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    | Variant #0000016688 (NC_000014.8:g.23282154A>G, NM_001126105.2:c.454T>C (SLC7A7))
        
          | Chromosome | 14 |  
          | Allele | Parent #1 |  
          | Affects function (as reported) | Affects function |  
          | Affects function (by curator) | Affects function |  
          | Classification method | - |  
          | Clinical classification | pathogenic |  
          | DNA change (genomic) (Relative to hg19 / GRCh37) | g.23282154A>G |  
          | DNA change (hg38) | g.22812945A>G |  
          | Published as | from the first methionine, 453T>C: F152L |  
          | ISCN | - |  
          | DB-ID | SLC7A7_000011 |  
          | Variant remarks | 1 Greek LPI patient (com-het); Functional studies: mutated protein showed moderately reduced transport activity |  
          | Reference | PubMed: Sperandeo 2005 |  
          | ClinVar ID | - |  
          | dbSNP ID | - |  
          | Origin | SUMMARY record |  
          | Segregation | yes |  
          | Frequency | - |  
          | Re-site | - |  
          | VIP | - |  
          | Methylation | - |  
          | Average frequency (gnomAD v.2.1.1) | Retrieve |  
          | Owner | Anne Polvi |  
          | Database submission license | Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International   |  
          | Created by | Anne Polvi |  
          | Date created | 2012-12-04 16:25:21 +01:00 (CET) |  
          | Date last edited | 2017-05-05 18:33:04 +02:00 (CEST) |   
 
 
 
       
 
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