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    | Variant #0000949605 (NC_000011.9:g.119210455G>T, NM_001278431.1:c.318C>A (C1QTNF5))
        
          | Chromosome | 11 |  
          | 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.119210455G>T |  
          | DNA change (hg38) | - |  
          | Published as | C1QTNF5(NM_015645.5):c.318C>A (p.F106L) |  
          | ISCN | - |  
          | DB-ID | RNF26_000008 |  
          | 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) | Retrieve |  
          | Owner | VKGL-NL_AMC |  
          | Database submission license | Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International   |  
          | Created by | VKGL-NL_AMC |  
          | Date created | 2023-11-27 17:35:39 +01:00 (CET) |  
          | Date last edited | 2024-02-26 20:06:56 +01:00 (CET) |   
 
 
 
       
 
 Variant on transcripts
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