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    | Variant #0000895167 (NC_000019.9:g.6714079C>T, NM_000064.2:c.697G>A (C3))
        
          | Chromosome | 19 |  
          | Allele | Unknown |  
          | Affects function (as reported) | Effect unknown |  
          | Affects function (by curator) | Not classified |  
          | Classification method | - |  
          | Clinical classification | VUS |  
          | DNA change (genomic) (Relative to hg19 / GRCh37) | g.6714079C>T |  
          | DNA change (hg38) | - |  
          | Published as | C3(NM_000064.2):c.697G>A (p.E233K) |  
          | ISCN | - |  
          | DB-ID | C3_000023 See all 2 reported entries |  
          | Variant remarks | VKGL data sharing initiative Nederland |  
          | Reference | - |  
          | ClinVar ID | - |  
          | dbSNP ID | - |  
          | Origin | CLASSIFICATION record |  
          | Segregation | - |  
          | Frequency | - |  
          | Re-site | - |  
          | VIP | - |  
          | Methylation | - |  
          | Average frequency (gnomAD v.2.1.1) | 2.0E-5 View details |  
          | Owner | VKGL-NL_Utrecht |  
          | Database submission license | Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International   |  
          | Created by | VKGL-NL_Utrecht |  
          | Date created | 2022-11-01 13:41:49 +01:00 (CET) |  
          | Date last edited | N/A |   
 
 
 
       
 
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