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. Author manuscript; available in PMC: 2015 Oct 13.
Published in final edited form as: Cancer Cell. 2014 Oct 13;26(4):455–464. doi: 10.1016/j.ccell.2014.09.013

Table 2. Fbw7 mutation and homozygous deletion frequency in selected cancers.

Tumor Type No. samples Arginine hotspot mutations Nonsense mutations Other missense mutations All point mutations Arginine hotspot mutations/total point mutations Homozygous deletions (%)
Uterine Carcinosarcoma 56 23% 4% 14% 39% 59% 0%
Colon and rectal adenocarcinoma 212 8% 3% 6% 17% 49% 0%
Uterine corpus endometrial carcinoma 240 6% 3% 8% 16% 37% 0%
Stomach adenocarcinoma 219 5% 2% 2% 9% 59% <1%
Urothelial bladder carcinoma 127 3% 5% 4% 9% 33% 2%
Lung squamous cell carcinoma 178 2% 2% 2% 6% 36% <1%
Head and neck squamous cell carcinoma 302 2% <1% 3% 5% 33% 1%
Cutaneous melanoma 262 <1% 1% 3% 4% 9% <1%
Breast cancer 962 <1% <1% 1% 2% 20% <1%
Cervical squamous adenocarcinoma 36 0% 3% 3% 6% 0% 0%
Lung adenocarcinoma 230 0% 1% <1% 2% 0% 0%
Glioblastoma multiforme 281 0% <1% 0% <1% 0% <1%

Mutation and copy number alteration data were derived from analyses of TCGA data using cBioPortal (Cerami et al., 2012; Gao et al., 2013).