| Variant #0001039933 (NC_000014.8:g.24709325A>G, NM_001099274.1:c.1166T>C (TINF2))
        
          | Chromosome | 14 |  
          | 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.24709325A>G |  
          | DNA change (hg38) | - |  
          | Published as | TINF2(NM_001099274.1):c.1166T>C (p.I389T), TINF2(NM_001099274.3):c.1166T>C (p.(Ile389Thr)) |  
          | ISCN | - |  
          | DB-ID | GMPR2_000003 See all 3 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) | 0.00013 View details |  
          | Owner | VKGL-NL_Leiden |  
          | Database submission license | Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International   |  
          | Created by | VKGL-NL_Leiden |  
          | Date created | 2025-05-05 21:14:00 +02:00 (CEST) |  
          | Date last edited | N/A |   
 
 
 
       
 
 Variant on transcripts
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