| Variant #0000553464 (NC_000014.8:g.94849388G>A, NM_001127701.1:c.187C>T (SERPINA1))
        
          | 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.94849388G>A |  
          | DNA change (hg38) | g.94383051G>A |  
          | Published as | SERPINA1(NM_000295.4):c.187C>T (p.(Arg63Cys)), SERPINA1(NM_001127701.1):c.187C>T (p.R63C), SERPINA1(NM_001127701.2):c.187C>T (p.R63C) |  
          | ISCN | - |  
          | DB-ID | SERPINA1_000005 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) | 0.00104 View details |  
          | Owner | VKGL-NL_Groningen |  
          | Database submission license | Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International   |  
          | Created by | VKGL-NL_Groningen |  
          | Date created | 2019-07-18 18:22:55 +02:00 (CEST) |  
          | Date last edited | 2022-05-09 15:51:19 +02:00 (CEST) |   
 
 
 
       
 
 Variant on transcripts
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