LOC100507547 uncharacterized LOC100507547

Information
Symbol
LOC100507547
Type
ncRNA
Description
uncharacterized LOC100507547
Entrez Gene ID
100507547
Genome
hg19
Position
chr6:32,120,579-32,122,110
Genome
hg38
Position
chr6:32,152,802-32,154,333
Ensembl
ENSG00000284954 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 ENSG00000284954 Ensembl
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000485392.5 hg38 chr6 32,152,802 32,154,333 1,532
ENST00000475826.1 hg38 chr6 32,153,385 32,154,326 942
ENST00000485392.5 hg19 chr6 32,120,579 32,122,110 1,532
ENST00000475826.1 hg19 chr6 32,121,162 32,122,103 942
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