|   
  
    | Variant #0000927383 (NC_000023.10:g.48542822_48542823dup, NC_000023.10(NM_000377.2):c.273+10_273+11dup (WAS))
        
          | Chromosome | X |  
          | Allele | Unknown |  
          | Affects function (as reported) | Probably does not affect function |  
          | Affects function (by curator) | Not classified |  
          | Classification method | - |  
          | Clinical classification | likely benign |  
          | DNA change (genomic) (Relative to hg19 / GRCh37) | g.48542822_48542823dup |  
          | DNA change (hg38) | - |  
          | Published as | WAS(NM_000377.2):c.273+10_273+11dupCC, WAS(NM_000377.2):c.273+10_273+11dupCC (p.?), WAS(NM_000377.2):c.273+9_273+10dupCC |  
          | ISCN | - |  
          | DB-ID | WAS_000044 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_Utrecht |  
          | Database submission license | Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International   |  
          | Created by | VKGL-NL_Utrecht |  
          | Date created | 2023-04-16 21:50:28 +02:00 (CEST) |  
          | Date last edited | 2025-02-07 18:57:27 +01:00 (CET) |   
 
 
 
       
 
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