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    | Variant #0000723795 (NC_000012.11:g.106821117T>C, NM_018082.5:c.1244T>C (POLR3B))
        
          | Chromosome | 12 |  
          | Allele | Unknown |  
          | Affects function (as reported) | Probably affects function |  
          | Affects function (by curator) | Not classified |  
          | Classification method | - |  
          | Clinical classification | likely pathogenic |  
          | DNA change (genomic) (Relative to hg19 / GRCh37) | g.106821117T>C |  
          | DNA change (hg38) | - |  
          | Published as | POLR3B(NM_018082.5):c.1244T>C (p.M415T), POLR3B(NM_018082.6):c.1244T>C (p.(Met415Thr), p.M415T) |  
          | ISCN | - |  
          | DB-ID | POLR3B_000032 See all 8 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) | 0.00056 View details |  
          | Owner | VKGL-NL_VUmc |  
          | Database submission license | Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International   |  
          | Created by | VKGL-NL_VUmc |  
          | Date created | 2021-02-08 18:36:18 +01:00 (CET) |  
          | Date last edited | 2024-04-19 20:27:30 +02:00 (CEST) |   
 
 
 
       
 
 Variant on transcripts
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