| Variant #0000576026 (NC_000023.10:g.44732845_44732847dup, NM_021140.2:c.48_50dup (KDM6A))
        
          | Chromosome | X |  
          | 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.44732845_44732847dup |  
          | DNA change (hg38) | g.44873599_44873601dup |  
          | Published as | KDM6A(NM_001291415.1):c.48_50dupCGC (p.A17dup), KDM6A(NM_001291415.2):c.48_50dup (p.(Ala17dup)), KDM6A(NM_021140.4):c.48_50dupCGC (p.A17dup) |  
          | ISCN | - |  
          | DB-ID | KDM6A_000059 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) | Retrieve |  
          | Owner | VKGL-NL_Rotterdam |  
          | Database submission license | Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International   |  
          | Created by | VKGL-NL_Rotterdam |  
          | Date created | 2019-07-18 18:22:55 +02:00 (CEST) |  
          | Date last edited | 2024-04-19 20:27:30 +02:00 (CEST) |   
 
 
 
       
 
 Variant on transcripts
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