ZNF771 zinc finger protein 771
Information
- Symbol
- ZNF771
- Type
- protein-coding
- Description
- zinc finger protein 771
- Entrez Gene ID
- 51333
- Genome
- hg19
- Position
- chr16:30,418,927-30,430,735
- Genome
- hg38
- Position
- chr16:30,407,606-30,419,414
- HGNC
- HGNC:29653 HGNC
- Ensembl
- ENSG00000179965 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Likely benign | 0 | 2 |
| Uncertain significance | 0 | 48 |
Ranking
| ClinVar | |
|---|---|
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0 |
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0 |
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0 |
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50 |
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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 | |||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 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 | |||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 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 | |||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Entry | Origin | Type | Annotation | |||||||||||||||
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000319296.10 | hg38 | chr16 | 30,407,606 | 30,419,414 | 11,809 |
| ENST00000566625.2 | hg38 | chr16 | 30,407,629 | 30,431,108 | 23,480 |
| ENST00000564550.1 | hg38 | chr16 | 30,408,031 | 30,414,609 | 6,579 |
| ENST00000434417.1 | hg38 | chr16 | 30,407,414 | 30,418,594 | 11,181 |
| ENST00000434417.1 | hg19 | chr16 | 30,418,735 | 30,429,915 | 11,181 |
| ENST00000319296.10 | hg19 | chr16 | 30,418,927 | 30,430,735 | 11,809 |
| ENST00000566625.2 | hg19 | chr16 | 30,418,950 | 30,442,429 | 23,480 |
| ENST00000564550.1 | hg19 | chr16 | 30,419,352 | 30,425,930 | 6,579 |
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