LOC645485 uncharacterized LOC645485

Information
Symbol
LOC645485
Type
ncRNA
Description
uncharacterized LOC645485
Entrez Gene ID
645485
Genome
hg19
Position
chr12:30,948,745-30,970,369
Genome
hg38
Position
chr12:30,795,811-30,817,435
Ensembl
ENSG00000285517 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 ENSG00000285517 Ensembl
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000648367.1 hg38 chr12 30,795,721 30,802,795 7,075
ENST00000649354.1 hg38 chr12 30,795,948 30,803,176 7,229
ENST00000648050.1 hg38 chr12 30,795,811 30,817,435 21,625
ENST00000648700.1 hg38 chr12 30,796,077 30,879,268 83,192
ENST00000648367.1 hg19 chr12 30,948,655 30,955,729 7,075
ENST00000648050.1 hg19 chr12 30,948,745 30,970,369 21,625
ENST00000649354.1 hg19 chr12 30,948,882 30,956,110 7,229
ENST00000648700.1 hg19 chr12 30,949,011 31,032,202 83,192
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