Mutation Details for c.2620-17g>T

cDNA Name c.2620-17g>T 
Exon or Intron intron 15 
Other Details  
Contributors and Institutes error reading database  
Submitted Phenotype Details This probable polymorphism was identified by direct sequencing in a CBAVD patient who was compound heterozygous for 2 CFTR mutations.  

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