| Variant #0000549164 (NC_000012.11:g.76741496dup, NM_024685.3:c.271dup (BBS10))
        
          | Chromosome | 12 |  
          | 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.76741496dup |  
          | DNA change (hg38) | g.76347716dup |  
          | Published as | BBS10(NM_024685.4):c.271dup (p.(Cys91LeufsTer5)), BBS10(NM_024685.4):c.271dupT (p.C91Lfs*5) |  
          | ISCN | - |  
          | DB-ID | BBS10_000092 See all 5 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_AMC |  
          | Database submission license | Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International   |  
          | Created by | VKGL-NL_AMC |  
          | Date created | 2019-07-18 18:22:55 +02:00 (CEST) |  
          | Date last edited | 2024-04-19 20:27:30 +02:00 (CEST) |   
 
 
 
       
 
 Variant on transcripts
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