Table 3.
Patient no. | Cancer type | Tumor stage | Position | Gene | Mutation (amino acid change) | Mutation type | % Mutation: tumor (reads) | % Mutation: plasma (reads) | % Mutation: WBC (reads) |
---|---|---|---|---|---|---|---|---|---|
48 | UKN | IV | chr7:55241708 | EGFR | p.G719A | SNP | 0.0 (3528) | 3.4 (22307) | 0.0 (190) |
chr7:55242511 | EGFR | p.D761Y | SNP | 0.0 (1000) | 3.5 (21853) | 0.0 (310) | |||
chr12:25398285 | KRAS | p.G12C | SNP | 0.0 (2529) | 4.8 (17379) | 0.0 (312) | |||
chr12:25398281 | KRAS | p.G13D | SNP | 0.0 (2536) | 3.6 (17465) | 0.0 (313) | |||
75 | AC | IIIA | chr7:55249071 | EGFR | p.T790M | SNP | 0.0 (2845) | 2.8 (9887) | 0.0 (1106) |
chr12:25398284 | KRAS | p.G12V | SNP | 0.0 (19015) | 1.1 (14689) | 0.0 (7065) | |||
78 | AC | IIIA | chr7:55249071 | EGFR | p.T790M | SNP | 0.0 (130) | 21.5 (10975) | 0.0 (244) |
90 | AC | IIIA | chr17:7577538 | TP53 | Intronic | SNP | 0.0 (7432) | 9.5 (86317) | 0.0 (7353) |
114 | SCC | IIIA | chr7:140453136 | BRAF | p.V600E | SNP | 0.0 (7669) | 43.1 (17175) | 0.0 (3180) |
chr7:55241708 | EGFR | p.G719A | SNP | 0.0 (10692) | 59.6 (91440) | 0.0 (4044) | |||
chr7:55242464 | EGFR | p.745_749del | DEL | 0.0 (11397) | 60.4 (77443) | 0.0 (4330) | |||
chr7:55242511 | EGFR | p.D761Y | SNP | 0.0 (11386) | 61.6 (76946) | 0.0 (4321) | |||
chr7:55249005 | EGFR | p.S768I | SNP | 0.0 (4691) | 4.3 (10185) | 0.0 (2257) | |||
chr7:55249012 | EGFR | p.D770delinsDG | INS | 0.1 (4688) | 3.9 (9952) | 0.1 (2257) | |||
chr12:25398285 | KRAS | p.G12C | SNP | 0.0 (14166) | 66.6 (58977) | 0.0 (5117) | |||
chr12:25398281 | KRAS | p.G13D | SNP | 0.0 (14211) | 65.0 (59150) | 0.0 (5138) | |||
chr3:178936091 | PIK3CA | p.E545K | SNP | 0.0 (13901) | 51.4 (42929) | 0.0 (5936) | |||
118 | AC | IV | chr7:55242511 | EGFR | p.D761N | SNP | 0.0 (10264) | 1.1 (9481) | 0.0 (8745) |
chr3:178936091 | PIK3CA | p.E545K | SNP | 0.0 (8801) | 1.2 (19609) | 0.0 (5406) | |||
123 | AC | IIIA | chr7:55241708 | EGFR | p.G719D | SNP | 0.0 (9315) | 1.1 (26694) | 0.0 (13761) |
chr7:55242511 | EGFR | p.D761N | SNP | 0.0 (13069) | 1.0 (21772) | 0.0 (19806) | |||
chr12:25398281 | KRAS | p.G13V | SNP | 0.0 (16150) | 1.0 (17697) | 0.0 (17816) | |||
139 | AC | IIIB | chr7:55249063 | EGFR | p.Q787Q | SNP | 0.3 (5833) | 4.1 (5984) | 0.0 (4334) |
SCC: squamous cell carcinoma; AC: adenocarcinoma; UKN: unknown; SNP: single nucleotide polymorphism; DEL: deletion; INS: insert.