|   
  
    | Variant #0000920439 (NC_000002.11:g.99006106T>G, NC_000002.11(NM_001298.2):c.450-15T>G (CNGA3))
        
          | Chromosome | 2 |  
          | Allele | Unknown |  
          | Affects function (as reported) | Affects function |  
          | Affects function (by curator) | Not classified |  
          | Classification method | - |  
          | Clinical classification | NA |  
          | DNA change (genomic) (Relative to hg19 / GRCh37) | g.99006106T>G |  
          | DNA change (hg38) | g.98389643T>G |  
          | Published as | - |  
          | ISCN | - |  
          | DB-ID | CNGA3_000259 See all 3 reported entries |  
          | Variant remarks | analysis variant in in vitro mini-gene splicing assay |  
          | Reference | PubMed: Reuter 2021 |  
          | ClinVar ID | - |  
          | dbSNP ID | - |  
          | Origin | In vitro (cloned) |  
          | Segregation | - |  
          | Frequency | - |  
          | Re-site | - |  
          | VIP | - |  
          | Methylation | - |  
          | Average frequency (gnomAD v.2.1.1) | Retrieve |  
          | Owner | Johan den Dunnen |  
          | Database submission license | Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International   |  
          | Created by | Johan den Dunnen |  
          | Date created | 2023-03-02 15:48:44 +01:00 (CET) |  
          | Date last edited | N/A |   
 
 
 
       
 
 Variant on transcripts
 |  
 
    Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
    Use our APIs  to retrieve data.
 |