| Variation name (cDNA level) | Variation name (protein level) | Variation status | Variation class |
| c.3937C>T | p.Gln1313X | Heterozygous | Mutation |
| wt codon | wt aa | mutant codon | mutant aa | mutational event | mutation type |
| CAA | Gln | TAA | Stop | C->T | Ts |
| Structure | Key Residue (HCD) | Pyrimidin doublet | CpG |
| NBD2 | Yes, coding strand | No |
| Mutation(s) on the other allele: c.1521_1523delCTT (p.Phe508del) |
| At the mRNA level | On restriction map |
| New restriction site(s): Mse I Lost restriction site(s): Bcl I, Dpn I, Dpn II, Mbo I, Sau3A I |
| Sample ID | Patient status | Gender | Transmission | Age of onset | Age of death | Geographic origin |
| FR001-00056-00008 | Proband | Female | Autosomal recessive |
| Phenotypic group | Disease |
| CF |
| Reference ID | Reference |
| 1 | Unpublished data |