LOC100131496 uncharacterized LOC100131496

Information
Symbol
LOC100131496
Type
ncRNA
Description
uncharacterized LOC100131496
Entrez Gene ID
100131496
Genome
hg19
Position
chr20:45,947,246-45,949,498
Genome
hg38
Position
chr20:47,318,502-47,320,754
Ensembl
ENSG00000267882 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 ENSG00000267882 Ensembl
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000599904.2 hg38 chr20 47,318,502 47,320,754 2,253
ENST00000599904.2 hg19 chr20 45,947,246 45,949,498 2,253
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