LOC101928143 uncharacterized LOC101928143

Information
Symbol
LOC101928143
Type
ncRNA
Description
uncharacterized LOC101928143
Entrez Gene ID
101928143
Genome
hg19
Position
chr14:73,925,556-73,930,341
Genome
hg38
Position
chr14:73,458,850-73,463,635
Ensembl
ENSG00000284930 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 ENSG00000284930 Ensembl
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000557577.1 hg38 chr14 73,460,935 73,463,618 2,684
ENST00000647202.1 hg38 chr14 73,458,850 73,463,635 4,786
ENST00000643731.1 hg38 chr14 73,459,009 73,463,585 4,577
ENST00000647202.1 hg19 chr14 73,925,556 73,930,341 4,786
ENST00000643731.1 hg19 chr14 73,925,715 73,930,291 4,577
ENST00000557577.1 hg19 chr14 73,927,641 73,930,324 2,684
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