| Variant #0000191041 (NC_000017.10:g.41276059G>A, NM_007294.3:c.55C>T (BRCA1))
        
          | Chromosome | 17 |  
          | Allele | Parent #1 |  
          | Affects function (as reported) | Affects function |  
          | Affects function (by curator) | Affects function |  
          | Classification method | - |  
          | Clinical classification | pathogenic (dominant) |  
          | DNA change (genomic) (Relative to hg19 / GRCh37) | g.41276059G>A |  
          | DNA change (hg38) | g.43124042G>A |  
          | Published as | - |  
          | ISCN | - |  
          | DB-ID | BRCA1_004571 See all 2 reported entries |  
          | Variant remarks | Variant allele predicted to encode truncated non-functional protein |  
          | Reference | ENIGMA classification criteria |  
          | ClinVar ID | - |  
          | dbSNP ID | - |  
          | Origin | SUMMARY record |  
          | Segregation | - |  
          | Frequency | - |  
          | Re-site | - |  
          | VIP | - |  
          | Methylation | - |  
          | Average frequency (gnomAD v.2.1.1) | Retrieve |  
          | Owner | ENIGMA consortium |  
          | Database submission license | Creative Commons Attribution 4.0 International   |  
          | Created by | ENIGMA consortium |  
          | Date created | 2016-10-18 12:00:00 +02:00 (CEST) |  
          | Date last edited | 2024-10-24 10:44:58 +02:00 (CEST) |   
 
 
 
       
 
 Variant on transcripts
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