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    | Variant #0000961457 (NC_000002.11:g.179398515C>T, NM_001267550.1:c.102827G>A (TTN))
        
          | Chromosome | 2 |  
          | 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.179398515C>T |  
          | DNA change (hg38) | - |  
          | Published as | TTN(NM_001256850.1):c.97904G>A (p.(Arg32635Gln)), TTN(NM_001267550.2):c.102827G>A (p.R34276Q), TTN(NM_133432.3):c.76007G>A (p.R25336Q) |  
          | ISCN | - |  
          | DB-ID | TTN_001151 See all 5 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) | 3.0E-5 View details |  
          | Owner | VKGL-NL_Groningen |  
          | Database submission license | Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International   |  
          | Created by | VKGL-NL_Groningen |  
          | Date created | 2024-02-26 20:06:56 +01:00 (CET) |  
          | Date last edited | N/A |   
 
 
 
       
 
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