Table 2.
The specific mutational information of six MRD-positive HCC patients.
| ID | Gene | Chromosome | Exon | c.dot | p.dot | frequency | Variant Type |
|---|---|---|---|---|---|---|---|
| 69168 | CREBBP | chr16 | Exon31+1424 | c.6596A>T | p.Q2199L | 0.003217 | Substitution |
| 69168 | EZH2 | chr7 | Exon10-30 | c.1209_1211del | p.E404del | 0.00552 | Deletion |
| 69168 | TP53 | chr17 | Exon5+1 | c.376T>G | p.Y126D | 0.003066 | Substitution |
| 79060 | TP53 | chr17 | Exon6+48 | c.607G>A | p.V203M | 0.002152 | Substitution |
| 52813 | NF1 | chr17 | Exon47-68 | c.6995C>G | p.S2332* | 0.005093 | Substitution |
| 63144 | EZH2 | chr7 | Exon2-56 | c.62C>G | p.S21* | 0.003297 | Substitution |
| 63144 | GLI3 | chr7 | Exon15+1996 | c.4427del | p.N1476Tfs*12 | 0.003307 | Deletion |
| 63144 | NF1 | chr17 | Exon3-13 | c.276del | p.K92Nfs*11 | 0.003922 | Deletion |
| 65536 | APC | chr5 | Exon16-3556 | c.7090del | p.M2364Cfs*10 | 0.003487 | Deletion |
| 65536 | GLI3 | chr7 | Exon15+1996 | c.4427del | p.N1476Tfs*12 | 0.003692 | Deletion |
| 92916 | TERT | chr5 | c.-124C>T | 0.010394 | Substitution | ||
| 92916 | TP53 | chr17 | Exon7-36 | c.747G>T | p.R249S | 0.010289 | Substitution |
| 92916 | TP53 | chr17 | IVS3-2 | c.97-2A>T | 0.00618 | Substitution |
HCC, hepatocellular carcinoma; MRD, minimal residual disease.