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    | Variant #0000255925 (NC_000011.9:g.45948366del, NM_001101802.1:c.*7154del (PHF21A))
        
          | Chromosome | 11 |  
          | Allele | Unknown |  
          | Affects function (as reported) | Effect unknown |  
          | Affects function (by curator) | Not classified |  
          | Classification method | - |  
          | Clinical classification | VUS |  
          | DNA change (genomic) (Relative to hg19 / GRCh37) | g.45948366del |  
          | DNA change (hg38) | g.45926815del |  
          | Published as | LARGE2(NM_152312.4):c.1269delA (p.E423Dfs*35) |  
          | ISCN | - |  
          | DB-ID | GYLTL1B_000004 |  
          | 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 | 2018-01-15 20:58:59 +01:00 (CET) |  
          | Date last edited | 2020-06-30 13:18:24 +02:00 (CEST) |   
 
 
 
       
 
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