LOC105373289 LOC105373289

Information
Symbol
LOC105373289
Type
ncRNA
Description
LOC105373289
Entrez Gene ID
105373289
Genome
hg19
Position
chr1:227,976,224-227,979,880
Genome
hg38
Position
chr1:227,788,523-227,792,179
Ensembl
ENSG00000286389 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 ENSG00000286389 Ensembl
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000684869.1 hg38 chr1 227,788,521 227,790,575 2,055
ENST00000665412.1 hg38 chr1 227,788,523 227,792,179 3,657
ENST00000684869.1 hg19 chr1 227,976,222 227,978,276 2,055
ENST00000665412.1 hg19 chr1 227,976,224 227,979,880 3,657
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