case | Somatic mutations | Copy number variations | |||||
---|---|---|---|---|---|---|---|
STAT5B | TP53 | JAK3 | SETD2 | STAT5A | chromosomal arms | CNV type | |
1 | Â | p.R248Q | p.M511I | Â | p.N642H p.G472S | 8p,8q,9p,12p,20p | deletion |
4q,7q,9q | amplification | ||||||
2 | p.N642H | p.I232Sfs*15 | Â | Â | Â | 4p,4q,7p,10p,10q,15q,18p | deletion |
1q,9q,19q | amplification | ||||||
3 | p.Y665F | p.V147Afs*19 | p.A573V | p.E1772_I1781delinsV p.D2004Ifs*13 | Â | 4p,7p,8p,18p,21q | deletion |
7q,8q,9q,12p,12q,18q,22q | amplification | ||||||
4 | Â | Â | Â | Â | p.Q701L | 6p,7p,18p | deletion |
9q,21q | amplification | ||||||
5 | Â | Â | Â | Â | Â | 7p,8p | deletion |
7q,9q,19q,19p | amplification | ||||||
6 | p.A766V | p.G105C | p.R657Q | Â | Â | 1q,7q,9q,19q,19p | amplification |
7 | p.N642H | Â | Â | p.S1572* | Â | Â | Â |
8 | Â | Â | Â | Â | Â | Â | Â |
9 | Â | Â | Â | Â | Â | 21q | deletion |
1q,6p,8q,9q,20q,22q | amplification |