ENST00000578142.1 MIR4666B

Information
Transcript ID
ENST00000578142.1
Genome
hg38
Position
chrX:29,574,278-29,574,358
Strand
+
CDS length
0
Amino acid length
0
Gene symbol
MIR4666B
Gene type
ncRNA
Gene description
microRNA 4666b
Gene Entrez Gene ID
100847047
Variants

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MGeND data only
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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
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Name MGeND Type Genome Size Chromosome Start Stop Ref Alt ClinVar Origin Entry CIViC evidence DisGeNET entry
Entry Origin Type Annotation
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MGeND data only
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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
Exon
Exon number Start Stop
1 29,574,278 29,574,358
Other genome
Genome Chromosome Start End Links
hg19 chrX 29,592,395 29,592,475 Link
CDS sequence
Amino sequence