LOC100996671 uncharacterized LOC100996671

Information
Symbol
LOC100996671
Type
ncRNA
Description
uncharacterized LOC100996671
Entrez Gene ID
100996671
Genome
hg19
Position
chr12:127,094,250-127,102,727
Genome
hg38
Position
chr12:126,609,704-126,618,181
Ensembl
ENSG00000256732 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 ENSG00000256732 Ensembl
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000689745.1 hg38 chr12 126,609,704 126,618,181 8,478
ENST00000541065.1 hg38 chr12 126,652,966 126,690,318 37,353
ENST00000689745.1 hg19 chr12 127,094,250 127,102,727 8,478
ENST00000541065.1 hg19 chr12 127,137,512 127,174,864 37,353
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