LOC100506790 uncharacterized LOC100506790

Information
Symbol
LOC100506790
Type
ncRNA
Description
uncharacterized LOC100506790
Entrez Gene ID
100506790
Genome
hg19
Position
chrX:134,530,354-134,531,689
Genome
hg38
Position
chrX:135,396,429-135,397,764
Ensembl
ENSG00000290806 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 ENSG00000290806 Ensembl
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000439434.1 hg38 chrX 135,396,429 135,397,764 1,336
ENST00000439434.1 hg19 chrX 134,530,354 134,531,689 1,336
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