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. 2020 May 4;126(14):3219–3228. doi: 10.1002/cncr.32876

Table 2.

Key Oncogene Mutation Spectrum

Oncogene Mutation No. a % b Oncogene Mutation No. a % b
EGFR driver mutations, n = 1418 mutations in 1361 patients c     ERBB2 mutations, n = 126 mutations in 124 patients    
Exon 19 deletions 705 51.8 Exon 20 insertion 76 61.3
L858R 468 34.4 S310F, S310Y 16 12.9
G719A, G719C, G719D, G719R, G719S 66 4.8 V659E 7 5.6
Exon 20 insertion 61 4.5 L755P, L755S, L755A 6 4.8
L861Q, L861R 38 2.8 V777L 4 3.2
S768I 19 1.4 V842I 3 2.4
L833V 9 0.7 D769Y, D769D 3 2.4
Others 52 3.8 Others 11 8.9
KRAS mutations, n = 910 mutations in 888 patients c     ALK fusions, n = 65    
G12C, G12V, G12D, G12A, G12S, G12F, G12R, G12E 716 80.6 EML4‐ALK fusion 58 89.2
G13C, G13D, G13E, G13F, G13P, G13R, G13V 72 8.1 STRN‐ALK fusion 3 4.6
Q61H, Q61L, Q61R, Q61K 72 8.1 KLC1‐ALK fusion 2 3.1
V14I 10 1.1 KIF5B‐ALK fusion 1 1.5
A146V, A146T, A146P 10 1.1 TFG‐ALK fusion 1 1.5
Others 30 3.4      
BRAF mutations, n = 142 mutations in 139 patients     ROS1 fusions, n = 9 mutations    
V600E, V600K 56 40.3 CD74‐ROS1 fusion 5 55.6
G469A, G469V, G469R, G469E 31 22.3 EZR‐ROS1 fusion 2 22.2
G466V, G466R, G466A 12 8.6 SDC4‐ROS1 fusion 1 11.1
N581S 11 7.9 TPM3‐ROS1 fusion 1 11.1
K601E 7 5.0 RET fusions, n = 45    
D594G, D594A 5 3.6 KIF5B‐RET fusion 28 62.2
G596R, G596 4 2.9 CCDC6‐RET fusion 13 28.9
Others 16 11.5 NCOA4‐RET fusion 4 8.9
a

No. indicates the number of mutations identified.

b

The percentage (%) indicates the proportion of patients with a mutation in that gene who had the respective mutation.

c

Double mutation profiles are detailed in Supporting Tables 6 and 8.