Fig. 4
From: Targeted sequencing reveals complex, phenotype-correlated genotypes in cystic fibrosis
Missense substitutions and in-frame deletions/insertions annotated in accordance with used variant databases and computational tools. VUS stands for Variant of Uncertain Significance; D – pathogenic; N – benign/non CF-causing; U – annotation could not be assessed; VVS – variant of varying clinical significance according to CFRT2 variant classification