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    | Variant #0000711835 (NC_000017.10:g.?, NM_014336.3:c.? (AIPL1))
        
          | Chromosome | 17 |  
          | Allele | Parent #1 |  
          | 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.? |  
          | DNA change (hg38) | - |  
          | Published as | AF148864:651G>A (CCG?CCA)  Pro217Pro |  
          | ISCN | - |  
          | DB-ID | MYH2_000008 See all 81 reported entries |  
          | Variant remarks | - |  
          | Reference | PubMed: Sohocki 2001 |  
          | ClinVar ID | - |  
          | dbSNP ID | - |  
          | Origin | CLASSIFICATION record |  
          | Segregation | - |  
          | Frequency | - |  
          | Re-site | - |  
          | VIP | - |  
          | Methylation | - |  
          | Average frequency (gnomAD v.2.1.1) | Genomic location of variant could not be determined |  
          | Owner | Julia Lopez |  
          | Database submission license | Creative Commons Attribution 4.0 International   |  
          | Created by | Julia Lopez |  
          | Date created | 2021-01-14 12:40:33 +01:00 (CET) |  
          | Date last edited | N/A |  
 
 
       
 
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