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. Author manuscript; available in PMC: 2017 Jul 10.
Published in final edited form as: Cancer Cell. 2016 Jan 21;29(2):229–240. doi: 10.1016/j.ccell.2015.12.012

Table 2.

Significantly (q < 0.1) Mutated Genes in Ampullary Carcinomas (n = 172)

Gene Frequency (%) Patients Number of inactivating alteration p value q value
1 KRAS 47.7 82 0 1.14E-118 1.06E-116
2 TP53 55.8 96 30 5.88E-117 2.73E-115
3 CTNNB1 23.3 40 1 2.71E-22 8.40E-21
4 SMAD4 16.3 28 10 4.37E-16 1.02E-14
5 APC 33.7 58 54 1.89E-14 3.52E-13
6 ELF3 12.2 21 17 1.15E-11 1.78E-10
7 GNAS 11.6 20 1 5.58E-08 7.41E-07
8 ACVR2A 7.6 13 9 1.34E-05 0.000147192
9 ERBB3 10.5 18 0 1.42E-05 0.000147192
10 ACVR1B 8.1 14 5 4.60E-05 0.000428017
11 ARID2 15.7 27 21 5.68E-05 0.000479964
12 BRAF 9.3 16 0 0.00013007 0.00100804
13 CDKN2A 4.7 8 5 0.000227549 0.00162785
14 TGFBR1 6.4 11 3 0.000609132 0.00404637
15 SOX9 8.1 14 12 0.000876341 0.00543331
16 LOXHD1 11 19 0 0.00128913 0.00749306
17 ERBB2 11.6 20 0 0.00165826 0.00907168
18 FBXW7 5.8 10 3 0.00254902 0.01317
19 EPHA3 7 12 2 0.005577 0.027298
20 EPHA6 5.8 10 0 0.0059163 0.0275108
21 TGFBR2 5.8 10 3 0.0110298 0.0466613
22 RNF43 7 12 9 0.0110381 0.0466613
23 CNTN4 7 12 2 0.0154074 0.0622994
24 SLITRK5 8.1 14 2 0.0255168 0.0988775