Table 2. Somatic mutations in known cancer genes.
Sample | Gene | Mutation | Frequency |
---|---|---|---|
1 | EP300 | p.G1777C | 0.06 |
2 | DNMT3A | p.Y533C | 0.185 |
3 | EZH2 | p.A483S | 0.46 |
TP53 | p.M169I | 0.029 | |
4 | BCOR | p.P1156L | 0.49 |
EPHA7 | p.G592S | 0.14 | |
WT1 | p.T278I | 0.11 | |
TET2 | p.Q1702* | 0.06 | |
EGFR | p.A871E | 0.042 | |
5 | ALK | p.R1209Q | 0.21 |
ETV6 | p.P25S | 0.038 | |
6 | NOTCH2 | p.P1101T | 0.18 |
NF1 | p.Q2434H | 0.099 | |
SMARCA4 | p.D694E | 0.087 | |
12 | TET2 | p.E1874K | 0.17 |
Mutations listed in this table were identified by targeted sequencing with an allele frequency of ⩾10%. Mutations occurring at a lower frequency were included if previously reported in COSMIC.