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

Table 2. Alterations detected in Gastric cancer (GC) patients (n=22).

Patient SNV Allele
Frequency
Validation (Sequencing) CNA Validation (RT-PCR) Fusion
G1 ND
G2 ND ERRB2 (CN=5.29)
MYC (CN=8.5)
Yes
G3 ND
G4 ND CDK6 (CN=56.13)
ERBB2 (CN=39.92)
CCND1 (CN=7)
Yes
G5 KRAS-G12V 21% Sanger N.E.
G6 ND CCND1 (CN=4.88) Yes
G7 ND
G8 ND N.E.
G9 KRAS-G12D 29% Sanger
G10 PIK3CA-E546R
MAP2K1-L57T
8%
5%
Sanger
*
G11 PIK3CA-E545L 6%
G12 ND
G13 PIK3CA-M1043I
ERBB2-R896C
JAK3-R657G
18%
12%
5%
* CCND1 (CN=6.5)
MYC (CN=6.5)
Yes
G14 ND N.E.
G15 ND ERBB2 (CN=10.62) Yes
G16 ND
G17 ND N.E.
G18 ND
G19 EGFR-A289D
ERBB2-R896C
9%
18%
G20 PIK3CA-H1047R
PIK3CA-H1048Y
JAK3-R657G
24%
58%
4%


*
G21 PIK3CA-E547K
KIT-D816N
SMO-R290H
ERBB3-E332K
62%
2%
100%
80%
Sanger
*
Sanger
N.E.
G22 NRAS-A146T
NRAS-G61L
KRAS-G13S
5%
42%
13%
Sanger N.E.

N.E. – Non Evaluable.

* SNV not confirmed Sanger sequencing.