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. 2023 Jun 9;13:1153131. doi: 10.3389/fonc.2023.1153131

Table 2.

The post-transformation gene mutations of NGS in the 10 patients.

Gene
(Mutation point)
Patients (Mutation abundance (%))
Patient 1 Patient 2 Patient 3 Patient 4 Patient 5 Patient 6 Patient 7 Patient 8 Patient 9 Patient 10
EGFR Exon 19 del Exon 19 del Exon 21 L858R Exon 19 del Exon 21 L858R Exon 19 del Exon 21 L858R Exon 19 del Exon 21 L858R
T790M ✓(12.4%) ✓(17.6%)
RB1 loss ✓(9.2%) ✓(6.5%) ✓(13.4%) ✓(15.2%) ✓(5.7%) ✓(7.4%) ✓(13.7%)
TP53 ✓ (p.A159D) (8.4%) ✓(p.R273H)(13.7%) ✓(p.R273H) (20.3%) ✓(p.A159D) (17.8%) ✓(p.A159D) (5.9%) ✓(p.A159D) (7.6%) ✓(p.R273H) (13.4%) ✓(p.R273H) (22.8%) ✓(p.A159D) (14.6%)
MYC amplification ✓(28.4%)
NF1 (p.R461T) ✓(22.5%)
PIK3CA (p.E545K)  ✓(4.6%)
PTEN loss ✓(16.8%)
CCNE1 (Exon7, c.476A > G) ✓(8.9%)
CDK6 amplification ✓(14.2%)
BRAF (p.D594G) ✓ (5.6%)

✓ indicating the presence of gene mutation, ✘ indicating the absence of gene mutation.