| Variant #0000992276 (NC_000002.11:g.179666894G>C, NM_001267550.1:c.266C>G (TTN))
        
          | Chromosome | 2 |  
          | 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.179666894G>C |  
          | DNA change (hg38) | - |  
          | Published as | TTN(NM_001267550.1):c.266C>G (p.(Ala89Gly)), TTN(NM_001267550.2):c.266C>G (p.A89G) |  
          | ISCN | - |  
          | DB-ID | TTN_005406 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 | 2024-08-28 13:07:21 +02:00 (CEST) |  
          | Date last edited | N/A |   
 
 
 
       
 
 Variant on transcripts
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