LOC349160 uncharacterized LOC349160

Information
Symbol
LOC349160
Type
ncRNA
Description
uncharacterized LOC349160
Entrez Gene ID
349160
Genome
hg19
Position
chr7:136,468,822-136,866,518
Genome
hg38
Position
chr7:136,784,075-137,181,771
Ensembl
ENSG00000234352 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 ENSG00000234352 Ensembl
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000425981.2 hg38 chr7 136,898,773 137,164,341 265,569
ENST00000592183.5 hg38 chr7 136,785,832 137,182,107 396,276
ENST00000439694.5 hg38 chr7 136,784,075 137,181,771 397,697
ENST00000439694.5 hg19 chr7 136,468,822 136,866,518 397,697
ENST00000592183.5 hg19 chr7 136,470,579 136,866,854 396,276
ENST00000425981.2 hg19 chr7 136,583,520 136,849,088 265,569
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