DSP variants in DCM cohorts


The table below lists the 9 rare (MAF<0.0001 in ExAC) protein-altering DSP variants identified in a cohort of 123 DCM patients. When this rare variant frequency of 0.07317 is compared with a background population rate of 0.03148, there is a statistically significant case excess of 0.04169 (p<0.0001), which suggests that approximately 5 of these variants may be pathogenic.


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 (123)LMM class ExAC frequency
1. c.943C>T p.R315Cmissense 2VUS0.000074
2. c.8495G>T p.G2832Vmissense 1VUS0.000008
3. c.607G>A p.D203Nmissense 1VUS0.000000
4. c.8481_8492del p.Ser2843_Arg2846delinframe 1VUS0.000000
5. c.699G>A p.W233Xnonsense 1Likely Pathogenic0.000000
6. c.939+1G>A essential splice site 1Likely Pathogenic0.000000
7. c.6885A>T p.Q2295Hmissense 1VUS0.000000
8. c.2848dupA frameshift 1Likely Pathogenic0.000000

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.