LOC107984132 uncharacterized LOC107984132

Information
Symbol
LOC107984132
Type
ncRNA
Description
uncharacterized LOC107984132
Entrez Gene ID
107984132
Genome
hg19
Position
chr13:19,648,178-19,692,455
Genome
hg38
Position
chr13:19,074,038-19,118,315
Ensembl
ENSG00000287861 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 ENSG00000287861 Ensembl
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000657315.1 hg38 chr13 19,074,038 19,118,315 44,278
ENST00000657315.1 hg19 chr13 19,648,178 19,692,455 44,278
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