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    | Variant #0000328582 (NC_000020.10:g.61444855_61444914del, NM_001853.3:c.-3562_-3503del (COL9A3))
        
          | Chromosome | 20 |  
          | 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.61444855_61444914del |  
          | DNA change (hg38) | g.62813503_62813562del |  
          | Published as | OGFR(NM_007346.2):c.1874_1933del (p.(Ala627_Pro646del)) |  
          | ISCN | - |  
          | DB-ID | OGFR_000015 |  
          | 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_Leiden |  
          | Database submission license | Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International   |  
          | Created by | VKGL-NL_Leiden |  
          | Date created | 2018-01-15 20:58:59 +01:00 (CET) |  
          | Date last edited | 2020-03-23 16:13:27 +01:00 (CET) |   
 
 
 
       
 
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