MIR3978 microRNA 3978

Information
Symbol
MIR3978
Type
ncRNA
Description
microRNA 3978
Entrez Gene ID
100616491
Genome
hg19
Position
chrX:109,325,346-109,325,446
Genome
hg38
Position
chrX:110,082,118-110,082,218
HGNC
HGNC:41630 HGNC
Ensembl
ENSG00000265584 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
not provided 7 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:41630 HGNC
Ensembl ENSG00000265584 Ensembl
miRBase MI0016996
AllianceGenome HGNC:41630
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000585195.1 hg38 chrX 110,082,118 110,082,218 101
ENST00000585195.1 hg19 chrX 109,325,346 109,325,446 101
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