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Table 3 Summary of genetic alterations in 19 cases of colorectal cancer. Somatic mutations or CNA for the listed genes are shown. Blank indicates wild-type

From: Development and clinical application of an integrative genomic approach to personalized cancer therapy

Patient ID

APC

KRAS

NRAS

BRAF

PIK3CA

PTEN

EGFR

TP53

P0004

p.E763*

p.G12V

  

p.E545K, p.M1043I

   

P0005

p.R554*

p.G12S

     

p.R273H

P0008

   

p.V600E

    

P0009

p.E1309fs*4

     

Gain

p.P151S

P0016

 

p.G12V

  

p.E545K

  

p.R248Q

P0018

p.E1309*, p.V1377fs

p.G13D

     

p.G245S

P0019

p.R232*, p.R1114*

      

p.R333fs*12

P0020

p.T683P, p.R876*, p.E1577*

p.G13D

     

p.F270I

P0022

p.T1493fs*14

      

p.R248Q

P0024

p.E955*

p.N116H,p.Q61P

     

p.S183*

P0025

p.I606fs, p.R1450*

 

p.Q61R

    

p.R273C

P0027

     

Possible loss

 

Mutation in donor splice site

P0028

Splice site donor, p.Q1067*

      

p.R282W

P0031

p.E1097*, p.E1397*

p.G12D

     

p.G245S

P0033

p.E1306*

p.G13D

     

p.R273C

P0034

p.E1322*

p.G12C

     

p.Y220C

P0037

p.R232*

  

p.V600E

 

Splice site acceptor

  

P0043

p.F1354fs, p.S1400*

p.G13D

     

p.C176F

P0046

p.R876*

 

p.G12D

    

p.S127F

Frequency

0.89

0.53

0.11

0.11

0.11

0.11

0.05

0.84