Mutation Details for c.2645G>A

cDNA Name c.2645G>A 
Protein Name p.Trp882X 
Exon or Intron exon 16 
Legacy Exon or Intron exon 14b 
Legacy Name W882X 
Other Details The above mutation was found on one CF chromosome in a patient of Belgian origin by DGGE screening and DNA sequencing. 
Contributors Férec C, Mercier B, Quere I, Lissens W, Bonduelle M, Liebaers   1995-07-26
Institute Centre de Transfusion Sanguine et de Biogénétique, Brest, France 
Submitted Phenotype Details The mutation was found in a carrier for CF. No clinical data available.(pers.corr. Ferec) 
Reference Férec et al (NL#67) 

To check if there are any papers published about this mutation/variant on PubMed, please click here.

Comments or questions? Please email to cftr.admin
The Database was last updated at Apr 25, 2011