CDNK1B (p27) mutations in BRAFV600E-mutant classical HCL
| Sample identifier . | BRAF mutation . | CDKN1B mutation . |
|---|---|---|
| P0001 | c.1799T>A; (p.V600E) | c.500delC, (p.A167QfsX37) |
| P0013 | c.1799T>A; (p.V600E) | c.180G>A, (p.W60*) |
| c.238G>C; (p.E80Q) | ||
| P0621 | c.1799T>A; (p.V600E) | c.333-353del21; p.G111del6 |
| P0774 | c.1799T>A; (p.V600E) | c.475+1G>A; (splice acceptor variant) |
| P0806 | c.1799T>A; (p.V600E) | c.475+1G>T; (splice acceptor variant); c.596A>C; (p.X199S) |
| P0811 | c.1799T>A (p.V600E) | c.281C>T; (p.P94L)# |
| P0911 | c.1799T>A; (p.V600E) | c.5C>G; p.S2* |
| c.58C>T; p.Q20* | ||
| c.475+1G>T; (splice acceptor variant) | ||
| P0912 | c.1799T>A; (p.V600E) | c.87C>A; (p.C29*) |
| P0914 | c.1799T>A; (p.V600E) | c.179G>A; (p.W60*) |
| P0919 | c.1799T>A; (p.V600E) | c.475+1G>T; (splice acceptor variant) |
| P0941 | c.1799T>A; (p.V600E) | c.227G>A; (p.W76*) |
| P0897 | c.1799T>A; (p.V600E) | c.596A>C; (p.X199S) |
| P0902 | c.1799T>A; (p.V600E) | c.228G>A; (p.W76*) |
| Sample identifier . | BRAF mutation . | CDKN1B mutation . |
|---|---|---|
| P0001 | c.1799T>A; (p.V600E) | c.500delC, (p.A167QfsX37) |
| P0013 | c.1799T>A; (p.V600E) | c.180G>A, (p.W60*) |
| c.238G>C; (p.E80Q) | ||
| P0621 | c.1799T>A; (p.V600E) | c.333-353del21; p.G111del6 |
| P0774 | c.1799T>A; (p.V600E) | c.475+1G>A; (splice acceptor variant) |
| P0806 | c.1799T>A; (p.V600E) | c.475+1G>T; (splice acceptor variant); c.596A>C; (p.X199S) |
| P0811 | c.1799T>A (p.V600E) | c.281C>T; (p.P94L)# |
| P0911 | c.1799T>A; (p.V600E) | c.5C>G; p.S2* |
| c.58C>T; p.Q20* | ||
| c.475+1G>T; (splice acceptor variant) | ||
| P0912 | c.1799T>A; (p.V600E) | c.87C>A; (p.C29*) |
| P0914 | c.1799T>A; (p.V600E) | c.179G>A; (p.W60*) |
| P0919 | c.1799T>A; (p.V600E) | c.475+1G>T; (splice acceptor variant) |
| P0941 | c.1799T>A; (p.V600E) | c.227G>A; (p.W76*) |
| P0897 | c.1799T>A; (p.V600E) | c.596A>C; (p.X199S) |
| P0902 | c.1799T>A; (p.V600E) | c.228G>A; (p.W76*) |