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    | Variant #0001016991 (NC_000005.9:g.(?_112111320)_(112179829_?)del, NM_000038.5:c.(?_423-6)_(*6_?)del (APC))
        
          | Chromosome | 5 |  
          | Allele | Unknown |  
          | Affects function (as reported) | Probably affects function |  
          | Affects function (by curator) | Not classified |  
          | Classification method | ACMG |  
          | Clinical classification | likely pathogenic |  
          | DNA change (genomic) (Relative to hg19 / GRCh37) | g.(?_112111320)_(112179829_?)del |  
          | DNA change (hg38) | g.(?_112775623)_(112844132_?)del |  
          | Published as | del ex5-16 |  
          | ISCN | - |  
          | DB-ID | APC_002254 |  
          | Variant remarks | ACMG PVS1, PM2_sup |  
          | Reference | PubMed: Yin 2024, Journal: Yin 2024 |  
          | ClinVar ID | ClinVar-469690 |  
          | dbSNP ID | - |  
          | Origin | SUMMARY record |  
          | Segregation | - |  
          | Frequency | - |  
          | Re-site | - |  
          | VIP | - |  
          | Methylation | - |  
          | Average frequency (gnomAD v.2.1.1) | Retrieve |  
          | Owner | Stefan Aretz |  
          | Database submission license | Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International   |  
          | Created by | Johan den Dunnen |  
          | Date created | 2024-11-14 12:22:32 +01:00 (CET) |  
          | Date last edited | N/A |   
 
 
 
       
 
 Variant on transcripts
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