Variant #0000867194 (NC_000023.10:g.153297746C>T, NM_004992.3:c.289G>A (MECP2))
      
      
        
          | Chromosome | 
          X |  
        
          | Allele | 
          Unknown |  
        
          | Affects function (as reported) | 
          Affects function |  
        
          | Affects function (by curator) | 
          Not classified |  
        
          | Classification method | 
          - |  
        
          | Clinical classification | 
          pathogenic |  
        
          | DNA change (genomic) (Relative to hg19 / GRCh37) | 
          g.153297746C>T |  
        
          | DNA change (hg38) | 
          - |  
        
          | Published as | 
          MECP2(NM_001369391.2):c.10G>A (p.D4N) |  
        
          | ISCN | 
          - |  
        
          | DB-ID | 
          MECP2_002943 |  
        
          | 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) | 
          Retrieve |  
        
          | Owner | 
          VKGL-NL_VUmc |  
        
          | Database submission license | 
          Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International   |  
        
          | Created by | 
          VKGL-NL_VUmc |  
        
          | Date created | 
          2022-05-09 16:01:56 +02:00 (CEST) |  
        
          | Date last edited | 
          N/A |   
        
      
      
      
  
      
       
      
  
      Variant on transcripts
      
      
       
      
      
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