ZNF790-AS1 ZNF790 antisense RNA 1

Information
Symbol
ZNF790-AS1
Type
ncRNA
Description
ZNF790 antisense RNA 1
Entrez Gene ID
284408
Genome
hg19
Position
chr19:37,288,404-37,321,169
Genome
hg38
Position
chr19:36,797,502-36,830,267
HGNC
HGNC:27617 HGNC
Ensembl
ENSG00000267254 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:27617 HGNC
Ensembl ENSG00000267254 Ensembl
AllianceGenome HGNC:27617
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000587278.1 hg38 chr19 36,801,209 36,828,115 26,907
ENST00000655476.1 hg38 chr19 36,797,525 36,804,507 6,983
ENST00000702929.1 hg38 chr19 36,797,505 36,828,094 30,590
ENST00000657461.1 hg38 chr19 36,797,502 36,830,267 32,766
ENST00000650959.1 hg38 chr19 36,797,516 36,831,596 34,081
ENST00000657461.1 hg19 chr19 37,288,404 37,321,169 32,766
ENST00000702929.1 hg19 chr19 37,288,407 37,318,996 30,590
ENST00000650959.1 hg19 chr19 37,288,418 37,322,498 34,081
ENST00000655476.1 hg19 chr19 37,288,427 37,295,409 6,983
ENST00000587278.1 hg19 chr19 37,292,111 37,319,017 26,907
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