Table 3.

Mutation spectrum for patients with NRAS-mutant AML and who have the CYP1A1*2B (Val) allele

KaryotypeCYP1A1 alleleMutation: codon-base substitution/
amino acid change
5q/7q Ile/Val 12.2 G → A/Gly → Asp  
5q/7q Ile/Val 12.2 G → A/Gly → Asp 
5q/7q Ile/Val 61.1 C → A/Gln → Lys 
5q/7q Val/Val 12.2 G → A/Gly → Asp 
3q Ile/Val 12.1 G → A/Gly → Ser 
3q Val/Val 12.2 G → C/Gly → Ala 
+8 Ile/Val 33.3 T → G/Asp → Glu 
t(15;17) Ile/Val 12.1 G → A/Gly → Ser 
KaryotypeCYP1A1 alleleMutation: codon-base substitution/
amino acid change
5q/7q Ile/Val 12.2 G → A/Gly → Asp  
5q/7q Ile/Val 12.2 G → A/Gly → Asp 
5q/7q Ile/Val 61.1 C → A/Gln → Lys 
5q/7q Val/Val 12.2 G → A/Gly → Asp 
3q Ile/Val 12.1 G → A/Gly → Ser 
3q Val/Val 12.2 G → C/Gly → Ala 
+8 Ile/Val 33.3 T → G/Asp → Glu 
t(15;17) Ile/Val 12.1 G → A/Gly → Ser 
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