| Variant #0000517343 (NC_000003.11:g.10183714C>G, NM_000551.3:c.183C>G (VHL))
        
          | Chromosome | 3 |  
          | 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.10183714C>G |  
          | DNA change (hg38) | g.10142030C>G |  
          | Published as | VHL(NM_000551.3):c.183C>G (p.P61=), VHL(NM_000551.4):c.183C>G (p.P61=) |  
          | ISCN | - |  
          | DB-ID | VHL_000573 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) | 0.001 View details |  
          | 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 | 2023-04-16 21:50:28 +02:00 (CEST) |   
 
 
 
       
 
 Variant on transcripts
 |