LOC100652999 uncharacterized LOC100652999

Information
Symbol
LOC100652999
Type
ncRNA
Description
uncharacterized LOC100652999
Entrez Gene ID
100652999
Genome
hg19
Position
chr12:53,907,675-53,911,392
Genome
hg38
Position
chr12:53,513,891-53,517,608
Ensembl
ENSG00000257550 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 ENSG00000257550 Ensembl
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000548347.2 hg38 chr12 53,513,891 53,517,608 3,718
ENST00000548347.2 hg19 chr12 53,907,675 53,911,392 3,718
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