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    | Variant #0000859652 (NC_000005.9:g.112043492C>A, NM_000038.5:c.-30149C>A (APC))
        
          | Chromosome | 5 |  
          | 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.112043492C>A |  
          | DNA change (hg38) | - |  
          | Published as | APC(NM_001127511.2):c.78C>A (p.(Ser26Arg)), APC(NM_001354897.2):c.78C>A (p.S26R) |  
          | ISCN | - |  
          | DB-ID | APC_001971 See all 2 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) | 0.00191 View details |  
          | Owner | VKGL-NL_Leiden |  
          | Database submission license | Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International   |  
          | Created by | VKGL-NL_Leiden |  
          | Date created | 2022-05-09 15:51:19 +02:00 (CEST) |  
          | Date last edited | 2024-04-19 20:27:30 +02:00 (CEST) |   
 
 
 
       
 
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