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    | Variant #0000914199 (NC_000014.8:g.55369176G>A, NM_000161.2:c.206C>T (GCH1))
        
          | Chromosome | 14 |  
          | Allele | Unknown |  
          | Affects function (as reported) | Effect unknown |  
          | Affects function (by curator) | Not classified |  
          | Classification method | - |  
          | Clinical classification | VUS |  
          | DNA change (genomic) (Relative to hg19 / GRCh37) | g.55369176G>A |  
          | DNA change (hg38) | - |  
          | Published as | GCH1(NM_000161.2):c.206C>T (p.P69L, p.(Pro69Leu)), GCH1(NM_000161.3):c.206C>T (p.P69L), GCH1(NM_001024024.1):c.206C>T (p.P69L) |  
          | ISCN | - |  
          | DB-ID | GCH1_000022 See all 5 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) | 0.00044 View details |  
          | Owner | VKGL-NL_Nijmegen |  
          | Database submission license | Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International   |  
          | Created by | VKGL-NL_Nijmegen |  
          | Date created | 2023-01-11 15:44:22 +01:00 (CET) |  
          | Date last edited | 2024-08-28 13:16:32 +02:00 (CEST) |   
 
 
 
       
 
 Variant on transcripts
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