Variant Details for ZNF280B
Basic Information Top
| Gene Symbol: | ZNF280B ( 5'OY11.1,D87009.C22.3,SUHW2,ZNF279,ZNF632 ) |
|---|---|
| Gene Full Name: | zinc finger protein 280B |
| Band: | 22q11.22 |
| Quick Links | Entrez ID:140883; OMIM: NA; Uniprot ID:Z280B_HUMAN; ENSEMBL ID: ENSG00000198477; HGNC ID: 23022 |
| Relate to Another Database: | SFARIGene; denovo-db |
Variant Statistic TopClick the link of the category-specific score to view different category of evidences. The categories without any evidences are hidden by default. Chromosome coordinates: hg19
| Genetic Category | CNVs/SVs | de novo Mutations | Mosaics SNVs | NGS Other Mutations | Low-Scale Gene Mutations | Linkage Regions | Total |
|---|---|---|---|---|---|---|---|
| Number | 12 | 2 | 1 | 0 | 0 | 0 | 15 |
CNVs/SVs Top| CNV ID | Chr | Band | Start | End | Size | Gain/Loss | UCSC Browser | Reference |
|---|---|---|---|---|---|---|---|---|
| AutCNV0000269 | 22 | 22q11 | loss | Roubertie, 2001 | ||||
| AutCNV0000270 | 22 | 22q11 | loss | Niklasson, 2002 | ||||
| AutCNV0000392 | 22 | 22q11.2 | 17920000 | 25970000 | 8050000 | gain | external link | Ramelli, 2008 |
| AutCNV0000189 | 22 | 22q11.2 | 18890946 | 23222208 | 4331262 | gain | external link | Marshall, 2008 |
| AutCNV0000158 | 22 | 22q11.21 | 18890946 | 23222208 | 4331262 | gain | external link | Marshall, 2008 |
| AutCNV0000438 | 22 | 22q11.22 | 22735232 | 23260921 | 525689 | gain | external link | Gregory, 2009 |
| AutCNV0000437 | 22 | 22q11.22 | 22735232 | 23216472 | 481240 | gain | external link | Gregory, 2009 |
| AutCNV0000436 | 22 | 22q11.22 | 22699595 | 23260921 | 561326 | loss | external link | Gregory, 2009 |
| AutCNV0000435 | 22 | 22q11.22 | 22598241 | 23230820 | 632579 | loss | external link | Gregory, 2009 |
| AutCNV0000723 | 22 | 22q11.21-q11.22 | 21470000 | 23070000 | 1600000 | loss | external link | Bremer, 2011 |
| AutCNV0004392 | 22 | 22q11.21-q11.22 | 18885500 | 23216762 | 4331262 | gain | external link | Sanders, 2011 |
| AutCNV0004962 | 22 | 22q11.22 | loss | Hadley D, 2014 |
NGS de novo Mutations TopiFish (integrated Functional inference of SNVs in human) is based on gene/gene family customized models to classify missense mutations.
| Chr | Pos | Ref | Alt | Coding | AA | Validated Method | iFish Prediction | iFish Probability | Reference |
|---|---|---|---|---|---|---|---|---|---|
| 22 | 22842831 | T | C | Sanger sequencing | neutral | 0.157 | De Rubeis S, 2014 | ||
| 22 | 22842831 | T | C | c.893CAG>CGG | p.298Q>R | neutral | 0.157 | Fromer M, 2014 |
NGS Mosaic Mutations Top| Chr | Position | Ref | Alt | Genotype | Validated Method | Reference |
|---|---|---|---|---|---|---|
| 22 | 22843578 | A | C | Low-confidence mosaics | Resequencing | Lim ET, 2017 |
NGS Other Mutations Top| Chr | Pos | Ref | Alt | Coding | AA | Validated | iFish Prediction | iFish Probability | Reference |
|---|---|---|---|---|---|---|---|---|---|
| No related data! | |||||||||
Low-Scale Gene Mutations Top| Chr | Pos | Ref | Alt | Coding | AA | Validated | iFish Prediction | iFish Probability | Reference |
|---|---|---|---|---|---|---|---|---|---|
| No related data! | |||||||||
Linkage Regions Top| Linkage Name | Band | Chr | Marker | LOD | NPL | P Value | Reference |
|---|---|---|---|---|---|---|---|
| No related data! | |||||||