| Variant #0000804603 (NC_000010.10:g.89623716G>A, NM_000314.4:c.-510G>A (PTEN))
        
          | Chromosome | 10 |  
          | 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.89623716G>A |  
          | DNA change (hg38) | - |  
          | Published as | PTEN(NM_000314.4):c.-510G>A, PTEN(NM_000314.8):c.-511G>A, PTEN(NM_001304717.5):c.10G>A (p.(Gly4Arg), p.G4R) |  
          | ISCN | - |  
          | DB-ID | PTEN_000600 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) | Retrieve |  
          | Owner | VKGL-NL_NKI |  
          | Database submission license | Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International   |  
          | Created by | VKGL-NL_NKI |  
          | Date created | 2021-09-17 14:40:49 +02:00 (CEST) |  
          | Date last edited | 2024-04-19 20:27:30 +02:00 (CEST) |   
 
 
 
       
 
 Variant on transcripts
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