JUP variants in DCM cohorts


The table below lists the 2 rare (MAF<0.0001 in ExAC) protein-altering JUP variants identified in a cohort of 425 DCM patients (304 patients from OMGL, 121 patients from LMM). As the background population rate of rare protein-altering JUP variants (0.01196) is greater than this case frequency (0.00471), there is no excess of variants in this DCM patient cohort, suggesting that protein-altering JUP variants are not causative for DCM.


Variant Type:      All protein-altering variants     -     Truncating variants     -     Non-Truncating variants
Source:      Combined (OMGL + LMM)     -     OMGL     -     LMM



No. Variant (CDS) Variant (Protein) Variant Type Cases (425)OMGL classLMM class ExAC frequency
1. c.578T>C p.M193Tmissense 1VUS (1)0.000043
2. c.1129C>A p.R377Smissense 1VUS (1)0.000024

References

1. Roddy Walsh, Kate L. Thomson, James S. Ware, Birgit H. Funke, Jessica Woodley, Karen J. McGuire, Francesco Mazzarotto, Edward Blair, Anneke Seller, Jenny C. Taylor, Eric V. Minikel, Exome Aggregation Consortium, Daniel G. MacArthur, Martin Farrall, Stuart A. Cook and Hugh Watkins. Reassessment of Mendelian gene pathogenicity using 7,855 cardiomyopathy cases and 60,706 reference samples. Genet Med. 2016 doi:10.1038/gim.2016.90.

2. Pugh TJ, Kelly MA, Gowrisankar S, Hynes E, Seidman MA, Baxter SM, Bowser M, Harrison B, Aaron D, Mahanta LM, Lakdawala NK, McDermott G, White ET, Rehm HL, Lebo M, Funke BH. The landscape of genetic variation in dilated cardiomyopathy as surveyed by clinical DNA sequencing. Genet Med. 2014 Aug;16(8):601-8.