LOC105377213 uncharacterized LOC105377213

Information
Symbol
LOC105377213
Type
ncRNA
Description
uncharacterized LOC105377213
Entrez Gene ID
105377213
Genome
hg19
Position
chrX:150,684,023-150,684,717
Genome
hg38
Position
chrX:151,515,551-151,516,245
Ensembl
ENSG00000214915 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 ENSG00000214915 Ensembl
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000454307.1 hg38 chrX 151,515,551 151,516,245 695
ENST00000454307.1 hg19 chrX 150,684,023 150,684,717 695
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