| Variant #0000332108 (NC_000008.10:g.38871509G>A, NM_003816.2:c.280G>A (ADAM9))
        
          | Chromosome | 8 |  
          | 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.38871509G>A |  
          | DNA change (hg38) | g.39013990G>A |  
          | Published as | ADAM9(NM_003816.2):c.280G>A (p.V94I, p.(Val94Ile)), ADAM9(NM_003816.3):c.280G>A (p.V94I) |  
          | ISCN | - |  
          | DB-ID | ADAM9_000002 See all 5 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) | 0.0021 View details |  
          | 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 | 2025-02-07 18:57:27 +01:00 (CET) |   
 
 
 
       
 
 Variant on transcripts
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