ACTC1 variants in DCM cohorts


The table below lists the 5 rare (MAF<0.0001 in ExAC) protein-altering ACTC1 variants identified in a cohort of 748 DCM patients. When this rare variant frequency of 0.00668 is compared with a background population rate of 0.00064, there is a case excess of 0.00604, although this is not statistically significant for protein-altering ACTC1 variants in DCM (p=0.0011).


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 (748)LMM class ExAC frequency
1. c.355G>C p.E119Qmissense 1VUS0.000000
2. c.616+1G>A essential splice site 1VUS favour pathogenic0.000000
3. c.475G>A p.D159Nmissense 1VUS0.000000
4. c.806T>C p.I269Tmissense 1VUS favour pathogenic0.000000
5. c.7G>C p.D3Hmissense 1VUS0.000000

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.