LOC283387 uncharacterized LOC283387

Information
Symbol
LOC283387
Type
ncRNA
Description
uncharacterized LOC283387
Entrez Gene ID
283387
Genome
hg19
Position
chr12:58,263,618-58,290,265
Genome
hg38
Position
chr12:57,869,835-57,896,482
Ensembl
ENSG00000245651 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
Ensembl ENSG00000245651 Ensembl
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000499481.2 hg38 chr12 57,869,835 57,896,482 26,648
ENST00000664759.1 hg38 chr12 57,869,839 57,872,870 3,032
ENST00000664926.1 hg38 chr12 57,869,838 57,894,914 25,077
ENST00000667552.1 hg38 chr12 57,892,989 57,894,919 1,931
ENST00000499481.2 hg19 chr12 58,263,618 58,290,265 26,648
ENST00000664926.1 hg19 chr12 58,263,621 58,288,697 25,077
ENST00000664759.1 hg19 chr12 58,263,622 58,266,653 3,032
ENST00000667552.1 hg19 chr12 58,286,772 58,288,702 1,931
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