| Variant #0000174909 (NC_000003.11:g.8775642G>A, NM_033337.2:c.80G>A (CAV3))
        
          | Chromosome | 3 |  
          | Allele | Unknown |  
          | Affects function (as reported) | Affects function |  
          | Affects function (by curator) | Not classified |  
          | Classification method | - |  
          | Clinical classification | NA |  
          | DNA change (genomic) (Relative to hg19 / GRCh37) | g.8775642G>A |  
          | DNA change (hg38) | g.8733956G>A |  
          | Published as | R26Q |  
          | ISCN | - |  
          | DB-ID | CAV3_000007 See all 34 reported entries |  
          | Variant remarks | expression cloning C2C12 cells, CAV3-GFP retention in Golgi influencing MG53/DYSF localisation, defective membrane repair |  
          | Reference | PubMed: Cai 20029 |  
          | ClinVar ID | - |  
          | dbSNP ID | - |  
          | Origin | In vitro (cloned) |  
          | Segregation | - |  
          | Frequency | - |  
          | Re-site | - |  
          | VIP | - |  
          | Methylation | - |  
          | Average frequency (gnomAD v.2.1.1) | Retrieve |  
          | Owner | Johan den Dunnen |  
          | Database submission license | Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International   |  
          | Created by | Johan den Dunnen |  
          | Date created | 2012-04-15 15:58:24 +02:00 (CEST) |  
          | Date last edited | 2020-07-14 21:50:58 +02:00 (CEST) |   
 
 
 
       
 
 Variant on transcripts
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