TNNT2 non-truncating variants in ExAC

TNNT2 gene summary
TNNT2 variants in DCM, HCM

The table below lists the TNNT2 non-truncating variants found in the ExAC population database with a mean allelic frequency (MAF) less than 0.0001, classified for this study as a rare variant. Click on each variant for more details, including presence in the 1000 Genomes and Exome Sequencing Project databases, a breakdown by ethnic class and the variant's role in inherited cardiac disease. Use the form below to customise the variant selection. The table can be sorted by variant location, variant type or ExAC frequency.




No. Genomic coord.✝ Variant (CDS)▼ Variant (Protein) Variant Type▼ ExAC frequency▼Populations*
1. 201328348 c.857G>A p.R286H missense 0.00007882●●●●●●
2. 201328352 c.853G>A p.G285R missense 0.00006641●●●●●●
3. 201335991 c.178A>G p.M60V missense 0.00004946●●●●●●
4. 201337317 c.106G>C p.A36P missense 0.00004945●●●●●●
5. 201333455 c.430C>T p.R144W missense 0.00003481●●●●●●
6. 201334772 c.230C>T p.P77L missense 0.00003396●●●●●●
7. 201337341 c.82G>A p.A28T missense 0.00003301●●●●●●
8. 201331078 c.652G>T p.V218L missense 0.00003295●●●●●●
9. 201328372 c.833G>A p.R278H missense 0.00002144●●●●●●
10. 201328790 c.782T>C p.I261T missense 0.00001914●●●●●●
11. 201328778 c.794G>A p.R265Q missense 0.00001813●●●●●●
12. 201333454 c.431G>A p.R144Q missense 0.00001743●●●●●●
13. 201328767 c.805A>G p.N269D missense 0.00001732●●●●●●
14. 201328764 c.808G>T p.D270Y missense 0.00001717●●●●●●
15. 201334784 c.218A>G p.N73S missense 0.00001707●●●●●●
16. 201334778 c.224T>G p.V75G missense 0.00001702●●●●●●
17. 201334767 c.235A>T p.I79F missense 0.00001695●●●●●●
18. 201337343 c.80C>G p.A27G missense 0.00001651●●●●●●
19. 201331143 c.587G>A p.R196Q missense 0.00001648●●●●●●
20. 201337308 c.115G>A p.E39K missense 0.00001648●●●●●●
21. 201331147 c.583G>A p.E195K missense 0.00001648●●●●●●
22. 201334417 c.283A>G p.M95V missense 0.00001648●●●●●●
23. 201335969 c.200C>T p.P67L missense 0.00001648●●●●●●
24. 201330438 c.749T>A p.L250Q missense 0.00001647●●●●●●
25. 201342373 c.10A>C p.I4L missense 0.00001647●●●●●●
26. 201342343 c.40G>A p.E14K missense 0.00001647●●●●●●
27. 201330442 c.745G>A p.D249N missense 0.00001647●●●●●●
28. 201328342 c.863A>G p.K288R missense 0.00001146●●●●●●
29. 201328348 c.857G>T p.R286L missense 0.00001126●●●●●●
30. 201328349 c.856C>T p.R286C missense 0.00001119●●●●●●
31. 201328370 c.835G>A p.G279R missense 0.00001072●●●●●●
32. 201333433 c.452G>A p.R151H missense 0.00000907●●●●●●
33. 201333436 c.449A>G p.N150S missense 0.00000897●●●●●●
34. 201334796 c.206C>T p.S69L missense 0.00000868●●●●●●
35. 201333460 c.425A>G p.N142S missense 0.00000865●●●●●●
36. 201333494 c.391C>T p.R131W missense 0.00000864●●●●●●
37. 201333484 c.401G>A p.R134Q missense 0.00000862●●●●●●
38. 201333477 c.408G>T p.E136D missense 0.00000862●●●●●●
39. 201333467 c.418A>G p.I140V missense 0.00000862●●●●●●
40. 201333479 c.406G>C p.E136Q missense 0.00000861●●●●●●
41. 201333479 c.406G>A p.E136K missense 0.00000861●●●●●●
42. 201334745 c.257A>C p.D86A missense 0.00000850●●●●●●
43. 201341163 c.59C>T p.A20V missense 0.00000828●●●●●●
44. 201337332 c.91G>A p.D31N missense 0.00000825●●●●●●
45. 201337343 c.80C>A p.A27E missense 0.00000825●●●●●●
46. 201337340 c.83C>A p.A28E missense 0.00000825●●●●●●
47. 201331090 c.640G>A p.E214K missense 0.00000824●●●●●●
48. 201336923 c.145G>C p.E49Q missense 0.00000824●●●●●●
49. 201342379 c.4T>C p.S2P missense 0.00000824●●●●●●
50. 201334342 c.358C>G p.L120V missense 0.00000824●●●●●●
51. 201332466 c.528G>C p.K176N missense 0.00000824●●●●●●
52. 201341155 c.67G>A p.E23K missense 0.00000824●●●●●●
53. 201335970 c.199C>A p.P67T missense 0.00000824●●●●●●
54. 201330487 c.700A>G p.K234E missense 0.00000824●●●●●●
55. 201332441 c.553G>T p.G185W missense 0.00000824●●●●●●
56. 201334426 c.274C>T p.R92W missense 0.00000824●●●●●●
57. 201334416 c.284T>C p.M95T missense 0.00000824●●●●●●
58. 201332506 c.488A>G p.E163G missense 0.00000824●●●●●●
59. 201330438 c.749T>C p.L250P missense 0.00000824●●●●●●
60. 201336921 c.147_149delAGA p.Glu51del inframe 0.00000824●●●●●●
61. 201336904 c.164C>A p.A55D missense 0.00000824●●●●●●
62. 201334326 c.374A>G p.D125G missense 0.00000824●●●●●●
63. 201332447 c.547C>T p.H183Y missense 0.00000824●●●●●●
64. 201334389 c.311C>T p.A104V missense 0.00000824●●●●●●
65. 201332471 c.523A>C p.K175Q missense 0.00000824●●●●●●
66. 201331101 c.629A>T p.K210M missense 0.00000824●●●●●●
67. 201332527 c.467G>A p.R156K missense 0.00000824●●●●●●
68. 201342349 c.34G>A p.E12K missense 0.00000824●●●●●●
69. 201330453 c.734C>T p.A245V missense 0.00000824●●●●●●
70. 201337322 c.101C>T p.A34V missense 0.00000824●●●●●●
71. 201336918 c.150G>T p.E50D missense 0.00000824●●●●●●
72. 201334327 c.373G>A p.D125N missense 0.00000824●●●●●●
73. 201332448 c.546G>A p.M182I missense 0.00000824●●●●●●

* This highlights the relative frequency of the variant in the ExAC populations - Non-Finnish European, African, East Asian, South Asian, American and Finnish. Higher frequencies are denoted by darker shades of green, variants absent in a population are coloured light gray.

✝ Genomic coordinates refer to the GRCh37 release of the human genome.