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    | Variant #0000931668 (NC_000015.9:g.49059645A>C, NM_001194998.1:c.2034T>G (CEP152))
        
          | Chromosome | 15 |  
          | Allele | Unknown |  
          | Affects function (as reported) | Affects function |  
          | Affects function (by curator) | Not classified |  
          | Classification method | - |  
          | Clinical classification | pathogenic |  
          | DNA change (genomic) (Relative to hg19 / GRCh37) | g.49059645A>C |  
          | DNA change (hg38) | - |  
          | Published as | - |  
          | ISCN | - |  
          | DB-ID | CEP152_000004 See all 3 reported entries |  
          | Variant remarks | - |  
          | Reference | - |  
          | ClinVar ID | - |  
          | dbSNP ID | rs182018947 |  
          | Origin | Unknown |  
          | Segregation | - |  
          | Frequency | - |  
          | Re-site | - |  
          | VIP | - |  
          | Methylation | - |  
          | Average frequency (gnomAD v.2.1.1) | 0.00028 View details |  
          | Owner | MobiDetails |  
          | Database submission license | Creative Commons Attribution 4.0 International   |  
          | Created by | MobiDetails |  
          | Date created | 2023-08-01 23:30:01 +02:00 (CEST) |  
          | Date last edited | N/A |   
 
 
 
       
 
 Variant on transcripts
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