LOC105372971 uncharacterized LOC105372971

Information
Symbol
LOC105372971
Type
ncRNA
Description
uncharacterized LOC105372971
Entrez Gene ID
105372971
Genome
hg19
Position
chr22:26,557,871-26,564,719
Genome
hg38
Position
chr22:26,161,905-26,168,753
Ensembl
ENSG00000229770 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 ENSG00000229770 Ensembl
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000652418.1 hg38 chr22 26,161,905 26,168,753 6,849
ENST00000434510.2 hg38 chr22 26,161,912 26,169,341 7,430
ENST00000652418.1 hg19 chr22 26,557,871 26,564,719 6,849
ENST00000434510.2 hg19 chr22 26,557,878 26,565,307 7,430
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