| Variant #0000621999 (NC_000008.10:g.140743340G>T, NM_001160372.1:c.3411C>A (TRAPPC9))
        
          | Chromosome | 8 |  
          | 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.140743340G>T |  
          | DNA change (hg38) | g.139731097G>T |  
          | Published as | TRAPPC9(NM_001321646.1):c.3384C>A (p.P1128=) |  
          | ISCN | - |  
          | DB-ID | TRAPPC9_000055 |  
          | 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) | 0.00029 View details |  
          | Owner | VKGL-NL_Rotterdam |  
          | Database submission license | Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International   |  
          | Created by | VKGL-NL_Rotterdam |  
          | Date created | 2019-12-06 12:43:26 +01:00 (CET) |  
          | Date last edited | 2022-11-01 13:01:21 +01:00 (CET) |   
 
 
 
       
 
 Variant on transcripts
 |