A Classification Model Relative to Splicing for Variants of Unknown Clinical Significance: Application to the CFTR Gene

作者：Raynal Caroline^*; Baux David; Theze Corinne; Bareil Corinne; Taulan Magali; Roux Anne Francoise; Claustres Mireille; Tuffery Giraud Sylvie; Georges Marie des

来源：Human Mutation, 2013, 34(5): 774-784.

DOI：10.1002/humu.22291

• CFTR
• decision flowchart
• VUCS
• interpretation
• splicing

Molecular diagnosis of cystic fibrosis and cystic fibrosis transmembrane regulator (CFTR)-related disorders led to the worldwide identification of nearly 1,900 sequence variations in the CFTR gene that consist mainly of private point mutations and small insertions/deletions. Establishing their effect on the function of the encoded protein and therefore their involvement in the disease is still challenging and directly impacts genetic counseling. In this context, we built a decision tree following the international guidelines for the classification of variants of unknown clinical significance (VUCS) in the CFTR gene specifically focused on their consequences on splicing. We applied general and specific criteria, including comprehensive review of literature and databases, familial genetics data, and thorough in silico studies. This model was tested on 15 intronic and exonic VUCS identified in our cohort. Six variants were classified as probably nonpathogenic considering their impact on splicing and eight as probably pathogenic, which include two apparent missense mutations. We assessed the validity of our method by performing minigenes studies and confirmed that 93% (14/15) were correctly classified. We provide in this study a high-performance method that can play a full role in interpreting the results of molecular diagnosis in emergency context, when functional studies are not achievable.

• 出版日期2013-5