Mutation Details for c.273+1G>A

cDNA Name c.273+1G>A 
Exon or Intron intron 3 
Legacy Exon or Intron intron 3 
Legacy Name 405+1G->A 
Other Details This mutation was found in a German PI patient with [delta]F508 on the other allele. The patient carries haplotype C and the rare polymorphism at codon T966.  
Contributors Dork T, Tummler B   1992-08-11
Institute Medizinische Hochschule Hannover Hannova, Germany 
Phenotype Information CFTR2
Reference Dörk et al. 1993e 

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The Database was last updated at Apr 25, 2011