Table 1

 CFTR and SPINK1 sequence variations identified in 30 of the 67 ICP patients

PatientSexCFTR mutationT alleleTG repeatsPSTI mutation
1MΔF508/R117H7/79/10–/–
2WΔF508/A1087P7/910/11–/–
3MΔF508/D1152H7/910/10–/–
4MS1235R/R668C7/711/12–/–
5M2184insA/-7/710/12–/–
6MR31C/-7/710/11–/–
7MR75Q/-7/711/11–/–
8MR347P/-7/711/12–/–
9MS1235R/-7/711/12–/–
10WS1235R/-7/711/12–/–
11MG576A/-7/710/10–/–
12WM348V/-7/910/10–/–
13MV754M/-7/710/11–/–
14M–/–5/711/12–/–
15W–/–5/711/12–/–
16M–/–5/711/12–/–
17W–/–5/911/12–/–
18M–/–5/711/12–/–
19M–/–5/710/10–/–
20W–/–5/710/10–/–
21W–/–5/711/12N34S/-
22W–/–7/710/11N34S/-
23M–/–7/910/11N34S/-
24M–/–7/711/11N34S/-
25M–/–7/711/11N34S/-
26W–/–7/711/11N34S/-
27M–/–7/711/11N34S/-
28W–/–7/710/11N34S/-
29W–/–7/711/11P55S/-
30W–/–7/711/11IVS3+2TC/-