|   
  
    | Variant #0000692748 (NC_000019.9:g.33792565C>A, NM_004364.3:c.756G>T (CEBPA))
        
          | Chromosome | 19 |  
          | Allele | Unknown |  
          | Affects function (as reported) | Does not affect function |  
          | Affects function (by curator) | Not classified |  
          | Classification method | - |  
          | Clinical classification | benign |  
          | DNA change (genomic) (Relative to hg19 / GRCh37) | g.33792565C>A |  
          | DNA change (hg38) | - |  
          | Published as | CEBPA(NM_001285829.1):c.399G>T (p.(Ala133=)), CEBPA(NM_004364.3):c.756G>T (p.A252=), CEBPA(NM_004364.5):c.756G>T (p.A252=) |  
          | ISCN | - |  
          | DB-ID | CEBPA_000016 See all 3 reported entries |  
          | Variant remarks | VKGL data sharing initiative Nederland |  
          | Reference | - |  
          | ClinVar ID | - |  
          | dbSNP ID | - |  
          | Origin | CLASSIFICATION record |  
          | Segregation | - |  
          | Frequency | - |  
          | Re-site | - |  
          | VIP | - |  
          | Methylation | - |  
          | Average frequency (gnomAD v.2.1.1) | 0.00178 View details |  
          | Owner | VKGL-NL_Leiden |  
          | Database submission license | Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International   |  
          | Created by | VKGL-NL_Leiden |  
          | Date created | 2020-09-15 15:50:26 +02:00 (CEST) |  
          | Date last edited | 2025-02-07 18:57:27 +01:00 (CET) |   
 
 
 
       
 
 Variant on transcripts
 |  
 
    Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
    Use our APIs  to retrieve data.
 |