ZNF559-ZNF177 ZNF559-ZNF177 readthrough

Information
Symbol
ZNF559-ZNF177
Type
protein-coding
Description
ZNF559-ZNF177 readthrough
Entrez Gene ID
100529215
Genome
hg19
Position
chr19:9,435,017-9,493,293
Genome
hg38
Position
chr19:9,324,341-9,382,617
HGNC
HGNC:42964 HGNC
Ensembl
ENSG00000270011 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 2
Likely benign 0 6
Uncertain significance 0 116
Ranking
ClinVar
0
0
0
124
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:42964 HGNC
Ensembl ENSG00000270011 Ensembl
AllianceGenome HGNC:42964
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000541595.6 hg38 chr19 9,324,341 9,382,617 58,277
ENST00000446085.8 hg38 chr19 9,324,174 9,382,190 58,017
ENST00000446085.8 hg19 chr19 9,434,850 9,492,866 58,017
ENST00000541595.6 hg19 chr19 9,435,017 9,493,293 58,277
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