ZNF787 zinc finger protein 787
Information
- Symbol
- ZNF787
- Type
- protein-coding
- Description
- zinc finger protein 787
- Entrez Gene ID
- 126208
- Genome
- hg19
- Position
- chr19:56,598,732-56,632,664
- Genome
- hg38
- Position
- chr19:56,087,366-56,121,295
- HGNC
- HGNC:26998 HGNC
- Ensembl
- ENSG00000142409 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely benign | 0 | 8 |
Uncertain significance | 0 | 52 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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0 |
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58 |
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2 |
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 |
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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 |
---|---|---|---|---|---|
ENST00000610935.2 | hg38 | chr19 | 56,087,366 | 56,121,295 | 33,930 |
ENST00000587279.1 | hg38 | chr19 | 56,101,650 | 56,121,250 | 19,601 |
ENST00000610935.2 | hg19 | chr19 | 56,598,732 | 56,632,664 | 33,933 |
ENST00000587279.1 | hg19 | chr19 | 56,613,019 | 56,632,619 | 19,601 |
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