LOC107985535 uncharacterized LOC107985535

Information
Symbol
LOC107985535
Type
ncRNA
Description
uncharacterized LOC107985535
Entrez Gene ID
107985535
Genome
hg19
Position
chr22:46,272,008-46,287,318
Genome
hg38
Position
chr22:45,876,128-45,891,438
Ensembl
ENSG00000235091 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
SYNONYM WI2-85898F10.1
Ensembl ENSG00000235091 Ensembl
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000650444.1 hg38 chr22 45,876,128 45,891,438 15,311
ENST00000650444.1 hg19 chr22 46,272,008 46,287,318 15,311
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