Summary of mutations identified in TM gene in patients with myocardial infarction
Nucleotide Change . | Amino Acid Change . | MI (n = 104) . | Controls (n = 104) . |
---|---|---|---|
−133C to A3-150 | None | 1 | 0 |
−33G to A3-150 | None | 1 | 1 |
−9/−10GG to AT3-150 | None | 3 (1 homozygous) | 0 |
127G to A3-151 | Ala25 to Thr | 2 | 0 |
682G to A | (Pro 209) None | 1 | 0 |
1418C to T3-152 | Ala455 to Val | 18 (3 homozygous) | 18 (3 homozygous) |
insT 16893-153 | Sequence changes from Ala 546 | 1 | 0 |
Nucleotide Change . | Amino Acid Change . | MI (n = 104) . | Controls (n = 104) . |
---|---|---|---|
−133C to A3-150 | None | 1 | 0 |
−33G to A3-150 | None | 1 | 1 |
−9/−10GG to AT3-150 | None | 3 (1 homozygous) | 0 |
127G to A3-151 | Ala25 to Thr | 2 | 0 |
682G to A | (Pro 209) None | 1 | 0 |
1418C to T3-152 | Ala455 to Val | 18 (3 homozygous) | 18 (3 homozygous) |
insT 16893-153 | Sequence changes from Ala 546 | 1 | 0 |