LOC100130357 uncharacterized LOC100130357

Information
Symbol
LOC100130357
Type
ncRNA
Description
uncharacterized LOC100130357
Entrez Gene ID
100130357
Genome
hg19
Position
chr6:13,279,527-13,295,818
Genome
hg38
Position
chr6:13,279,295-13,295,586
Ensembl
ENSG00000215022 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 ENSG00000215022 Ensembl
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000606150.5 hg38 chr6 13,279,295 13,295,586 16,292
ENST00000606627.1 hg38 chr6 13,264,861 13,274,059 9,199
ENST00000606627.1 hg19 chr6 13,265,093 13,274,291 9,199
ENST00000606150.5 hg19 chr6 13,279,527 13,295,818 16,292
Genome browser