LOC102723536 uncharacterized LOC102723536

Information
Symbol
LOC102723536
Type
ncRNA
Description
uncharacterized LOC102723536
Entrez Gene ID
102723536
Genome
hg19
Position
chr16:26,329,467-26,334,302
Genome
hg38
Position
chr16:26,318,146-26,322,981
Ensembl
ENSG00000231876 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 ENSG00000231876 Ensembl
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000452511.5 hg38 chr16 26,318,146 26,322,981 4,836
ENST00000669218.1 hg38 chr16 26,318,090 26,340,815 22,726
ENST00000662427.1 hg38 chr16 26,318,133 26,334,428 16,296
ENST00000653907.1 hg38 chr16 26,318,107 26,340,748 22,642
ENST00000669218.1 hg19 chr16 26,329,411 26,352,136 22,726
ENST00000653907.1 hg19 chr16 26,329,428 26,352,069 22,642
ENST00000662427.1 hg19 chr16 26,329,454 26,345,749 16,296
ENST00000452511.5 hg19 chr16 26,329,467 26,334,302 4,836
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