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    | Variant #0000959719 (NC_000014.8:g.36986926C>T, NM_003317.3:c.673G>A (NKX2-1))
        
          | Chromosome | 14 |  
          | Allele | Unknown |  
          | Affects function (as reported) | Probably affects function |  
          | Affects function (by curator) | Not classified |  
          | Classification method | - |  
          | Clinical classification | likely pathogenic |  
          | DNA change (genomic) (Relative to hg19 / GRCh37) | g.36986926C>T |  
          | DNA change (hg38) | - |  
          | Published as | - |  
          | ISCN | - |  
          | DB-ID | NKX2-1_000042 |  
          | Variant remarks | - |  
          | Reference | - |  
          | ClinVar ID | - |  
          | dbSNP ID | rs2139407155 |  
          | Origin | CLASSIFICATION record |  
          | Segregation | - |  
          | Frequency | - |  
          | Re-site | - |  
          | VIP | - |  
          | Methylation | - |  
          | Average frequency (gnomAD v.2.1.1) | Retrieve |  
          | Owner | MobiDetails |  
          | Database submission license | Creative Commons Attribution 4.0 International   |  
          | Created by | MobiDetails |  
          | Date created | 2024-02-01 18:26:01 +01:00 (CET) |  
          | Date last edited | N/A |   
 
 
 
       
 
 Variant on transcripts
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