Roche assay: | |
---|---|
Amplicon | Mutations |
exon 4 | R117H,621+1G → T |
exon 7 | R334W, R347P |
exon 9 | A455E, 5/7/9T polymorphism |
exon 10 | Δ1507, ΔF508. F508C, I507V, I506V polymorphism |
exon 11 | 1717-1G → A, G542X, S549N, G551D, R553X, R560T |
exon 20 | W1282X |
exon 21 | N1303K |
intron 19 | 3849+10kb C → T |
Innogenetics assay: | |
exon 3 | 394delTT, G85E, E60X |
exon/intron 4 | 621+1G-T, R117H |
exon 7 | 1078delT, R347P, R334W |
exon 13 | 2143delT, 2183AA-G, 2184delA |
exon 19 | R1162X, 3659delC |
intron 5 | 711+5G-A |
intron8/exon 9 | A455E,, 5T,7T,9T |
intron 14b | 2789+5G-A |
intron 19 | 3849+10kb C-T |