ZNF599 zinc finger protein 599
Information
- Symbol
- ZNF599
- Type
- protein-coding
- Description
- zinc finger protein 599
- Entrez Gene ID
- 148103
- Genome
- hg19
- Position
- chr19:35,248,978-35,264,120
- Genome
- hg38
- Position
- chr19:34,758,073-34,773,215
- HGNC
- HGNC:26408 HGNC
- Ensembl
- ENSG00000153896 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely benign | 0 | 10 |
Uncertain significance | 0 | 86 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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0 |
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96 |
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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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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 |
---|---|---|---|---|---|
ENST00000588760.1 | hg38 | chr19 | 34,766,968 | 34,773,200 | 6,233 |
ENST00000587354.6 | hg38 | chr19 | 34,762,795 | 34,773,229 | 10,435 |
ENST00000329285.13 | hg38 | chr19 | 34,758,073 | 34,773,215 | 15,143 |
ENST00000329285.13 | hg19 | chr19 | 35,248,978 | 35,264,120 | 15,143 |
ENST00000587354.6 | hg19 | chr19 | 35,253,700 | 35,264,134 | 10,435 |
ENST00000588760.1 | hg19 | chr19 | 35,257,873 | 35,264,105 | 6,233 |
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