| Variant #0000888318 (NC_000008.10:g.27319168G>T, NM_000742.3:c.1568C>A (CHRNA2))
        
          | Chromosome | 8 |  
          | 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.27319168G>T |  
          | DNA change (hg38) | - |  
          | Published as | CHRNA2(NM_000742.3):c.1568C>A (p.P523Q, p.(Pro523Gln)) |  
          | ISCN | - |  
          | DB-ID | CHRNA2_000036 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) | 1.0E-5 View details |  
          | Owner | VKGL-NL_VUmc |  
          | Database submission license | Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International   |  
          | Created by | VKGL-NL_VUmc |  
          | Date created | 2022-11-01 13:01:21 +01:00 (CET) |  
          | Date last edited | 2024-08-28 13:16:32 +02:00 (CEST) |   
 
 
 
       
 
 Variant on transcripts
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