LOC105375448 uncharacterized LOC105375448

Information
Symbol
LOC105375448
Type
ncRNA
Description
uncharacterized LOC105375448
Entrez Gene ID
105375448
Genome
hg19
Position
chr7:108,238,823-108,245,246
Genome
hg38
Position
chr7:108,598,379-108,604,802
Ensembl
ENSG00000225647 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 ENSG00000225647 Ensembl
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000661717.1 hg38 chr7 108,598,379 108,604,802 6,424
ENST00000658357.1 hg38 chr7 108,605,759 108,614,193 8,435
ENST00000668672.1 hg38 chr7 108,598,352 108,639,349 40,998
ENST00000668672.1 hg19 chr7 108,238,796 108,279,793 40,998
ENST00000661717.1 hg19 chr7 108,238,823 108,245,246 6,424
ENST00000658357.1 hg19 chr7 108,246,203 108,254,637 8,435
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