| Variant #0000150702 (NC_000007.13:g.75611597A>G, NM_000941.2:c.787A>G (POR))
        
          | Chromosome | 7 |  
          | Allele | Unknown |  
          | Affects function (as reported) | Probably affects function |  
          | Affects function (by curator) | Not classified |  
          | Classification method | - |  
          | Clinical classification | NA |  
          | DNA change (genomic) (Relative to hg19 / GRCh37) | g.75611597A>G |  
          | DNA change (hg38) | g.75982279A>G |  
          | Published as | M263V |  
          | ISCN | - |  
          | DB-ID | POR_000042 See all 4 reported entries |  
          | Variant remarks | cDNA expression cloning in bacteria showed cytochrome C reduction 0.76, NADPH oxidation 0.57 |  
          | Reference | PubMed: Huang 2005 |  
          | ClinVar ID | - |  
          | dbSNP ID | - |  
          | Origin | In vitro (cloned) |  
          | Segregation | - |  
          | Frequency | - |  
          | Re-site | - |  
          | VIP | - |  
          | Methylation | - |  
          | Average frequency (gnomAD v.2.1.1) | 2.0E-5 View details |  
          | Owner | Johan den Dunnen |  
          | Database submission license | Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International   |  
          | Created by | Johan den Dunnen |  
          | Date created | 2016-12-17 13:43:34 +01:00 (CET) |  
          | Date last edited | 2024-02-14 11:33:15 +01:00 (CET) |   
 
 
 
       
 
 Variant on transcripts
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