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

Table 4. Alterations detected in Rectal cancer (RC) patients (n=25).

Patient SNV Allele
Frequency
Validation (Sequencing) CNA Validation (RT-PCR) Fusion
RC1 ND NGS Panel**
RC2 ND NGS Panel** FGFR1 (7.5) Yes
RC3 ND
RC4 ND
RC5 ND
RC6 BRAF-V600E 10% Sanger
RC7 KRAS-A146P 16%
RC8 KRAS-G12V 41% Sanger
RC9 ND
RC10 ND
RC11 ND
RC12 ND
RC13 KRAS-A146T
ERBB2-S310F
47%
40%
RC14 KRAS-G13D 15.5% Sanger
RC15 ND
RC16 ND
RC17 ND
RC18 KRAS-G12V
PIK3CA-E545K
EGFR-A289D
27%
19%
6%
Sanger
Sanger
*
RC19 KRAS-G13D
AKT1-E17K
23%
13%
RC2 ND
RC21 ND
RC22 KRAS-G12V 38%
RC23 ND
RC24 KRAS-G12S
PIK3CA-E545K
24%
12%
Sanger
Sanger
RC25 ND

* SNV not confirmed by Sanger sequencing.

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