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. 2018 Nov 6;20(12):1219–1226. doi: 10.1016/j.neo.2018.10.004

Table 2.

Frequency of Breakdown of RAS and BRAF Mutations Detected in Colorectal Cancer Patients

Mutation Status No. of Cases Proportion Among 302 Cases
WT RAS or BRAF 142 47.0%
KRAS exon 2 mutant 113 37.4%
 p.G12S 5 1.7%
 p.G12C 8 2.6%
 p.G12R 4 1.3%
 p.G12D 44 14.6%
 p.G12 V 23 7.6%
 p.G12A 6 2.0%
 p.G12A, p.G12R 1 0.3%
 p.G13D 20 6.6%
 p.G12D, p.G13D 2 0.7%
 Other KRAS exon 2 mutant* 0 0.0%
KRAS exon 3 mutant 6 2.0%
 p.A59E 1 0.3%
 p.Q61H 5 1.7%
 Other KRAS exon 3 mutant* 0 0.0%
KRAS exon 4 mutant 10 3.3%
 p.K117N 2 0.7%
 p.A146T 6 2.0%
 p.A146P 1 0.3%
 p.A146V 1 0.3%
NRAS exon 2 mutant 6 2.0%
 p.G12D 4 1.3%
 p.G12V 2 0.7%
 Other NRAS exon 2 mutants 0 0.0%
NRAS exon 3 mutant 8 2.6%
 p.Q61K 2 0.7%
 p.Q61L 5 1.7%
 p.Q61R 1 0.3%
 Other NRAS exon 3 mutant 0 0.0%
NRAS exon 4 mutant 0 0.0%
BRAF V600E mutant 18 6.0%

*KRAS p.G13S, p.G13R, p.G13V, and p.G13A.

**KRAS p.A59T, p.A59G, p.Q61K, p.Q61E, p.Q61L, p.Q61P, and p.Q61R.

§RAS p.G12S, pG12C, p.G12R, and p.G12A.

NRAS p.A59T, p.A59G, pQ61E, p.Q61P, and Q61H.

NRAS p.K117N, p.A146T, p.A146P, and p.A146V.