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    | Variant #0001008974 (NC_000001.10:g.94528311T>C, NC_000001.10(NM_000350.2):c.1761-2A>G (ABCA4))
        
          | Chromosome | 1 |  
          | Allele | Unknown |  
          | Affects function (as reported) | Affects function |  
          | Affects function (by curator) | Not classified |  
          | Classification method | ACMG |  
          | Clinical classification | pathogenic |  
          | DNA change (genomic) (Relative to hg19 / GRCh37) | g.94528311T>C |  
          | DNA change (hg38) | g.94062755T>C |  
          | Published as | - |  
          | ISCN | - |  
          | DB-ID | ABCA4_001138 See all 24 reported entries |  
          | Variant remarks | ACMG PVS1_S, PS4, PM3_S; severity category severe |  
          | Reference | Journal: Cornelis 2023 |  
          | ClinVar ID | - |  
          | dbSNP ID | - |  
          | Origin | SUMMARY record |  
          | Segregation | - |  
          | Frequency | - |  
          | Re-site | - |  
          | VIP | - |  
          | Methylation | - |  
          | Average frequency (gnomAD v.2.1.1) | Retrieve |  
          | Owner | Stéphanie Cornelis |  
          | Database submission license | Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International   |  
          | Created by | Johan den Dunnen |  
          | Date created | 2024-09-25 16:00:58 +02:00 (CEST) |  
          | Date last edited | N/A |   
 
 
 
       
 
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