LOC100506606 uncharacterized LOC100506606

Information
Symbol
LOC100506606
Type
ncRNA
Description
uncharacterized LOC100506606
Entrez Gene ID
100506606
Genome
hg19
Position
chr12:29,430,888-29,436,184
Genome
hg38
Position
chr12:29,277,955-29,283,251
Ensembl
ENSG00000257176 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 ENSG00000257176 Ensembl
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000553105.1 hg38 chr12 29,280,418 29,317,848 37,431
ENST00000655500.1 hg38 chr12 29,277,955 29,283,251 5,297
ENST00000655500.1 hg19 chr12 29,430,888 29,436,184 5,297
ENST00000553105.1 hg19 chr12 29,433,351 29,470,781 37,431
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