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. 2017 Jul 22;8(41):69888–69905. doi: 10.18632/oncotarget.19435

Table 4. Somatic mutations in each subtype.

Somatic mutations EBV (N=7) MSI (N=19) CIN (N=46) GS (N=35) P value
Cases (%) Cases (%) Cases (%) Cases (%)
TP53 0 0.0% 5 26.3% 26 56.5% 10 28.6% 0.003a
ACVR1B 0 0.0% 1 5.3% 1 2.2% 0 0.0% 0.534
ALK 0 0.0% 3 15.8% 2 4.3% 1 2.9% 0.232
APC 2 28.6% 1 5.3% 8 17.4% 1 2.9% 0.050
ARID1A 4 57.1% 14 73.7% 12 26.1% 9 25.7% 0.000a
BCOR 1 14.3% 9 47.4% 2 4.3% 0 0.0% 0.016a
BRAF 0 0.0% 3 15.8% 0 0.0% 0 0.0% 0.003a
CBWD1 0 0.0% 0 0.0% 1 2.2% 1 2.9% 1.000
CCND1 0 0.0% 3 15.8% 2 4.3% 2 5.7% 0.323
CD274 1 14.3% 0 0.0% 0 0.0% 0 0.0% 0.065
CDH1 3 42.9% 1 5.3% 3 6.5% 4 11.4% 0.052
CIC 0 0.0% 5 26.3% 3 6.5% 2 5.7% 0.082
CR1 0 0.0% 5 26.3% 2 4.3% 8 22.9% 0.220
CTNNB1 1 14.3% 2 10.5% 0 0.0% 2 5.7% 0.054
EGFR 0 0.0% 4 21.1% 0 0.0% 1 2.9% 0.005a
ERBB2 0 0.0% 5 26.3% 2 4.3% 1 2.9% 0.028a
ERBB3 0 0.0% 5 26.3% 2 4.3% 2 5.7% 0.049a
FBXW7 0 0.0% 3 15.8% 3 6.5% 1 2.9% 0.301
FGFR2 0 0.0% 2 10.5% 0 0.0% 0 0.0% 0.057
HLA-B 0 0.0% 3 15.8% 2 4.3% 0 0.0% 0.088
IRF2 0 0.0% 2 10.5% 1 2.2% 1 2.9% 0.429
JAK2 0 0.0% 1 5.3% 1 2.2% 0 0.0% 0.534
KDR 0 0.0% 3 15.8% 1 2.2% 0 0.0% 0.046a
KRAS 0 0.0% 5 26.3% 1 2.2% 0 0.0% 0.002a
LARP4B 0 0.0% 3 15.8% 1 2.2% 0 0.0% 0.046a
MDM2 0 0.0% 1 5.3% 0 0.0% 0 0.0% 0.243
MEDAG 0 0.0% 2 10.5% 0 0.0% 0 0.0% 0.057
MLH1 0 0.0% 2 10.5% 0 0.0% 0 0.0% 0.057
MSH2 0 0.0% 4 21.1% 1 2.2% 0 0.0% 0.009a
MTOR 0 0.0% 3 15.8% 3 6.5% 0 0.0% 0.111
MVK 0 0.0% 4 21.1% 0 0.0% 0 0.0% 0.002a
MYC 1 14.3% 0 0.0% 0 0.0% 0 0.0% 0.065
PGM5 1 14.3% 4 21.1% 0 0.0% 0 0.0% 0.001a
PIK3CA 2 28.6% 7 36.8% 1 2.2% 0 0.0% 0.000a
PTEN 0 0.0% 2 10.5% 0 0.0% 1 2.9% 0.096
RHOA 2 28.6% 1 5.3% 2 4.3% 4 11.4% 0.139
SMAD4 0 0.0% 1 5.3% 1 2.2% 0 0.0% 0.534
STK11 0 0.0% 1 5.3% 1 2.2% 0 0.0% 0.534
ZBTB20 0 0.0% 5 26.3% 0 0.0% 0 0.0% 0.000a
Mutation rate 2.6 6.6 1.8 1.5

ap value less than 0.05.

Abbreviations: CIN, chromosomal instability, EBV, Epstein-Barr virus; GS, genomically stable; MSI, microsatellite instability. Fisher`s exact test was performed to evaluate differences in the respective proportions of somatic mutations between subgroups.