MYH7 non-truncating variants in HCM cohorts


The table below lists the 434 rare (MAF<0.0001 in ExAC) non-truncating MYH7 variants identified in a cohort of 3200 HCM patients. When this rare variant frequency of 0.13562 is compared with a background population rate of 0.01350, there is a statistically significant case excess of 0.12212 (p<0.0001), which suggests that approximately 391 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 (3200)OMGL class ExAC frequency
1. c.2389G>A p.A797Tmissense 24Pathogenic0.000032
2. c.1988G>A p.R663Hmissense 17Pathogenic0.000016
3. c.2609G>A p.R870Hmissense 13Pathogenic0.000000
4. c.1816G>A p.V606Mmissense 13Pathogenic0.000000
5. c.1063G>A p.A355Tmissense 10Likely Pathogenic0.000000
6. c.1357C>T p.R453Cmissense 10Pathogenic0.000000
7. c.2539A>G p.K847Emissense 10Likely Pathogenic0.000000
8. c.2348G>A p.R783Hmissense 8Likely Pathogenic0.000016
9. c.5135G>A p.R1712Qmissense 8VUS0.000008
10. c.2221G>T p.G741Wmissense 8Pathogenic0.000000
11. c.2681A>G p.E894Gmissense 7Likely Pathogenic0.000000
12. c.2717A>G p.D906Gmissense 7Likely Pathogenic0.000000
13. c.1207C>T p.R403Wmissense 6Pathogenic0.000000
14. c.3158G>A p.R1053Qmissense 6Likely Pathogenic0.000074
15. c.2207T>C p.I736Tmissense 6Pathogenic0.000000
16. c.4135G>A p.A1379Tmissense 5Pathogenic0.000000
17. c.1142C>A p.A381Dmissense 5Likely Pathogenic0.000000
18. c.4066G>A p.E1356Kmissense 5Likely Pathogenic0.000000
19. c.2722C>G p.L908Vmissense 5Pathogenic0.000000
20. c.2770G>A p.E924Kmissense 5Pathogenic0.000000
21. c.4130C>T p.T1377Mmissense 5VUS0.000000
22. c.2155C>T p.R719Wmissense 5Pathogenic0.000000
23. c.3475G>A p.V1159Mmissense 4VUS0.000000
24. c.958G>A p.V320Mmissense 4VUS0.000008
25. c.2167C>T p.R723Cmissense 4Pathogenic0.000024
26. c.508G>A p.E170Kmissense 4Pathogenic0.000000
27. c.1208G>A p.R403Qmissense 4Pathogenic0.000000
28. c.343T>C p.Y115Hmissense 4Likely Pathogenic0.000008
29. c.1063G>T p.A355Smissense 3VUS0.000000
30. c.715G>A p.D239Nmissense 3Likely Pathogenic0.000000
31. c.2779G>A p.E927Kmissense 3VUS0.000000
32. c.1856C>T p.T619Imissense 3VUS0.000033
33. c.746G>A p.R249Qmissense 3Pathogenic0.000000
34. c.1370T>C p.I457Tmissense 3Likely Pathogenic0.000008
35. c.2631G>C p.M877Imissense 3VUS0.000000
36. c.1279C>A p.L427Mmissense 3Likely Pathogenic0.000000
37. c.2302G>A p.G768Rmissense 3Likely Pathogenic0.000000
38. c.611G>A p.R204Hmissense 3VUS0.000000
39. c.1268C>T p.A423Vmissense 2VUS0.000000
40. c.4124A>G p.Y1375Cmissense 2VUS0.000000
41. c.2572C>T p.R858Cmissense 2VUS0.000000
42. c.2011C>T p.R671Cmissense 2Likely Pathogenic0.000000
43. c.2536G>C p.E846Qmissense 2VUS0.000000
44. c.1405G>A p.D469Nmissense 2VUS0.000008
45. c.1045A>G p.M349Vmissense 2VUS0.000024
