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    | Variant #0000657397 (NC_000014.8:g.23883022G>A, NM_000257.2:c.5736C>T (MYH7))
        
          | 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.23883022G>A |  
          | DNA change (hg38) | g.23413813G>A |  
          | Published as | MYH7(NM_000257.2):c.5736C>T (p.(Ile1912=), p.I1912=), MYH7(NM_000257.4):c.5736C>T (p.I1912=) |  
          | ISCN | - |  
          | DB-ID | MYH7_000423 See all 4 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) | 0.00063 View details |  
          | Owner | VKGL-NL_Utrecht |  
          | Database submission license | Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International   |  
          | Created by | VKGL-NL_Utrecht |  
          | Date created | 2020-03-23 16:13:27 +01:00 (CET) |  
          | Date last edited | 2023-01-11 15:44:22 +01:00 (CET) |   
 
 
 
       
 
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