ENST00000669469.1 LOC101927769

Information
Transcript ID
ENST00000669469.1
Genome
hg38
Position
chr7:20,296,687-20,314,483
Strand
+
CDS length
0
Amino acid length
0
Gene symbol
LOC101927769
Gene type
ncRNA
Gene description
uncharacterized LOC101927769
Gene Entrez Gene ID
101927769
Variants

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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
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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 20,296,687 20,296,759
2 20,298,282 20,298,466
3 20,301,012 20,301,057
4 20,305,792 20,306,023
5 20,311,035 20,311,154
6 20,313,636 20,313,743
7 20,314,240 20,314,483
Other genome
Genome Chromosome Start End Links
hg19 chr7 20,336,310 20,354,106 Link
CDS sequence
Amino sequence