| Variant #0000517351 (NC_000003.11:g.10183790_10183791insA, NM_000551.3:c.259_260insA (VHL))
        
          | Chromosome | 3 |  
          | 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.10183790_10183791insA |  
          | DNA change (hg38) | g.10142106_10142107insA |  
          | Published as | VHL(NM_000551.3):c.259_260insA (p.V87Dfs*45) |  
          | ISCN | - |  
          | DB-ID | VHL_000579 |  
          | 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 | 2019-07-18 18:22:55 +02:00 (CEST) |  
          | Date last edited | 2020-06-12 11:59:05 +02:00 (CEST) |   
 
 
 
       
 
 Variant on transcripts
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