| Variant #0000277357 (NC_000012.11:g.65146532C>T, NM_002076.3:c.198G>A (GNS))
        
          | Chromosome | 12 |  
          | 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.65146532C>T |  
          | DNA change (hg38) | g.64752752C>T |  
          | Published as | GNS(NM_002076.3):c.198G>A (p.P66=), GNS(NM_002076.4):c.198G>A (p.P66=) |  
          | ISCN | - |  
          | DB-ID | GNS_000015 See all 4 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) | 0.6399 View details |  
          | Owner | VKGL-NL_AMC |  
          | Database submission license | Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International   |  
          | Created by | VKGL-NL_AMC |  
          | Date created | 2018-01-15 20:58:59 +01:00 (CET) |  
          | Date last edited | 2021-09-17 14:40:49 +02:00 (CEST) |   
 
 
 
       
 
 Variant on transcripts
 |