LOC105369850 uncharacterized LOC105369850

Information
Symbol
LOC105369850
Type
ncRNA
Description
uncharacterized LOC105369850
Entrez Gene ID
105369850
Genome
hg19
Position
chr12:76,953,650-77,009,211
Genome
hg38
Position
chr12:76,559,870-76,615,431
Ensembl
ENSG00000257526 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 ENSG00000257526 Ensembl
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000702157.1 hg38 chr12 76,559,870 76,615,431 55,562
ENST00000702157.1 hg19 chr12 76,953,650 77,009,211 55,562
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