VCL non-truncating variants in DCM cohorts


The table below lists the 9 rare (MAF<0.0001 in ExAC) non-truncating VCL variants identified in a cohort of 590 DCM patients. When this rare variant frequency of 0.01525 is compared with a background population rate of 0.00984, there is a case excess of 0.00541, although this is not statistically significant for non-truncating VCL variants in DCM (p=0.2024).


Variant Type:      All protein-altering variants     -     Truncating variants     -     Non-Truncating variants
Source:      LMM



No. Variant (CDS) Variant (Protein) Variant Type Cases (590)LMM class ExAC frequency
1. c.2444A>G p.K815Rmissense 1VUS favour pathogenic (1)0.000016
2. c.3092G>A p.R1031Qmissense 1VUS (1)0.000000
3. c.952C>T p.R318Cmissense 1VUS (1)0.000024
4. c.3226C>T p.R1076Wmissense 1VUS (1)0.000015
5. c.2862_2864delGTT inframe 1VUS favour pathogenic (1)0.000000
6. c.2852C>G p.P951Rmissense 1Likely Benign (1)0.000008
7. c.1390A>C p.K464Qmissense 1VUS (1)0.000000
8. c.1844C>T p.A615Vmissense 1VUS (1)0.000024
9. c.3373C>T p.R1125Cmissense 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.