LOC101928627 uncharacterized LOC101928627

Information
Symbol
LOC101928627
Type
ncRNA
Description
uncharacterized LOC101928627
Entrez Gene ID
101928627
Genome
hg19
Position
chrX:36,383,741-36,458,375
Genome
hg38
Position
chrX:36,365,626-36,440,292
Ensembl
ENSG00000226484 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 ENSG00000226484 Ensembl
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000455438.2 hg38 chrX 36,365,626 36,440,292 74,667
ENST00000455438.2 hg19 chrX 36,383,741 36,458,375 74,635
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