Identified genes | Patient ID | Number of tumors with nonsynonymous mutation (frequency) | Chromosome | Position | Complementary DNA | Protein |
---|---|---|---|---|---|---|
CARD11 | KT80 |  |  | 2,979,501 | c.746A > T | p.Q249L |
KT80 | 3 | 7 | 2,959,246 | c.2270G > T | p.G757V | |
KT721 |  |  | 2,979,984 | c.298G > A | p.E100K | |
FNBP1 | KT720 KT721 | 2 | 9 | 94,012,949 132,686,175 | c.1118A > T c.1279A > T | p.E373V p.R427* |
GNAQ | KT80, KT721 KT79 | 3 | 9 | 80,537,229 80,537,135 | c.169A > T c.263A > T | p.K57* p.Q88L |
HOXD13 | KT79, KT722 | 2 | 2 | 176,957,650 | c.32G > C | p.G11A |
IKZF1 | KT80 KT81 | 2 | 7 | 50,450,403 50,367,232 | c.326C > G c.41-2A > T | p.S109C p.? |
MAX | KT79, KT81 | 2 | 14 | 65,472,892 | c.*30delC | p.? |
MLLT10 | KT720 KT80, KT721 KT81 | 4 | 10 | 21,903,809 21,959,631 21,875,221 | c.559A > T c.1049A > T c.241-2A > T | p.N187Y p.Q350L p.? |
NTRK3 | KT80, KT721 KT79 | 3 | 15 | 88,799,202 88,727,498 | c.183 T > A c.281 T > A | p.D61E p.L94H |
SEPTIN6 | KT80, KT721 KT81 | 3 | X | 118,763,455 118,786,815 | c.1106A > T c.528 + 2 T > A | p.D369V p.? |
SEPTIN9 | KT79, KT720 | 2 | 17 | 75,471,875 | c.275A > T | p.E92V |
SH3GL1 | KT81 KT79 | 2 | 19 | 4,362,684 4,361,737 | c.634C > T c.823G > C | p.R212W p.G275R |
SLC34A2 | KT80, KT721 KT17 | 3 | 4 | 25,674,846 25,677,770 | c.1183G > A c.1469A > T | p.A395T p.H490L |
TAL1 | KT720 KT720, KT722 KT720 | 3 | 1 | 47,691,377 47,685,603 47,685,597 | c.184G > C c.785 T > G c.791C > G | p.G62R p.V262G p.A264G |
TRAF7 | KT79 KT722 | 2 | 16 | 2,222,207 2,221,345 | c.491A > T c.429C > T | p.D164V - |