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    | Variant #0000126925 (NC_000001.10:g.94586599_94586601delinsGAC, NM_000350.2:c.1_3delinsGTC (ABCA4))
        
          | Chromosome | 1 |  
          | Allele | Parent #1 |  
          | Affects function (as reported) | Effect unknown |  
          | Affects function (by curator) | Not classified |  
          | Classification method | ACMG |  
          | Clinical classification | VUS |  
          | DNA change (genomic) (Relative to hg19 / GRCh37) | g.94586599_94586601delinsGAC |  
          | DNA change (hg38) | g.94121043_94121045delinsGAC |  
          | Published as | - |  
          | ISCN | - |  
          | DB-ID | ABCA4_000262 See all 2 reported entries |  
          | Variant remarks | - |  
          | Reference | PubMed: Cornelis 2017, Journal: Cornelis 2017, 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 4.0 International   |  
          | Created by | Stéphanie Cornelis |  
          | Date created | 2016-07-29 12:46:24 +02:00 (CEST) |  
          | Date last edited | 2024-09-25 14:18:42 +02:00 (CEST) |   
 
 
 
       
 
 Variant on transcripts
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