46. c.428G>A p.R143Qmissense 2Likely Pathogenic0.000008
47. c.1433T>A p.I478Nmissense 2Likely Pathogenic0.000000
48. c.1318G>A p.V440Mmissense 2VUS0.000000
49. c.1447G>A p.E483Kmissense 2Pathogenic0.000008
50. c.2220G>T p.K740Nmissense 2Likely Pathogenic0.000000
51. c.5329G>A p.A1777Tmissense 2VUS0.000041
52. c.427C>T p.R143Wmissense 2Likely Pathogenic0.000049
53. c.1051A>G p.K351Emissense 2Likely Pathogenic0.000000
54. c.641G>A p.G214Dmissense 2Likely Pathogenic0.000000
55. c.5561C>T p.T1854Mmissense 2VUS0.000033
56. c.578A>G p.Q193Rmissense 2Likely Pathogenic0.000000
57. c.1231G>A p.V411Imissense 2Likely Pathogenic0.000008
58. c.1324C>T p.R442Cmissense 2Likely Pathogenic0.000008
59. c.1182C>A p.D394Emissense 2VUS0.000000
60. c.4259G>T p.R1420Lmissense 2VUS0.000000
61. c.2359C>T p.R787Cmissense 2Likely Pathogenic0.000057
62. c.1954A>G p.R652Gmissense 2Likely Pathogenic0.000008
63. c.767G>A p.G256Emissense 2Likely Pathogenic0.000000
64. c.976G>C p.A326Pmissense 2Likely Pathogenic0.000067
65. c.2881C>G p.L961Vmissense 1VUS0.000000
66. c.4985G>A p.R1662Hmissense 1VUS0.000057
67. c.4418A>G p.E1473Gmissense 1VUS0.000000
68. c.4048G>A p.E1350Kmissense 1VUS0.000000
69. c.3325A>G p.K1109Emissense 1VUS0.000000
70. c.5380C>A p.Q1794Kmissense 1VUS0.000000
71. c.5291T>A p.M1764Kmissense 1VUS0.000000
72. c.4259G>A p.R1420Qmissense 1VUS0.000000
73. c.3593A>G p.D1198Gmissense 1VUS0.000000
74. c.3170G>A p.G1057Dmissense 1VUS0.000000
75. c.2631G>A p.M877Imissense 1VUS0.000000
76. c.3637G>A p.V1213Mmissense 1VUS0.000000
77. c.2906A>C p.H969Pmissense 1VUS0.000000
78. c.2791_2793delGAG inframe 1Likely Pathogenic0.000000
79. c.1579C>A p.P527Tmissense 1VUS0.000000
80. c.2770G>C p.E924Qmissense 1VUS0.000000
81. c.1345A>T p.T449Smissense 1Likely Pathogenic0.000000
82. c.710G>A p.R237Qmissense 1VUS0.000000
83. c.3046A>G p.K1016Emissense 1VUS0.000008
84. c.2389G>C p.A797Pmissense 1Likely Pathogenic0.000000
85. c.2296A>C p.K766Qmissense 1Likely Pathogenic0.000000
86. c.2167C>G p.R723Gmissense 1Pathogenic0.000000
87. c.1759G>A p.D587Nmissense 1Likely Pathogenic0.000000
88. c.1216G>A p.V406Mmissense 1Likely Pathogenic0.000000
89. c.2081G>A p.R694Hmissense 1Likely Pathogenic0.000000
90. c.809A>G p.K270Rmissense 1VUS0.000000
91. c.3373G>C p.E1125Qmissense 1VUS0.000000
92. c.5587C>T p.R1863Wmissense 1VUS0.000008
93. c.5690G>A p.R1897Hmissense 1VUS0.000000
94. c.3899A>T p.Q1300Lmissense 1VUS0.000000
95. c.610C>T p.R204Cmissense 1Likely Pathogenic0.000024
96. c.5029C>T p.R1677Cmissense 1VUS0.000016
97. c.4636G>C p.E1546Qmissense 1VUS0.000000
98. c.3231T>G p.D1077Emissense 1VUS0.000000
99. c.1804A>T p.N602Ymissense 1VUS0.000000
100. c.2683C>A p.Q895Kmissense 1VUS0.000000
101. c.4787C>T p.S1596Lmissense 1VUS0.000041
