LOC105372990 uncharacterized LOC105372990

Information
Symbol
LOC105372990
Type
ncRNA
Description
uncharacterized LOC105372990
Entrez Gene ID
105372990
Genome
hg19
Position
chr22:30,828,673-30,832,053
Genome
hg38
Position
chr22:30,432,686-30,436,066
Ensembl
ENSG00000273428 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 ENSG00000273428 Ensembl
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000607893.2 hg38 chr22 30,432,686 30,436,066 3,381
ENST00000607893.2 hg19 chr22 30,828,673 30,832,053 3,381
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