LOC105370027 uncharacterized LOC105370027

Information
Symbol
LOC105370027
Type
ncRNA
Description
uncharacterized LOC105370027
Entrez Gene ID
105370027
Genome
hg19
Position
chr12:119,825,796-120,032,306
Genome
hg38
Position
chr12:119,387,991-119,594,501
Ensembl
ENSG00000248636 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 ENSG00000248636 Ensembl
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000509470.2 hg38 chr12 119,387,991 119,594,501 206,511
ENST00000665601.1 hg38 chr12 119,361,247 119,594,242 232,996
ENST00000537366.5 hg38 chr12 119,387,987 119,668,079 280,093
ENST00000665601.1 hg19 chr12 119,799,052 120,032,047 232,996
ENST00000537366.5 hg19 chr12 119,825,792 120,105,884 280,093
ENST00000509470.2 hg19 chr12 119,825,796 120,032,306 206,511
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