MIR5692C2 microRNA 5692c-2

Information
Symbol
MIR5692C2
Type
ncRNA
Description
microRNA 5692c-2
Entrez Gene ID
100847017
Genome
hg19
Position
chr7:97,593,717-97,593,793
Genome
hg38
Position
chr7:97,964,405-97,964,481
HGNC
HGNC:43448 HGNC
Ensembl
ENSG00000266668 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:43448 HGNC
Ensembl ENSG00000266668 Ensembl
miRBase MI0019289
AllianceGenome HGNC:43448
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000577959.1 hg38 chr7 97,964,405 97,964,481 77
ENST00000577959.1 hg19 chr7 97,593,717 97,593,793 77
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