ENST00000550380.6 LNCOG

Information
Transcript ID
ENST00000550380.6
Genome
hg38
Position
chr12:76,259,883-76,305,969
Strand
+
CDS length
0
Amino acid length
0
Gene symbol
LNCOG
Gene type
ncRNA
Gene description
lncRNA osteogenesis associated
Gene Entrez Gene ID
105369848
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 76,259,883 76,259,981
2 76,292,116 76,292,270
3 76,293,813 76,294,005
4 76,304,474 76,305,969
Other genome
Genome Chromosome Start End Links
hg19 chr12 76,653,663 76,699,749 Link
CDS sequence
Amino sequence