ZNF594-DT ZNF594 divergent transcript

Information
Symbol
ZNF594-DT
Type
ncRNA
Description
ZNF594 divergent transcript
Entrez Gene ID
100130950
Genome
hg19
Position
chr17:5,095,363-5,138,900
Genome
hg38
Position
chr17:5,192,068-5,235,605
HGNC
HGNC:55347 HGNC
Ensembl
ENSG00000261879 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:55347 HGNC
Ensembl ENSG00000261879 Ensembl
AllianceGenome HGNC:55347
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000649359.1 hg38 chr17 5,192,090 5,235,637 43,548
ENST00000663434.1 hg38 chr17 5,192,068 5,235,605 43,538
ENST00000571689.1 hg38 chr17 5,192,104 5,235,643 43,540
ENST00000669386.1 hg38 chr17 5,192,027 5,235,995 43,969
ENST00000669386.1 hg19 chr17 5,095,322 5,139,290 43,969
ENST00000663434.1 hg19 chr17 5,095,363 5,138,900 43,538
ENST00000649359.1 hg19 chr17 5,095,385 5,138,932 43,548
ENST00000571689.1 hg19 chr17 5,095,399 5,138,938 43,540
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