LOC105370670 uncharacterized LOC105370670

Information
Symbol
LOC105370670
Type
ncRNA
Description
uncharacterized LOC105370670
Entrez Gene ID
105370670
Genome
hg19
Position
chr14:101,538,315-101,544,008
Genome
hg38
Position
chr14:101,071,978-101,077,671
Ensembl
ENSG00000230805 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 ENSG00000230805 Ensembl
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000673125.1 hg38 chr14 101,071,978 101,077,675 5,698
ENST00000654748.1 hg38 chr14 101,073,718 101,077,660 3,943
ENST00000555103.1 hg38 chr14 101,073,953 101,077,910 3,958
ENST00000448840.7 hg38 chr14 101,071,978 101,077,671 5,694
ENST00000448840.7 hg19 chr14 101,538,315 101,544,008 5,694
ENST00000673125.1 hg19 chr14 101,538,315 101,544,012 5,698
ENST00000654748.1 hg19 chr14 101,540,055 101,543,997 3,943
ENST00000555103.1 hg19 chr14 101,540,290 101,544,247 3,958
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