TPM1 variants in DCM cohorts


The table below lists the 5 rare (MAF<0.0001 in ExAC) protein-altering TPM1 variants identified in a cohort of 355 DCM patients. When this rare variant frequency of 0.01408 is compared with a background population rate of 0.00086, there is a statistically significant case excess of 0.01322 (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 (355)OMGL class ExAC frequency
1. c.368G>C p.S123Tmissense 1VUS0.000000
2. c.688G>A p.D230Nmissense 1Pathogenic0.000000
3. c.695T>G p.L232Rmissense 1VUS0.000000
4. c.359C>T p.A120Vmissense 1VUS0.000000
5. c.337C>G p.L113Vmissense 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.