MIR513C microRNA 513c

Information
Symbol
MIR513C
Type
ncRNA
Description
microRNA 513c
Entrez Gene ID
100302114
Genome
hg19
Position
chrX:146,271,222-146,271,305
Genome
hg38
Position
chrX:147,189,704-147,189,787
HGNC
HGNC:33934 HGNC
Ensembl
ENSG00000216171 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
not provided 6 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
SYNONYM MIRN513C
SYNONYM hsa-mir-513c
HGNC HGNC:33934 HGNC
Ensembl ENSG00000216171 Ensembl
miRBase MI0006649
AllianceGenome HGNC:33934
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000401352.1 hg38 chrX 147,189,704 147,189,787 84
ENST00000401352.1 hg19 chrX 146,271,222 146,271,305 84
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