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    | Variant #0000314811 (NC_000011.9:g.6637759del, NC_000011.9(NM_000391.3):c.887-6del (TPP1))
        
          | Chromosome | 11 |  
          | 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.6637759del |  
          | DNA change (hg38) | g.6616528del |  
          | Published as | TPP1(NM_000391.3):c.887-6delA, TPP1(NM_000391.3):c.887-6delA (p.(=)), TPP1(NM_000391.4):c.887-6delA |  
          | ISCN | - |  
          | DB-ID | TPP1_000136 See all 4 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 | 2018-01-15 20:58:59 +01:00 (CET) |  
          | Date last edited | 2022-05-09 15:24:52 +02:00 (CEST) |   
 
 
 
       
 
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