LOC105370473 uncharacterized LOC105370473

Information
Symbol
LOC105370473
Type
ncRNA
Description
uncharacterized LOC105370473
Entrez Gene ID
105370473
Genome
hg19
Position
chr14:44,976,588-45,036,670
Genome
hg38
Position
chr14:44,507,385-44,567,467
Ensembl
ENSG00000258747 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 ENSG00000258747 Ensembl
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000662197.1 hg38 chr14 44,507,385 44,567,467 60,083
ENST00000557465.1 hg38 chr14 44,507,407 44,509,483 2,077
ENST00000556228.1 hg38 chr14 44,509,003 44,538,511 29,509
ENST00000662197.1 hg19 chr14 44,976,588 45,036,670 60,083
ENST00000557465.1 hg19 chr14 44,976,610 44,978,686 2,077
ENST00000556228.1 hg19 chr14 44,978,206 45,007,714 29,509
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