| Variant #0000677728 (NC_000006.11:g.31915584A>C, NM_006929.4:c.-11386A>C (SKIV2L))
        
          | Chromosome | 6 |  
          | 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.31915584A>C |  
          | DNA change (hg38) | - |  
          | Published as | CFB(NM_001710.5):c.724A>C (p.I242L, p.(Ile242Leu)), CFB(NM_001710.6):c.724A>C (p.I242L) |  
          | ISCN | - |  
          | DB-ID | C2_000018 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) | 0.00097 View details |  
          | Owner | VKGL-NL_Utrecht |  
          | Database submission license | Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International   |  
          | Created by | VKGL-NL_Utrecht |  
          | Date created | 2020-08-06 14:59:34 +02:00 (CEST) |  
          | Date last edited | 2024-08-28 13:16:32 +02:00 (CEST) |   
 
 
 
       
 
 Variant on transcripts
 |