Table III.
# | Sample ID | Pathological diagnosis | Gene | Mutation AA | Ion PGM Variant Frequency (%) | Sanger result Consistent? |
---|---|---|---|---|---|---|
1 | 7 | ESCC | TP53 | p.R175H | 47.01 | YES |
2 | 39 | EAC | TP53 | p.A159V | 30.53 | YES |
3 | 34 | EAC | TP53 | p.C176F | 39.57 | YES |
4 | 3 | ESCC | TP53 | p.R175H | 35.16 | YES |
5 | 49 | ESCC | TP53 | p.H179R | 20.20 | YES |
6 | 33 | EAC | PIK3CA | p.E542K | 11.14 | YES |
7 | 45 | ESCC | TP53 | p.R342* | 66.92 | YES |
8 | 47 | ESCC | TP53 | p.C275Y | 12.92 | YES |
9 | 8 | ESCC | TP53 | p.R342* | 14.4 | YES |
Nonsense mutations resulting in STOP codon; EAC: esophageal adenocarcinoma; ESCC: esophageal squamous cell carcinoma.