Mutation Details for c.3368-44G>A

cDNA Name c.3368-44G>A 
Exon or Intron intron 20 
Legacy Exon or Intron intron 17b 
Legacy Name 3500-44G/A 
Other Details The intron 17b variant was only observed once in an individual suspected to have CF. 
Contributors Dörk T, El-Harith E-H A, Schmidtke J, Stuhrmann M   1996-11-21
Institute Institut fur Humangenetik, Medizinische Hachschule Hannover, Hannover, Germany 
Submitted Phenotype Details  
Reference Dörk et al. (NL#69) 

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The Database was last updated at Apr 25, 2011