LOC100507250 uncharacterized LOC100507250

Information
Symbol
LOC100507250
Type
ncRNA
Description
uncharacterized LOC100507250
Entrez Gene ID
100507250
Genome
hg19
Position
chr12:69,068,151-69,080,639
Genome
hg38
Position
chr12:68,674,371-68,686,859
Ensembl
ENSG00000247363 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 ENSG00000247363 Ensembl
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000502102.2 hg38 chr12 68,675,350 68,687,755 12,406
ENST00000500695.2 hg38 chr12 68,674,371 68,686,859 12,489
ENST00000690517.1 hg38 chr12 68,674,510 68,686,876 12,367
ENST00000500695.2 hg19 chr12 69,068,151 69,080,639 12,489
ENST00000690517.1 hg19 chr12 69,068,290 69,080,656 12,367
ENST00000502102.2 hg19 chr12 69,069,130 69,081,535 12,406
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