A discarded synonymous variant in <i>NPHP3</i> explains nephronophthisis and congenital hepatic fibrosis in several families
Eric Olinger, Intisar Al Alawi, Mohammed S. Al Riyami, Issa Al Salmi, Elisa Molinari, Eissa Faqeih, Mohamed H. Al‐Hamed, Miguel Barroso‐Gil, Laura Powell, Abdulrahman Al‐Hussaini, Khawla A. Rahim, Naif A. M. Almontashiri, Colin G. Miles, Shirlee Shril, Friedhelm Hildebrandt, Ian Wilson, John A. Sayer
Abstract
Half of patients with a ciliopathy syndrome remain unsolved after initial analysis of whole exome sequencing (WES) data, highlighting the need for improved variant filtering and annotation. By candidate gene curation of WES data, combined with homozygosity mapping, we detected a homozygous predicted synonymous allele in NPHP3 in two children with hepatorenal fibrocystic disease from a consanguineous family. Analyses on patient-derived RNA shows activation of a cryptic mid-exon splice donor leading to frameshift. Remarkably, the same rare variant was detected in four additional families with hepatorenal disease from UK, US, and Saudi patient cohorts and in addition, another synonymous NPHP3 variant was identified in an unsolved case from the Genomics England 100,000 Genomes data set. We conclude that synonymous NPHP3 variants, not reported before and discarded by pathogenicity pipelines, solved several families with a ciliopathy syndrome. These findings prompt careful reassessment of synonymous variants, especially if they are rare and located in candidate genes.