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    | Variant #0000892523 (NC_000016.9:g.14028081C>T, NM_005236.2:c.1135C>T (ERCC4))
        
          | Chromosome | 16 |  
          | Allele | Unknown |  
          | Affects function (as reported) | Does not affect function |  
          | Affects function (by curator) | Not classified |  
          | Classification method | - |  
          | Clinical classification | benign |  
          | DNA change (genomic) (Relative to hg19 / GRCh37) | g.14028081C>T |  
          | DNA change (hg38) | - |  
          | Published as | ERCC4(NM_005236.2):c.1135C>T (p.P379S, p.(Pro379Ser)), ERCC4(NM_005236.3):c.1135C>T (p.P379S) |  
          | ISCN | - |  
          | DB-ID | ERCC4_000037 See all 8 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) | 0.00396 View details |  
          | Owner | VKGL-NL_Utrecht |  
          | Database submission license | Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International   |  
          | Created by | VKGL-NL_Utrecht |  
          | Date created | 2022-11-01 13:41:49 +01:00 (CET) |  
          | Date last edited | 2023-01-11 15:44:22 +01:00 (CET) |   
 
 
 
       
 
 Variant on transcripts
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