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    | Variant #0000912346 (NC_000005.9:g.42695200C>T, NC_000005.9(NM_000163.4):c.439+9C>T (GHR))
        
          | Chromosome | 5 |  
          | 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.42695200C>T |  
          | DNA change (hg38) | - |  
          | Published as | GHR(NM_000163.4):c.439+9C>T (p.(=)) |  
          | ISCN | - |  
          | DB-ID | GHR_000127 |  
          | 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) | 0.00033 View details |  
          | Owner | VKGL-NL_Leiden |  
          | Database submission license | Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International   |  
          | Created by | VKGL-NL_Leiden |  
          | Date created | 2023-01-11 15:44:22 +01:00 (CET) |  
          | Date last edited | N/A |   
 
 
 
       
 
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