102. c.2711G>A p.R904Hmissense 1VUS0.000000
103. c.3493A>G p.K1165Emissense 1VUS0.000012
104. c.500C>T p.T167Imissense 1VUS0.000000
105. c.2602G>C p.A868Pmissense 1VUS0.000000
106. c.737A>T p.K246Imissense 1Likely Pathogenic0.000000
107. c.3134G>T p.R1045Lmissense 1VUS0.000016
108. c.2353A>G p.I785Vmissense 1VUS0.000000
109. c.2546T>C p.M849Tmissense 1Likely Pathogenic0.000000
110. c.595G>A p.A199Tmissense 1VUS0.000000
111. c.2183C>T p.A728Vmissense 1VUS0.000000
112. c.2129C>A p.P710Hmissense 1Likely Pathogenic0.000000
113. c.4664A>G p.E1555Gmissense 1VUS0.000000
114. c.788T>C p.I263Tmissense 1Pathogenic0.000000
115. c.5704G>C p.E1902Qmissense 1VUS0.000074
116. c.298G>A p.A100Tmissense 1VUS0.000016
117. c.4132G>C p.D1378Hmissense 1VUS0.000000
118. c.619A>C p.K207Qmissense 1Likely Pathogenic0.000000
119. c.4258C>T p.R1420Wmissense 1VUS0.000008
120. c.3548T>A p.L1183Qmissense 1VUS0.000000
121. c.2707G>C p.E903Qmissense 1VUS0.000000
122. c.4954G>T p.D1652Ymissense 1VUS0.000024
123. c.4343A>G p.N1448Smissense 1VUS0.000000
124. c.4030C>T p.R1344Wmissense 1VUS0.000016
125. c.3289G>A p.E1097Kmissense 1VUS0.000000
126. c.2788G>A p.E930Kmissense 1Likely Pathogenic0.000000
127. c.1479G>A p.M493Imissense 1Likely Pathogenic0.000000
128. c.904C>A p.L302Mmissense 1VUS0.000000
129. c.2606G>T p.R869Lmissense 1VUS0.000000
130. c.1228T>G p.Y410Dmissense 1Likely Pathogenic0.000000
131. c.3622G>A p.D1208Nmissense 1VUS0.000000
132. c.2894A>G p.E965Gmissense 1VUS0.000000
133. c.2555T>C p.M852Tmissense 1Likely Pathogenic0.000000
134. c.694A>C p.N232Hmissense 1Likely Pathogenic0.000000
135. c.2680G>A p.E894Kmissense 1VUS0.000000
136. c.964T>A p.S322Tmissense 1VUS0.000000
137. c.1544T>C p.M515Tmissense 1Pathogenic0.000000
138. c.2471T>C p.V824Amissense 1VUS0.000000
139. c.2156G>A p.R719Qmissense 1Pathogenic0.000000
140. c.1208G>T p.R403Lmissense 1Pathogenic0.000000
141. c.983A>G p.E328Gmissense 1Likely Pathogenic0.000000
142. c.1757T>C p.V586Amissense 1Likely Pathogenic0.000000
143. c.5740G>A p.E1914Kmissense 1VUS0.000000
144. c.5172C>G p.I1724Mmissense 1VUS0.000000
145. c.799C>G p.L267Vmissense 1Likely Pathogenic0.000000
146. c.3341G>A p.R1114Hmissense 1VUS0.000000
147. c.5471A>G p.N1824Smissense 1VUS0.000000
148. c.4276G>A p.E1426Kmissense 1VUS0.000000
149. c.3803G>C p.R1268Pmissense 1VUS0.000000
150. c.5002A>G p.K1668Emissense 1VUS0.000000
151. c.4532A>C p.D1511Amissense 1VUS0.000000
152. c.3208G>A p.E1070Kmissense 1VUS0.000008
153. c.3974C>T p.A1325Vmissense 1VUS0.000026
154. c.3064A>G p.K1022Emissense 1VUS0.000000
155. c.1753A>T p.I585Fmissense 1VUS0.000000
156. c.3428T>G p.L1143Rmissense 1VUS0.000000
157. c.2573G>A p.R858Hmissense 1Likely Pathogenic0.000008
158. c.731T>G p.F244Cmissense 1Likely Pathogenic0.000000
