LOC101928557 uncharacterized LOC101928557

Information
Symbol
LOC101928557
Type
ncRNA
Description
uncharacterized LOC101928557
Entrez Gene ID
101928557
Genome
hg19
Position
chr16:85,826,021-85,826,539
Genome
hg38
Position
chr16:85,792,415-85,792,933
Ensembl
ENSG00000270159 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 ENSG00000270159 Ensembl
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000602617.1 hg38 chr16 85,792,415 85,792,933 519
ENST00000602617.1 hg19 chr16 85,826,021 85,826,539 519
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