The table below lists the 70 rare (MAF<0.0001 in ExAC) non-truncating TTN variants identified in a cohort of 156 DCM patients. When this rare variant frequency of 0.44870 is compared with a background population rate of 0.39200, there is a statistically significant case excess of 0.05670 (p<0.0001), which suggests that approximately of these variants may be pathogenic.
| No. | Variant (CDS)▼ | Variant (Protein) | Variant Type▼ | Cases (156)▼ | LMM class | ExAC frequency |
|---|---|---|---|---|---|---|
| 1. | c.37432C>T | p.P12478S | missense | 2 | VUS | 0.000000 |
| 2. | c.67147G>A | p.G22383R | missense | 1 | VUS | 0.000058 |
| 3. | c.25046C>G | p.A8349G | missense | 1 | VUS | 0.000008 |
| 4. | c.54167G>A | p.R18056Q | missense | 1 | VUS | 0.000026 |
| 5. | c.102428T>C | p.M34143T | missense | 1 | VUS | 0.000074 |
| 6. | c.93968C>T | p.A31323V | missense | 1 | VUS | 0.000057 |
| 7. | c.62780G>A | p.R20927H | missense | 1 | VUS | 0.000008 |
| 8. | c.99434G>A | p.R33145Q | missense | 1 | VUS | 0.000033 |
| 9. | c.6478A>G | p.T2160A | missense | 1 | VUS | 0.000016 |
| 10. | c.20260A>G | p.Lys6754Glu | missense | 1 | VUS | 0.000000 |
| 11. | c.11450G>A | p.G3817D | missense | 1 | VUS | 0.000017 |
| 12. | c.43019T>C | p.I14340T | missense | 1 | VUS | 0.000008 |
| 13. | c.80608C>A | p.Pro26870Thr | missense | 1 | VUS | 0.000000 |
| 14. | c.89947G>A | p.V29983M | missense | 1 | VUS | 0.000099 |
| 15. | c.48395G>A | p.R16132H | missense | 1 | VUS | 0.000066 |
| 16. | c.96140C>T | p.T32047M | missense | 1 | VUS | 0.000057 |
| 17. | c.58982G>A | p.G19661D | missense | 1 | VUS | 0.000016 |
| 18. | c.55139T>C | p.I18380T | missense | 1 | VUS | 0.000050 |
| 19. | c.2605A>T | p.T869S | missense | 1 | VUS | 0.000041 |
| 20. | c.39749_39766delTTGCTCCTGAAGAGGAAA | inframe | 1 | VUS | 0.000000 | |
| 21. | c.9674A>G | p.N3225S | missense | 1 | VUS | 0.000024 |
| 22. | c.68272G>A | p.D22758N | missense | 1 | VUS | 0.000026 |
| 23. | c.78980G>A | p.R26327Q | missense | 1 | VUS | 0.000049 |
| 24. | c.74527A>G | p.N24843D | missense | 1 | VUS | 0.000033 |
| 25. | c.50647C>T | p.Pro16883Ser | missense | 1 | VUS | 0.000000 |
| 26. | c.39163A>G | p.Lys13055Glu | missense | 1 | VUS | 0.000000 |
| 27. | c.91478A>G | p.Glu30493Gly | missense | 1 | VUS | 0.000000 |
| 28. | c.58684A>G | p.Ile19562Val | missense | 1 | VUS | 0.000000 |
| 29. | c.105590G>A | p.G35197D | missense | 1 | VUS | 0.000041 |
| 30. | c.94629A>G | p.I31543M | missense | 1 | VUS | 0.000066 |
| 31. | c.63632T>C | p.Val21211Ala | missense | 1 | VUS | 0.000000 |
| 32. | c.99814C>T | p.L33272F | missense | 1 | VUS | 0.000009 |
| 33. | c.15369_15371delGTT | inframe | 1 | VUS - favor pathogenic | 0.000000 | |
| 34. | c.12037G>A | p.Ala4013Thr | missense | 1 | VUS | 0.000000 |
| 35. | c.6941T>C | p.I2314T | missense | 1 | VUS | 0.000008 |
| 36. | c.5132C>T | p.S1711F | missense | 1 | VUS | 0.000016 |
| 37. | c.20742T>A | p.Phe6914Leu | missense | 1 | VUS | 0.000000 |
| 38. | c.18663A>C | p.E6221D | missense | 1 | VUS | 0.000099 |
| 39. | c.28754A>C | p.Glu9585Ala | missense | 1 | VUS | 0.000000 |
| 40. | c.70181C>T | p.T23394M | missense | 1 | VUS | 0.000024 |
| 41. | c.77816A>C | p.Asp25939Ala | missense | 1 | VUS | 0.000000 |
| 42. | c.22386T>G | p.Asp7462Glu | missense | 1 | VUS | 0.000000 |
| 43. | c.72985A>G | p.Asn24329Asp | missense | 1 | VUS | 0.000000 |
| 44. | c.85195G>A | p.E28399K | missense | 1 | VUS | 0.000016 |
| 45. | c.93472G>C | p.Asp31158His | missense | 1 | VUS | 0.000000 |
| 46. | c.62290G>C | p.Glu20764Gln | missense | 1 | VUS | 0.000000 |
| 47. | c.89766G>C | p.Lys29922Asn | missense | 1 | VUS | 0.000000 |
| 48. | c.57415A>C | p.Ile19139Leu | missense | 1 | VUS | 0.000000 |
| 49. | c.96286G>A | p.A32096T | missense | 1 | VUS | 0.000066 |
| 50. | c.54091A>G | p.S18031G | missense | 1 | VUS | 0.000008 |
| 51. | c.64903C>T | p.R21635C | missense | 1 | VUS | 0.000024 |
| 52. | c.107285G>A | p.R35762Q | missense | 1 | VUS | 0.000033 |
| 53. | c.6029A>G | p.Y2010C | missense | 1 | VUS | 0.000008 |
| 54. | c.3469G>A | p.V1157I | missense | 1 | VUS | 0.000041 |
| 55. | c.11140A>G | p.Ile3714Val | missense | 1 | VUS | 0.000000 |
| 56. | c.5582G>A | p.R1861H | missense | 1 | VUS | 0.000082 |
| 57. | c.72488G>A | p.R24163H | missense | 1 | VUS | 0.000054 |
| 58. | c.26765G>A | p.Arg8922Gln | missense | 1 | VUS | 0.000000 |
| 59. | c.19015T>C | p.Tyr6339His | missense | 1 | VUS | 0.000000 |
| 60. | c.24344G>A | p.S8115N | missense | 1 | VUS | 0.000083 |
| 61. | c.84523T>C | p.Trp28175Arg | missense | 1 | VUS | 0.000000 |
| 62. | c.98296G>T | p.D32766Y | missense | 1 | VUS | 0.000008 |
| 63. | c.47887A>G | p.M15963V | missense | 1 | VUS | 0.000033 |
| 64. | c.58705G>A | p.D19569N | missense | 1 | VUS | 0.000017 |
| 65. | c.105630A>C | p.Gln35210His | missense | 1 | VUS | 0.000000 |
| 66. | c.98243G>A | p.R32748H | missense | 1 | VUS | 0.000066 |
| 67. | c.54685G>A | p.V18229M | missense | 1 | VUS | 0.000091 |
| 68. | c.102638A>G | p.N34213S | missense | 1 | VUS | 0.000008 |
| 69. | c.1186G>A | p.A396T | missense | 1 | VUS | 0.000008 |
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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