MIR449C microRNA 449c

Information
Symbol
MIR449C
Type
ncRNA
Description
microRNA 449c
Entrez Gene ID
100313923
Genome
hg19
Position
chr5:54,468,090-54,468,181
Genome
hg38
Position
chr5:55,172,262-55,172,353
HGNC
HGNC:37302 HGNC
Ensembl
ENSG00000251856 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
SYNONYM mir-449c
HGNC HGNC:37302 HGNC
Ensembl ENSG00000251856 Ensembl
miRBase MI0003823
AllianceGenome HGNC:37302
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000516047.1 hg38 chr5 55,172,262 55,172,353 92
ENST00000516047.1 hg19 chr5 54,468,090 54,468,181 92
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