LOC101927468 uncharacterized LOC101927468

Information
Symbol
LOC101927468
Type
ncRNA
Description
uncharacterized LOC101927468
Entrez Gene ID
101927468
Genome
hg19
Position
chr1:146,138,539-146,149,334
Genome
hg38
Position
chr1:148,208,528-148,222,222
Ensembl
ENSG00000227733 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 ENSG00000227733 Ensembl
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000599640.6 hg38 chr1 148,159,213 148,246,747 87,535
ENST00000628902.1 hg38 chr1 148,163,572 148,176,331 12,760
ENST00000661240.1 hg38 chr1 148,205,761 148,246,663 40,903
ENST00000664473.1 hg38 chr1 148,208,528 148,222,222 13,695
ENST00000660078.1 hg38 chr1 148,208,096 148,246,701 38,606
ENST00000596091.5 hg38 chr1 148,200,000 148,217,078 17,079
ENST00000496508.1 hg19 chr1 146,138,539 146,149,334 10,796
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