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 | |
---|---|
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0 |
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0 |
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0 |
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124 |
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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
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Variant name | Gene | AA change | CDS | Japanese frequency |
TogoVar | MGeND | Genome | ClinVar | CIViC evidence | DisGeNET entry | COSMIC occurrence |
Prediction | |||||
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Entry | Origin | Type | Annotation | Entry | Origin | Annotation |
Search Word
Target data | : |
MGeND data only
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Name | MGeND | Type | Genome | Size | Chromosome | Start | Stop | Ref | Alt | ClinVar | Origin | Entry | CIViC evidence | DisGeNET entry | |||
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Entry | Origin | Type | Annotation |
Search Word
Target data | : |
MGeND data only
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Category | : |
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Name | MGeND | Type | Genome | Gene symbol | Chromosome | Genomic start | Genomic stop | Strand | Ref | Alt | ClinVar | Origin | Entry | CIViC evidence | DisGeNET entry | |||
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Entry | Origin | Type | Annotation |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
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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