Table 3.

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  
−33G to A3-150 None  1  1  
−9/−10GG to AT3-150 None 3 (1 homozygous)  0  
127G to A3-151 Ala25 to Thr  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  
Nucleotide Change Amino Acid Change MI (n = 104)Controls (n = 104)
−133C to A3-150 None  1  
−33G to A3-150 None  1  1  
−9/−10GG to AT3-150 None 3 (1 homozygous)  0  
127G to A3-151 Ala25 to Thr  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  
F3-150

Ireland et al.20 

F3-151

Doggen et al.21 

F3-152

Neutral polymorphism.

F3-153

This study.

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