Mutation Details for c.869+5g>A

cDNA Name c.869+5g>A 
Exon or Intron intron 7 
Other Details  
Contributors and Institutes
Altieri JP - Laboratoire de Génétique Moléculaire, IURC 641, Av. du Doyen Gaston Giraud 34093 Montpellier Cedex 5, France
Guittard C - Laboratoire de Génétique Moléculaire, IURC 641, Av. du Doyen Gaston Giraud 34093 Montpellier Cedex 5, France
Templin C - Laboratoire de Génétique Moléculaire, IURC 641, Av. du Doyen Gaston Giraud 34093 Montpellier Cedex 5, France
Claustres M - Laboratoire de Génétique Moléculaire, IURC 641, Av. du Doyen Gaston Giraud 34093 Montpellier Cedex 5, France
des Georges M - Laboratoire de Génétique Moléculaire, IURC 641, Av. du Doyen Gaston Giraud 34093 Montpellier Cedex 5, France
  
Submitted Phenotype Details This mutation was identified by sequencing in a newborn presenting positive IRT at birth (104ng/ml - IRT normal value < 65 ng/ml) and carrying p.F508del on the other allele. The sweat test was borderline at birth (48/45 mmol/l). At 5 yo., he is pancreatic sufficient and no symptoms of classical CF  
Reference  

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