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    | Variant #0000556722 (NC_000016.9:g.15797967T>A, NM_001040113.1:c.*22A>T (MYH11))
        
          | Chromosome | 16 |  
          | 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.15797967T>A |  
          | DNA change (hg38) | g.15704110T>A |  
          | Published as | MYH11(NM_001040113.1):c.*22A>T (p.(=)), MYH11(NM_001040114.1):c.5821A>T (p.T1941S), MYH11(NM_002474.3):c.5800A>T (p.T1934S) |  
          | ISCN | - |  
          | DB-ID | MYH11_000006 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) | 0.00137 View details |  
          | Owner | VKGL-NL_Leiden |  
          | Database submission license | Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International   |  
          | Created by | VKGL-NL_Leiden |  
          | Date created | 2019-07-18 18:22:55 +02:00 (CEST) |  
          | Date last edited | 2024-08-28 13:16:32 +02:00 (CEST) |   
 
 
 
       
 
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