NQO2-AS1 NQO2 antisense RNA 1

Information
Symbol
NQO2-AS1
Type
ncRNA
Description
NQO2 antisense RNA 1
Entrez Gene ID
105374888
Genome
hg19
Position
chr6:2,989,570-2,999,838
Genome
hg38
Position
chr6:2,989,336-2,999,604
HGNC
HGNC:40407 HGNC
Ensembl
ENSG00000224846 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
HGNC HGNC:40407 HGNC
Ensembl ENSG00000224846 Ensembl
AllianceGenome HGNC:40407
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000660868.1 hg38 chr6 2,989,336 2,999,604 10,269
ENST00000665347.1 hg38 chr6 2,989,726 2,999,177 9,452
ENST00000660868.1 hg19 chr6 2,989,570 2,999,838 10,269
ENST00000665347.1 hg19 chr6 2,989,960 2,999,411 9,452
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