Variant Details for RGS22


Gene Symbol: | RGS22 ( DKFZp434I092,FLJ40080,FLJ75004,MGC102908,PRTD-NY2 ) |
---|---|
Gene Full Name: | regulator of G-protein signaling 22 |
Band: | 8q22.2 |
Quick Links | Entrez ID:26166; OMIM: NA; Uniprot ID:RGS22_HUMAN; ENSEMBL ID: ENSG00000132554; HGNC ID: 24499 |
Relate to Another Database: | SFARIGene; denovo-db |


Click 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 | 2 | 1 | 0 | 0 | 0 | 0 | 3 |


CNV ID | Chr | Band | Start | End | Size | Gain/Loss | UCSC Browser | Reference |
---|---|---|---|---|---|---|---|---|
AutCNV0000533 | 8 | 8q22.2 | 101054263 | 101693386 | 639123 | gain | external link | Gregory, 2009 |
AutCNV0001912 | 8 | 8q22.2 | 101093252 | 101183535 | 90283 | gain | external link | Pinto, 2010 |


iFish (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 |
---|---|---|---|---|---|---|---|---|---|
8 | 100990260 | C | M | Sanger sequencing | O'Roak BJ, 2012 |


Chr | Position | Ref | Alt | Genotype | Validated Method | Reference |
---|---|---|---|---|---|---|
No related data! |


Chr | Pos | Ref | Alt | Coding | AA | Validated | iFish Prediction | iFish Probability | Reference |
---|---|---|---|---|---|---|---|---|---|
No related data! |


Chr | Pos | Ref | Alt | Coding | AA | Validated | iFish Prediction | iFish Probability | Reference |
---|---|---|---|---|---|---|---|---|---|
No related data! |


Linkage Name | Band | Chr | Marker | LOD | NPL | P Value | Reference |
---|---|---|---|---|---|---|---|
No related data! |