LOC105375972 uncharacterized LOC105375972

Information
Symbol
LOC105375972
Type
ncRNA
Description
uncharacterized LOC105375972
Entrez Gene ID
105375972
Genome
hg19
Position
chr9:9,799,423-9,803,784
Genome
hg38
Position
chr9:9,799,423-9,803,784
Ensembl
ENSG00000230920 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 ENSG00000230920 Ensembl
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000449531.1 hg38 chr9 9,799,423 9,803,784 4,362
ENST00000449531.1 hg19 chr9 9,799,423 9,803,784 4,362
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