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.
| No. | Variant (CDS)▼ | Variant (Protein) | Variant Type▼ | Cases (355)▼ | OMGL class | ExAC frequency |
|---|---|---|---|---|---|---|
| 1. | c.337C>G | p.L113V | missense | 1 | Likely Pathogenic | 0.000000 |
| 2. | c.368G>C | p.S123T | missense | 1 | VUS | 0.000000 |
| 3. | c.688G>A | p.D230N | missense | 1 | Pathogenic | 0.000000 |
| 4. | c.695T>G | p.L232R | missense | 1 | VUS | 0.000000 |
| 5. | c.359C>T | p.A120V | missense | 1 | VUS | 0.000000 |
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.
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