159. c.3133C>T p.R1045Cmissense 1Likely Pathogenic0.000016
160. c.2701G>C p.A901Pmissense 1Likely Pathogenic0.000000
161. c.1121A>T p.E374Vmissense 1Likely Pathogenic0.000000
162. c.80A>G p.Q27Rmissense 1VUS0.000000
163. c.2776C>G p.L926Vmissense 1VUS0.000016
164. c.1346C>T p.T449Imissense 1VUS0.000000
165. c.2069T>C p.M690Tmissense 1Likely Pathogenic0.000000
166. c.2606G>A p.R869Hmissense 1Likely Pathogenic0.000032
167. c.2104A>G p.I702Vmissense 1VUS0.000000
168. c.1436A>G p.N479Smissense 1Likely Pathogenic0.000000
169. c.728G>A p.R243Hmissense 1Likely Pathogenic0.000008
170. c.925G>A p.D309Nmissense 1Likely Pathogenic0.000024
171. c.4108C>A p.Q1370Kmissense 1VUS0.000000
172. c.5088G>C p.E1696Dmissense 1VUS0.000024
173. c.4660G>A p.E1554Kmissense 1VUS0.000000
174. c.5647G>A p.E1883Kmissense 1VUS0.000000
175. c.5773C>T p.R1925Cmissense 1VUS0.000000
176. c.2273T>G p.F758Cmissense 1Likely Pathogenic0.000000
177. c.4144C>T p.R1382Wmissense 1VUS0.000000
178. c.3484G>A p.E1162Kmissense 1VUS0.000000
179. c.3346G>A p.E1116Kmissense 1VUS0.000000
180. c.2700T>A p.D900Emissense 1VUS0.000000
181. c.4817G>A p.R1606Hmissense 1VUS0.000049
182. c.4004C>T p.S1335Lmissense 1VUS0.000033
183. c.3229_3240del p.Asp1077_Leu1080delinframe 1VUS0.000000
184. c.5326A>G p.S1776Gmissense 1Likely Pathogenic0.000032
185. c.1207C>G p.R403Gmissense 1Pathogenic0.000000
186. c.3578G>A p.R1193Hmissense 1VUS0.000000
187. c.2785G>A p.E929Kmissense 1Likely Pathogenic0.000000
188. c.1477A>T p.M493Lmissense 1Likely Pathogenic0.000000
189. c.793A>T p.T265Smissense 1VUS0.000000
190. c.3138G>A p.M1046Imissense 1VUS0.000024
191. c.2501T>A p.F834Ymissense 1VUS0.000000
192. c.2623_2625delGAG p.Glu875delinframe 1Likely Pathogenic0.000000
193. c.920C>A p.P307Hmissense 1Pathogenic0.000000
194. c.2738T>C p.I913Tmissense 1VUS0.000000
195. c.2549C>A p.A850Dmissense 1Likely Pathogenic0.000000
196. c.677C>T p.A226Vmissense 1VUS0.000000
197. c.1477A>G p.M493Vmissense 1Likely Pathogenic0.000000
198. c.2221G>A p.G741Rmissense 1Pathogenic0.000000
199. c.1625A>G p.K542Rmissense 1VUS0.000000
200. c.1358G>A p.R453Hmissense 1Likely Pathogenic0.000000
201. c.4919A>G p.Q1640Rmissense 1VUS0.000000
202. c.789A>G p.I263Mmissense 1Likely Pathogenic0.000000
203. c.5725C>T p.R1909Wmissense 1VUS0.000032
204. c.632C>T p.P211Lmissense 1Likely Pathogenic0.000024

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. Alfares AA, Kelly MA, McDermott G, Funke BH, Lebo MS, Baxter SB, Shen J, McLaughlin HM, Clark EH, Babb LJ, Cox SW, DePalma SR, Ho CY, Seidman JG, Seidman CE, Rehm HL. Results of clinical genetic testing of 2,912 probands with hypertrophic cardiomyopathy: expanded panels offer limited additional sensitivity. Genet Med. 2015 Nov;17(11):880-8.