| Variant #0000804131 (NC_000009.11:g.368021C>A, NM_203447.3:c.1683C>A (DOCK8))
        
          | Chromosome | 9 |  
          | 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.368021C>A |  
          | DNA change (hg38) | - |  
          | Published as | DOCK8(NM_001190458.1):c.1479C>A (p.(Asn493Lys)), DOCK8(NM_203447.3):c.1683C>A (p.N561K), DOCK8(NM_203447.4):c.1683C>A (p.N561K) |  
          | ISCN | - |  
          | DB-ID | C9orf66_000016 See all 3 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) | 0.00011 View details |  
          | Owner | VKGL-NL_Groningen |  
          | Database submission license | Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International   |  
          | Created by | VKGL-NL_Groningen |  
          | Date created | 2021-09-17 14:40:49 +02:00 (CEST) |  
          | Date last edited | 2023-01-11 15:44:22 +01:00 (CET) |   
 
 
 
       
 
 Variant on transcripts
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