ZNF559 zinc finger protein 559
Information
- Symbol
- ZNF559
- Type
- protein-coding
- Description
- zinc finger protein 559
- Entrez Gene ID
- 84527
- Genome
- hg19
- Position
- chr19:9,434,448-9,454,519
- Genome
- hg38
- Position
- chr19:9,323,772-9,343,843
- HGNC
- HGNC:28197 HGNC
- Ensembl
- ENSG00000188321 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 2 |
Likely benign | 0 | 6 |
Uncertain significance | 0 | 96 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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0 |
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104 |
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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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Filtering | : |
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 |
Type | ID |
---|---|
SYNONYM | NBLA00121 |
HGNC | HGNC:28197 HGNC |
Ensembl | ENSG00000188321 Ensembl |
AllianceGenome | HGNC:28197 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000585352.5 | hg38 | chr19 | 9,324,179 | 9,342,148 | 17,970 |
ENST00000592896.5 | hg38 | chr19 | 9,324,197 | 9,342,465 | 18,269 |
ENST00000587557.5 | hg38 | chr19 | 9,323,772 | 9,343,843 | 20,072 |
ENST00000393883.6 | hg38 | chr19 | 9,324,252 | 9,345,898 | 21,647 |
ENST00000592504.5 | hg38 | chr19 | 9,324,179 | 9,342,084 | 17,906 |
ENST00000586255.5 | hg38 | chr19 | 9,324,179 | 9,351,162 | 26,984 |
ENST00000317221.11 | hg38 | chr19 | 9,324,179 | 9,343,843 | 19,665 |
ENST00000603380.6 | hg38 | chr19 | 9,324,179 | 9,345,871 | 21,693 |
ENST00000587557.5 | hg19 | chr19 | 9,434,448 | 9,454,519 | 20,072 |
ENST00000592504.5 | hg19 | chr19 | 9,434,855 | 9,452,760 | 17,906 |
ENST00000585352.5 | hg19 | chr19 | 9,434,855 | 9,452,824 | 17,970 |
ENST00000317221.11 | hg19 | chr19 | 9,434,855 | 9,454,519 | 19,665 |
ENST00000603380.6 | hg19 | chr19 | 9,434,855 | 9,456,547 | 21,693 |
ENST00000586255.5 | hg19 | chr19 | 9,434,855 | 9,461,838 | 26,984 |
ENST00000592896.5 | hg19 | chr19 | 9,434,873 | 9,453,141 | 18,269 |
ENST00000393883.6 | hg19 | chr19 | 9,434,928 | 9,456,574 | 21,647 |
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