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. 2018 Apr 27;9(32):22749–22768. doi: 10.18632/oncotarget.25229

Table 3. Alterations detected in Colon cancer (CC) patients (n=31).

Patient SNV Allele
Frequency
Validation (Sequencing) CNA Validation (RT-PCR) Fusion
CC1 BRAF-V600E 32% Sanger
CC2 MTOR-T1977K
KRAS-G12D
7,5%
16%
CC3
CC4 KRAS-A146T 8% FGFR1 (5) Yes
CC5 KRAS-G12C 14%
CC6 PIK3CA-E542K
KRAS-G12V
30%
49%
Sanger
Sanger
CC7 PIK3CA-H1047R
BRAF-V600E
23%
22.5%
Sanger
CC8 PIK3CA-G1049C
BRAF-V600E
20%
19%
Sanger
Sanger
CC9
CC10
CC11 KRAS-A146T 44.5%
CC12 NRAS-G61K 25%
CC13 NGS Panel**
CC14
CC15
CC16 PIK3CA-H1047Y
BRAF-V600E
16.5%
9%
CC17 KRAS-G12S
PIK3CA-E542K
37.5%
39%
CC18 KRAS-G12V 37.5%
CC19 KRAS-A146T 57%
CC20
CC21 NGS Panel
CC22
CC23
CC24 KRAS-G12V
PIK3CA-E545K
31%
39%
CC25 KRAS-G13D 15%
CC26 KRAS-G12A
ERBB3-G332K
15%
5.5%
CC27
CC28 KRAS-G12S
EGFR-G719D
NRAS-G61K
33%
10%
38%
Sanger
CC29 KRAS-G13D
PIK3CA-E545K
31%
36%
CC30 RET-A883V
KRAS-G12D
AKT1-E17K
9%
37%
11%
CC31 KRAS-G13D
KRAS-A146T
10%
38%

** The NGS Panel used is the Comprehensive Cancer Panel from Thermofisher.