Variant Details for SLC22A18AS


Gene Symbol: | SLC22A18AS ( BWR1B,BWSCR1B,ORCTL2S,SLC22A1LS,p27-BWR1B ) |
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Gene Full Name: | solute carrier family 22 (organic cation transporter), member 18 antisense |
Band: | 11p15.4 |
Quick Links | Entrez ID:5003; OMIM: 603240; Uniprot ID:BWR1B_HUMAN; ENSEMBL ID: ENSG00000254827; HGNC ID: 10965 |
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 |
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Number | 2 | 0 | 0 | 0 | 0 | 0 | 2 |


CNV ID | Chr | Band | Start | End | Size | Gain/Loss | UCSC Browser | Reference |
---|---|---|---|---|---|---|---|---|
AutCNV0002272 | 11 | 11p15.4 | 2904010 | 2973880 | 69870 | loss | external link | Pinto, 2010 |
AutCNV0004915 | 21 | Tammimies K, 2015 |


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 |
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No related data! |


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


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


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


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