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    | Variant #0000018020 (NC_000001.10:g.171072929C>A, NM_001002294.2:c.136C>A (FMO3))
        
          | Individual ID | 00103143 |  
          | Chromosome | 1 |  
          | Allele | Unknown |  
          | Affects function (as reported) | Does not affect function |  
          | Affects function (by curator) | Does not affect function |  
          | Classification method | - |  
          | Clinical classification | benign |  
          | DNA change (genomic) (Relative to hg19 / GRCh37) | g.171072929C>A |  
          | DNA change (hg38) | g.171103788C>A |  
          | Published as | - |  
          | ISCN | - |  
          | DB-ID | FMO3_000046 |  
          | Variant remarks | Rare variant. 1/140 chromosomes in Koreans |  
          | Reference | PubMed: Park et al. 1999 |  
          | ClinVar ID | - |  
          | dbSNP ID | - |  
          | Origin | Germline |  
          | Segregation | no |  
          | Frequency | 1/140 chromosomes |  
          | Re-site | - |  
          | VIP | - |  
          | Methylation | - |  
          | Average frequency (gnomAD v.2.1.1) | Retrieve |  
          | Owner | Ornicha Prapapan |  
          | Database submission license | No license selected |  
          | Created by | Ornicha Prapapan |  
          | Date created | 2013-05-13 14:08:46 +02:00 (CEST) |  
          | Date last edited | 2017-04-05 10:54:58 +02:00 (CEST) |   
 
 
 
       
 
 Variant on transcripts
 
 
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