MIR7977 microRNA 7977

Information
Symbol
MIR7977
Type
ncRNA
Description
microRNA 7977
Entrez Gene ID
102465858
Genome
hg38
Position
chr3:176,515,103-176,515,151
HGNC
HGNC:49969 HGNC
Ensembl
ENSG00000283333 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
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
SYNONYM hsa-mir-7977
HGNC HGNC:49969 HGNC
Ensembl ENSG00000283333 Ensembl
miRBase MI0025753
AllianceGenome HGNC:49969
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000636162.1 hg38 chr3 176,515,103 176,515,151 49
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