| Variant #0000999205 (NC_000011.9:g.62459867C>T, NM_001122955.3:c.844G>A (BSCL2))
        
          | Chromosome | 11 |  
          | Allele | Unknown |  
          | Affects function (as reported) | Probably does not affect function |  
          | Affects function (by curator) | Not classified |  
          | Classification method | - |  
          | Clinical classification | likely benign |  
          | DNA change (genomic) (Relative to hg19 / GRCh37) | g.62459867C>T |  
          | DNA change (hg38) | - |  
          | Published as | BSCL2(NM_001122955.3):c.844G>A (p.A282T), BSCL2(NM_001122955.4):c.844G>A (p.(Ala282Thr)), BSCL2(NM_001386027.1):c.844G>A (p.A282T) |  
          | ISCN | - |  
          | DB-ID | GNG3_000005 See all 4 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) | 3.0E-5 View details |  
          | Owner | VKGL-NL_AMC |  
          | Database submission license | Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International   |  
          | Created by | VKGL-NL_AMC |  
          | Date created | 2024-08-28 13:16:32 +02:00 (CEST) |  
          | Date last edited | N/A |   
 
 
 
       
 
 Variant on transcripts
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