Table 2.
Case | AA Change | SNV | VAF (%) | Mutant Copy Number (per Well) | Total Copy Number (per Well) |
---|---|---|---|---|---|
1 | Y537S | 1610A>C | 0.0025 | 2.8 | 111,150 |
38 | Y537S | 1610A>C | 0.0031 | 3.6 | 116,800 |
49 | Y537S | 1610A>C | 0.0022 | 2.8 | 129,000 |
59 | Y537S | 1610A>C | 0.0028 | 3 | 108,800 |
84 | Y537S | 1610A>C | 0.0018 | 2.8 | 158,000 |
117 | Y537S | 1610A>C | 0.0023 | 2.4 | 106,540 |
119 | Y537S | 1610A>C | 0.0021 | 2.6 | 121,200 |
120 | Y537S | 1610A>C | 0.0024 | 2.6 | 108,500 |
121 | Y537S | 1610A>C | 0.0037 | 3.8 | 102,200 |
139 | Y537S | 1610A>C | 0.1580 | 6.8 | 4304 |
165 | Y537S | 1610A>C | 0.0053 | 2.6 | 48,640 |
173 | Y537S | 1610A>C | 0.0106 | 3 | 28,320 |
177 | Y537S | 1610A>C | 0.0025 | 2.8 | 112,800 |
194 | Y537S | 1610A>C | 0.0026 | 2.6 | 101,700 |
202 | Y537S | 1610A>C | 0.0028 | 2.6 | 91,280 |
132 | Y537S | 1610A>C | 0.0034 | 2.8 | 81,280 |
132 | D538G | 1613A>G | 0.0034 | 2.8 | 81,280 |
2 | D538G | 1613A>G | 0.0041 | 2.6 | 63,840 |
7 | D538G | 1613A>G | 0.0119 | 2.8 | 23,520 |
68 | D538G | 1613A>G | 0.0110 | 4.8 | 43,520 |
144 | D538G | 1613A>G | 0.0422 | 2.8 | 6640 |
145 | D538G | 1613A>G | 0.0060 | 2.8 | 46,690 |
146 | D538G | 1613A>G | 0.0111 | 3 | 27,040 |
158 | D538G | 1613A>G | 0.0053 | 3 | 56,480 |
187 | D538G | 1613A>G | 0.0053 | 2.8 | 52,800 |
207 | D538G | 1613A>G | 0.0111 | 2.6 | 23,520 |
211 | D538G | 1613A>G | 0.0039 | 3.8 | 96,480 |
212 | D538G | 1613A>G | 1.6260 | 36 | 2178 |
AA—amino acid, SNV—single nucleotide variant, and VAF—variant allele frequency.