| Variant #0000854996 (NC_000017.10:g.48669450G>A, NM_018896.4:c.2907G>A (CACNA1G))
        
          | Chromosome | 17 |  
          | 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.48669450G>A |  
          | DNA change (hg38) | - |  
          | Published as | CACNA1G(NM_018896.4):c.2907G>A (p.A969=), CACNA1G(NM_018896.5):c.2907G>A (p.A969=) |  
          | ISCN | - |  
          | DB-ID | CACNA1G_000081 See all 2 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) | 0.00065 View details |  
          | Owner | VKGL-NL_Utrecht |  
          | Database submission license | Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International   |  
          | Created by | VKGL-NL_Utrecht |  
          | Date created | 2022-05-09 15:47:41 +02:00 (CEST) |  
          | Date last edited | N/A |   
 
 
 
       
 
 Variant on transcripts
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