SYS1-DBNDD2 SYS1-DBNDD2 readthrough (NMD candidate)

Information
Symbol
SYS1-DBNDD2
Type
ncRNA
Description
SYS1-DBNDD2 readthrough (NMD candidate)
Entrez Gene ID
767557
Genome
hg19
Position
chr20:43,992,142-44,038,637
Genome
hg38
Position
chr20:45,363,502-45,409,997
HGNC
HGNC:33535 HGNC
Ensembl
ENSG00000254806 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
not provided 1 0
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
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
SYNONYM C20orf169-DBNDD2
HGNC HGNC:33535 HGNC
Ensembl ENSG00000254806 Ensembl
AllianceGenome HGNC:33535
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000458187.5 hg38 chr20 45,363,502 45,409,997 46,496
ENST00000458187.5 hg19 chr20 43,992,142 44,038,637 46,496
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