Table 1.
Gene | Alteration | Frequency of alteration % | ||
TCGA* | ICGC(OV-AU)§ | BriTROC-1 | ||
AKT1 | Amplification | 2.9-5.2 | 2.2 | |
Deletion | 0-0.2 | |||
Mutation | 0.3 | 3.3 | ||
AKT2 | Amplification | 5.8-8 | 9.8 | 11.4 |
Deletion | 0.3-1 | |||
Mutation | 3.3 | |||
AKT3 | Amplification | 4.1-9.5 | 4.3 | |
Deletion | 0.2-0.4 | |||
Mutation | 1 | 7.6 | ||
PIK3CA | Amplification | 18-29 | 22.8 | |
Mutation | 1 | 2.2 | 4.6 | |
PIK3CB | Amplification | 3.9-11.4 | 13.0 | |
Mutation | 0.3 | 1.1 | 2.3 | |
PIK3R1 | Amplification | 0-0.2 | ||
Deletion | 2-3.5 | |||
Mutation | 2 | 2.2 | ||
PTEN | Amplification | 0.7-1.2 | ||
Deletion | 4.5-6.1 | 2.2 | ||
Mutation | 1 | 6.5 | ||
RICTOR | Amplification | 3.5-7.1 | 3.3 | 9.1 |
Mutation | 1.1 |
Mutation types include missense mutations, truncating mutations or fusion. *TCGA studies accessed via cBioPortal; data presented involve the range of 3 studies. §ICGC OV-AU cohort accessed via https://icgc.org/4cV. BriTROC-1 data accessed via[63].