| Variant #0000569812 (NC_000020.10:g.44520261_44520263dup, NM_001278535.1:c.-610_-608dup (NEURL2))
        
          | Chromosome | 20 |  
          | 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.44520261_44520263dup |  
          | DNA change (hg38) | g.45891622_45891624dup |  
          | Published as | CTSA(NM_000308.2):c.108_110dup (p.(Leu37dup)), CTSA(NM_001127695.2):c.54_56dupGCT (p.L19dup), CTSA(NM_001127695.3):c.54_56dupGCT (p.L19dup) |  
          | ISCN | - |  
          | DB-ID | CTSA_000020 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) | Retrieve |  
          | Owner | VKGL-NL_Rotterdam |  
          | Database submission license | Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International   |  
          | Created by | VKGL-NL_Rotterdam |  
          | Date created | 2019-07-18 18:22:55 +02:00 (CEST) |  
          | Date last edited | 2023-04-16 21:50:28 +02:00 (CEST) |   
 
 
 
       
 
 Variant on transcripts
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