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    | Variant #0000984896 (NC_012920.1:m.14279G>A, NC_012920.1(ATP6_v001):c.*5072G>A (MT-ATP6))
        
          | Chromosome | M |  
          | 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) | m.14279G>A |  
          | DNA change (hg38) | - |  
          | Published as | MT-ND6(ENST00000361681.2):c.395C>T (p.(Ser132Leu)) |  
          | ISCN | - |  
          | DB-ID | MT-CO1_000008 |  
          | 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_Leiden |  
          | Database submission license | Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International   |  
          | Created by | VKGL-NL_Leiden |  
          | Date created | 2024-04-19 20:27:30 +02:00 (CEST) |  
          | Date last edited | N/A |   
 
 
 
       
 
 Variant on transcripts
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