Mutation Details for c.489+31C>G

cDNA Name c.489+31C>G 
Exon or Intron intron 4 
Legacy Exon or Intron intron 4 
Legacy Name 621+31C/G 
Other Details This polymorphism was seen in a Pakistani individual with no known family history of cystic fibrosis. 
Contributors Andrew N, Malone G, Schwarz M   1999-09-02
Institute Royal Manchester Children's Hospital, England 
Submitted Phenotype Details  
Reference Andrew et al. 1999 

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The Database was last updated at Apr 25, 2011