Mutation Details for c.592G>A

cDNA Name c.592G>A 
Protein Name p.Ala198Thr 
Exon or Intron exon 6 
Legacy Exon or Intron exon 6a 
Legacy Name A198T 
Other Details  
Contributors E. Rohlfs  
Institute  
Submitted Phenotype Details suspected diagnosis of CF 
Reference not published 

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