Mutation Details for c.(?_274)_(489_?)delins41

Note: this mutation was submitted but not yet reviewed by our curator.

cDNA Name c.(?_274)_(489_?)delins41 
Exon or Intron exon 4 
Legacy Exon or Intron exon 4 
Legacy Name CFTRdele4Ins41bp  
Other Details This mutation was identified by QMPSF and Quantitative DHPLC. 
Contributors Marie-Pierre AudrŽzet, Jian-Min Chen, Odile RaguŽns, Karine Giteau, CŽdric Le MarŽchal, Isabelle QuŽrŽ, and Claude FŽrec    2004-06-16
Institute GŽnŽtique MolŽculaire, CHU, Brest, FRANCE  
Submitted Phenotype Details The complex anomaly was identified in a 17 yrs old patient heterozygous for F508del. he is PI and has positive ST  
Reference Genomic Rearrangements in the CFTR gene : Extensive Allelic Heterogeneity and Diverse Mutational Mechanisms Marie-Pierre AudrŽzet, Jian-Min Chen, Odile RaguŽns, Nadia Chuzhanova, Karine Giteau, CŽdric Le MarŽchal, Isabelle QuŽrŽ, David N. Cooper, and Claude FŽrec. Human Mutation (2004), 23:343-357. 

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The Database was last updated at Apr 25, 2011