ZNF587 zinc finger protein 587
Information
- Symbol
- ZNF587
- Type
- protein-coding
- Description
- zinc finger protein 587
- Entrez Gene ID
- 84914
- Genome
- hg19
- Position
- chr19:58,361,227-58,376,485
- Genome
- hg38
- Position
- chr19:57,849,859-57,865,117
- HGNC
- HGNC:30955 HGNC
- Ensembl
- ENSG00000198466 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 10 |
Likely benign | 0 | 6 |
Uncertain significance | 0 | 54 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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0 |
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70 |
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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 |
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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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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 |
---|---|---|---|---|---|
ENST00000339656.8 | hg38 | chr19 | 57,849,859 | 57,865,117 | 15,259 |
ENST00000423137.1 | hg38 | chr19 | 57,849,860 | 57,860,210 | 10,351 |
ENST00000339656.8 | hg19 | chr19 | 58,361,227 | 58,376,485 | 15,259 |
ENST00000423137.1 | hg19 | chr19 | 58,361,228 | 58,371,578 | 10,351 |
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