| Variant #0000616068 (NC_000016.9:g.67208692_67208697dup, NM_001040715.1:c.*2027_*2032dup (KIAA0895L))
        
          | Chromosome | 16 |  
          | 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.67208692_67208697dup |  
          | DNA change (hg38) | g.67174789_67174794dup |  
          | Published as | NOL3(NM_001276312.1):c.464_469dupCAGAGC (p.P155_E156dup) |  
          | ISCN | - |  
          | DB-ID | FBXL8_000012 |  
          | 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_Rotterdam |  
          | Database submission license | Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International   |  
          | Created by | VKGL-NL_Rotterdam |  
          | Date created | 2019-12-04 15:24:38 +01:00 (CET) |  
          | Date last edited | 2020-08-06 14:59:34 +02:00 (CEST) |   
 
 
 
       
 
 Variant on transcripts
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