ClinVar

Description

The CFTR c.960A>C; p.Leu320Phe variant is published in the medical literature in one individual with infertility (Morea 2005) and listed in a gene-specific database in an individual with suspected cystic fibrosis (see link below). The variant is not listed in the ClinVar database, but is listed in the dbSNP variant database (rs56093012) and in the Genome Aggregation Database in 3/277024 alleles. Another variant in the same codon, c.958T>G; p.Leu320Val is classified as mildly pathogenic, and found in individuals with CFTR-related disorders (Dorfman 2010, Lucarelli 2010, Masson 2013, Pelletier 2010, Shrijver 2005). The leucine at this position is highly conserved, but computational algorithms (AlignGVGD, PolyPhen2, SIFT) predict this variant is tolerated. Considering available information, there is insufficient evidence to classify this variant with certainty. Link to CFTR L320F in database: http://www.genet.sickkids.on.ca/cftr/MutationDetailPage.external?sp=175 Dorfman R et al. Do common in silico tools predict the clinical consequences of amino-acid substitutions in the CFTR gene? 2010 Clin Genet. 77(5):464-73. Lucarelli M et al. A new complex allele of the CFTR gene partially explains the variable phenotype of the L997F mutation. Genet Med. 2010 12(9):548-55. Masson E et al. A conservative assessment of the major genetic causes of idiopathic chronic pancreatitis: data from a comprehensive analysis of PRSS1, SPINK1, CTRC and CFTR genes in 253 young French patients. 2013 PLoS One. 8(8):e73522. Morea A et al. Gender-sensitive association of CFTR gene mutations and 5T allele emerging from a large survey on infertility. Mol Hum Reprod. 2005 Aug;11(8):607-14. Pelletier A et al. CFTR gene mutation in patients with apparently idiopathic pancreatitis: lack of phenotype-genotype correlation. Pancreatology. 2010 10(2-3):158-64. Schrijver I et al. Diagnostic testing by CFTR gene mutation analysis in a large group of Hispanics: novel mutations and assessment of a population-specific mutation spectrum. J Mol Diagn. 2015 7(2):289-99.