| Variant #0000019559 (NC_000001.10:g.171059701A>G, NM_001002294.2:c.-428A>G (FMO3))
        
          | Chromosome | 1 |  
          | Allele | Unknown |  
          | Affects function (as reported) | Effect unknown |  
          | Affects function (by curator) | Effect unknown |  
          | Classification method | - |  
          | Clinical classification | VUS |  
          | DNA change (genomic) (Relative to hg19 / GRCh37) | g.171059701A>G |  
          | DNA change (hg38) | g.171090560A>G |  
          | Published as | -2099A>G |  
          | ISCN | - |  
          | DB-ID | FMO3_000100 |  
          | Variant remarks | effect unknown |  
          | Reference | PubMed: Koukouritaki et al. 2005 |  
          | ClinVar ID | - |  
          | dbSNP ID | - |  
          | Origin | Germline |  
          | Segregation | ? |  
          | Frequency | 0/1204 control chromosomes |  
          | Re-site | - |  
          | VIP | - |  
          | Methylation | - |  
          | Average frequency (gnomAD v.2.1.1) | Retrieve |  
          | Owner | Ian Phillips |  
          | Database submission license | No license selected |  
          | Created by | Ian Phillips |  
          | Date created | 2013-08-14 16:17:21 +02:00 (CEST) |  
          | Date last edited | 2017-04-05 11:00:42 +02:00 (CEST) |   
 
 
 
       
 
 Variant on transcripts
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