LOC105369908 uncharacterized LOC105369908

Information
Symbol
LOC105369908
Type
ncRNA
Description
uncharacterized LOC105369908
Entrez Gene ID
105369908
Genome
hg19
Position
chr12:93,484,256-93,502,390
Genome
hg38
Position
chr12:93,090,480-93,108,614
Ensembl
ENSG00000257746 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 ENSG00000257746 Ensembl
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000551928.1 hg38 chr12 93,090,522 93,107,600 17,079
ENST00000665612.1 hg38 chr12 93,090,490 93,093,473 2,984
ENST00000657309.1 hg38 chr12 93,090,480 93,108,614 18,135
ENST00000660842.1 hg38 chr12 93,095,676 93,108,629 12,954
ENST00000657309.1 hg19 chr12 93,484,256 93,502,390 18,135
ENST00000665612.1 hg19 chr12 93,484,266 93,487,249 2,984
ENST00000551928.1 hg19 chr12 93,484,298 93,501,376 17,079
ENST00000660842.1 hg19 chr12 93,489,452 93,502,405 12,954
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