ENST00000668051.1 MIAT

Information
Transcript ID
ENST00000668051.1
Genome
hg38
Position
chr22:26,646,411-26,666,225
Strand
+
CDS length
0
Amino acid length
0
Gene symbol
MIAT
Gene type
ncRNA
Gene description
myocardial infarction associated transcript
Gene Entrez Gene ID
440823
Variants

Display target variant


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Target data :
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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Target data :
MGeND data only
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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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Target data :
MGeND data only
Category :
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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 26,646,411 26,646,959
2 26,660,699 26,660,816
3 26,663,316 26,663,398
4 26,665,531 26,666,225
Other genome
Genome Chromosome Start End Links
hg19 chr22 27,042,375 27,062,189 Link
CDS sequence
Amino sequence