Mutation Details for c.3368-44G>A
|
|
cDNA Name
|
c.3368-44G>A
|
|
Exon or Intron
|
intron 20
|
|
Legacy Exon or Intron
|
intron 17b
|
|
|
3500-44G/A
|
|
Other Details
|
The intron 17b variant was only observed once in an individual suspected to have CF.
|
|
Contributors
|
Dörk T,
El-Harith E-H A,
Schmidtke J,
Stuhrmann M
1996-11-21
|
|
Institute
|
Institut fur Humangenetik,
Medizinische Hachschule Hannover,
Hannover, Germany
|
|
Submitted Phenotype Details
|
|
|
Reference
|
Dörk et al. (NL#69)
|
To check if there are any papers published about this mutation/variant on PubMed, please click here.
|
|
|
|
|
