LOC102724637 uncharacterized LOC102724637

Information
Symbol
LOC102724637
Type
ncRNA
Description
uncharacterized LOC102724637
Entrez Gene ID
102724637
Genome
hg19
Position
chr5:89,259,657-89,269,791
Genome
hg38
Position
chr5:89,963,840-89,973,974
Ensembl
ENSG00000214942 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 ENSG00000214942 Ensembl
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000505109.2 hg38 chr5 89,900,664 89,990,883 90,220
ENST00000652458.1 hg38 chr5 89,902,292 89,971,941 69,650
ENST00000666691.1 hg38 chr5 89,963,840 89,973,974 10,135
ENST00000505109.2 hg19 chr5 89,196,481 89,286,700 90,220
ENST00000652458.1 hg19 chr5 89,198,109 89,267,758 69,650
ENST00000666691.1 hg19 chr5 89,259,657 89,269,791 10,135
Genome browser