Table 2. Specimens with 10% or lower mutant allele frequencies.
Case | Specimens | Tumor % | mut 1 | mut 1 (%) | mut 2 | mut 2 (%) |
---|---|---|---|---|---|---|
1 | LN/resection | 1–20 | G12D/KRAS | 3.5 | ||
2 | Rectum/resectiona | 31–50b | V344M/PIK3CA | 8.8b | ||
33 | Colon/resection | 31–50b | Q61H/KRAS | 1.95b | ||
67 | Colon/biopsy | 1–20 | E545K/PIK3CA | 7.7 | G12D/KRAS | 17 |
75 | Rectum/resectiona | 1–20 | D594G/BRAF | 7.2 | ||
76 | Colon/resection | 1–20 | Q546H/PIK3CA | 4.1 | G12D/KRAS | 14 |
91 | Colon/resection | 41–60b | E81K/PIK3CA | 8.9b | E545K/PIK3CA | 13b |
98 | Rectum/resectiona | 1–20 | G12A/KRAS | 9.9 | ||
127 | Colon/resection | 51–70b | Q61R/NRAS | 4.0b | H1047R/PIK3CA | 14b |
144 | Colon/biopsy | 41–60b | G15S/KRAS | 8.4b | V600E/BRAF | 29 |
158 | Rectum/resectiona | 1–20 | A59G/KRAS | 5.9 | ||
174 | Colon/biopsy | 1–20 | E542K/PIK3CA | 6.9 | ||
202 | Colon/resection | 61–80b | G12V/KRAS | 5.2b | G13C/NRAS | 36 |
213 | Liver/resectiona | 11–30 | G12D/KRAS | 6.4 | ||
217 | Rectum/resectiona | 1–20 | N345K/PIK3CA | 6.9 | ||
227 | Liver biopsy | 11–30 | V600E/BRAF | 7.5 | ||
270 | Colon/section | 11–30 | E110del/PIK3CA | 9.4 | G13D/KRAS | 17 |
282 | Colon/resection | 61–80b | E545K/PIK3CA | 8.9b | A146T/KRAS | 53 |
287 | Rectum/resectiona | 1–20 | A146T/KRAS | 3.4 | ||
302 | Rectum/resectiona | 31–50b | E545K/PIK3CA | 4.6b |
Abbreviations: mut, mutation; mut 1%, allele frequency of mutation 1; mut 2%, allele frequency of mutation 2; G12A, c.35G4 C; G12D, c.354 G4 A; G12V, C.35G4 T; G13C, c.37G4 T; G13D, c.38G4 A; G15S, c.43G4 A; A59G, c.176C4 G; Q61H, c.183A4 C; Q61R, c.182A4 G; E81K, c.241G4 A; E110del, c.328_330del; A146T, c.436G4 A; V344M, c.1030G4 A; N345K, c.1035T4 A; E542K, c.1624G4 A; E545K, c.1633G4 A; Q546H, c.1638G4 T; D594G, c.1781A4 G; V600E, c.1742A4 G; H1047R, c.3140A4 G
Resection with prior adjuvant therapy.
Mutations with an observed mutant allele frequency at least 10% less than that expected from the estimated tumor cellularity. The expected mutant allele percentage is half of the estimated tumor percentage, assuming heterozygosity with no mutant allele-specific imbalance.