Mutation Details for c.1068G>A

cDNA Name c.1068G>A 
Protein Name p.Trp356X 
Exon or Intron exon 8 
Legacy Exon or Intron exon 7 
Legacy Name W356X 
Other Details This mutation has been detected in a CF patient and also in one of her parents. The mutation removes an AluI restriction site. 
Contributors Ellis L   1998-07-07
Institute St. James's University Hospital Leeds, UK 
Submitted Phenotype Details  
Reference Ellis (NL#70) 

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The Database was last updated at Apr 25, 2011