LOC100288728 uncharacterized LOC100288728

Information
Symbol
LOC100288728
Type
ncRNA
Description
uncharacterized LOC100288728
Entrez Gene ID
100288728
Genome
hg19
Position
chr17:3,038,263-3,080,229
Genome
hg38
Position
chr17:3,134,969-3,176,935
Ensembl
ENSG00000261848 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 ENSG00000261848 Ensembl
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000572821.5 hg38 chr17 3,134,969 3,176,935 41,967
ENST00000575487.1 hg38 chr17 3,163,005 3,177,031 14,027
ENST00000572821.5 hg19 chr17 3,038,263 3,080,229 41,967
ENST00000575487.1 hg19 chr17 3,066,299 3,080,325 14,027
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