Case number | Concen-tration (ng/ul) | Ladder (bp) | Results | Mutation frequency | Depth |
---|---|---|---|---|---|
1 | 137.8 | 600 | TET2:NM_001127208.2:exon11:c.4662_4663del: p.E1555Vfs*22 TET2:NM_001127208.2:exon8:c.3986T > C:p.L1329P DNMT3A: NM_022552.4:exon16:c.1910T > G:p.L637R DNMT3A: NM_022552.4:exon8:c.928 A > T:p.I310F KMT2B: NM_014727.2:exon28:c.6190G > A:p.V2064M RHOA: NM_001664.4:exon2:c.50G > T:p.G17V | 19% 11% 13% 5% 7% 4% | 149x 73x 141x 268x 220x 135x |
2 | 97.1 | 400 | DNMT3A c.2678G > C:p.W893S TET2 c.1212delG: p.L404fs TET2 c.2286delC: p.H762fs VAV1 c.748 C > T:p.R250C RHOA c.50G > T:p.G17V IDH2 c515G > A:p.R172K TET2 c.3955–2 A > G SETD2 c.2514 2516delCTA: p.S838del | 23% 12% 23% 38% 11% 9% 8% 42% | 100x 76x 158x 143x 210x 124x 89x 156x |
3 | 75.9 | 500 | EP300:NM_001429.4;c.3677T > C;p.11226T NF1;NM_001042492.2;c10161019dup; p.V341Lfs*13 RHOA; NM_001664.4;c.50G > T;p.G17V SIN3A; NM_015477.3;c.974 A > G;p.Y325C STAT3;NM_139276.2;c.1852G > C;p.G618R TET2:NM_001127208.2;c.4618 C > T;p.01540* TET2:NM_001127208.2:c.3581 3587del; p.P1194Lfs*30 | 36% 33% 38% 4% 41% 38% 32% | 130x 178x 165x 230x 126x 134x 200x |
4 | 30.2 | 600 | B2M: NM_004048.3:exon2:c.294T > A:p.Y98* TET2:NM_001127208.2:exon3:c.2272_2273del: p.Q758Dfs*10 TET2:NM_001127208.2:exon11:c.4636 C > T:p.Q1546* TET2:NM_001127208.2:exon9:c.4151 A > G:p.D1384G RHOA: NM_001664.4:exon2:c.50G > T:p.G17V | 22% 21% 19% 5% 16% | 106x 113x 187x 139x 96x |
5 | 149.8 | 100 (unqualified) | Â | Â | Â |
6 | 106.7 | 100 (unqualified) | Â | Â | Â |
7 | 32.3 | 100 (unqualified) | Â | Â | Â |