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    | Variant #0000314474 (NC_000022.10:g.31018958T>G, NM_000355.3:c.1110T>G (TCN2))
        
          | Chromosome | 22 |  
          | Allele | Unknown |  
          | Affects function (as reported) | Affects function |  
          | Affects function (by curator) | Not classified |  
          | Classification method | - |  
          | Clinical classification | pathogenic |  
          | DNA change (genomic) (Relative to hg19 / GRCh37) | g.31018958T>G |  
          | DNA change (hg38) | g.30622971T>G |  
          | Published as | TCN2(NM_001184726.1):c.1029T>G (p.Y343*) |  
          | ISCN | - |  
          | DB-ID | TCN2_000006 |  
          | 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_Utrecht |  
          | Database submission license | Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International   |  
          | Created by | VKGL-NL_Utrecht |  
          | Date created | 2018-01-15 20:58:59 +01:00 (CET) |  
          | Date last edited | 2020-07-17 12:03:04 +02:00 (CEST) |   
 
 
 
       
 
 Variant on transcripts
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