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    | Variant #0000982336 (NC_000017.10:g.16843729G>T, NM_012452.2:c.542C>A (TNFRSF13B))
        
          | Chromosome | 17 |  
          | Allele | Unknown |  
          | Affects function (as reported) | Effect unknown |  
          | Affects function (by curator) | Not classified |  
          | Classification method | - |  
          | Clinical classification | VUS |  
          | DNA change (genomic) (Relative to hg19 / GRCh37) | g.16843729G>T |  
          | DNA change (hg38) | - |  
          | Published as | TNFRSF13B(NM_012452.2):c.542C>A (p.A181E), TNFRSF13B(NM_012452.3):c.542C>A (p.(Ala181Glu), p.A181E) |  
          | ISCN | - |  
          | DB-ID | TNFRSF13B_000009 See all 7 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) | 0.00544 View details |  
          | Owner | VKGL-NL_Leiden |  
          | Database submission license | Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International   |  
          | Created by | VKGL-NL_Leiden |  
          | Date created | 2024-04-19 20:27:30 +02:00 (CEST) |  
          | Date last edited | N/A |   
 
 
 
       
 
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