| Variant #0000619140 (NC_000023.10:g.151900113C>T, NM_001102576.1:c.-3227C>T (CSAG1))
        
          | Chromosome | X |  
          | 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.151900113C>T |  
          | DNA change (hg38) | g.152736847= |  
          | Published as | MAGEA12(NM_001166386.3):c.688G>A (p.A230T) |  
          | ISCN | - |  
          | DB-ID | MAGEA12_000017 |  
          | 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) | 6.0E-5 View details |  
          | 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 | 2025-07-08 13:22:38 +02:00 (CEST) |   
 
 
 
       
 
 Variant on transcripts
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