIR3667 microRNA 3667

Information
Symbol
MIR3667
Type
ncRNA
Description
microRNA 3667
Entrez Gene ID
100500882
Genome
hg19
Position
chr22:49,937,041-49,937,114
Genome
hg38
Position
chr22:49,543,393-49,543,466
HGNC
HGNC:38990 HGNC
Ensembl
ENSG00000264139 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
not provided 1 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:38990 HGNC
Ensembl ENSG00000264139 Ensembl
miRBase MI0016068
AllianceGenome HGNC:38990
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000581025.1 hg38 chr22 49,543,393 49,543,466 74
ENST00000581025.1 hg19 chr22 49,937,041 49,937,114 74
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