Details of all the somatic mutations in the study
UPN . | Gene . | Mutant allele burden (%) . | Variant class . | Nucleotide and protein change . | Constitutional DNA . |
---|---|---|---|---|---|
2* | ASXL1 | 30 | Frameshift insertion | c.1927_1928insG:p.G643fs | Skin |
2* | DNMT3A | 42 | Nonsynonymous SNV | c.C1540G:p.L514V | Skin |
2* | ERBB2 | 44 | Nonsynonymous SNV | c.G922A:p.V308M | Skin |
5* | TET2 | 5 | Stopgain SNV | c.C3100T:p.Q1034X | Skin |
6* | ASXL1 | 38 | Stopgain SNV | c.C2242T:p.Q748X | Buccal |
10* | SRSF2 | 43 | Nonsynonymous SNV | c.C284T:p.P95L | Buccal |
16* | ASXL1 | 23 | Frameshift insertion | c.2469_2470insAG:p.L823fs | Skin |
18* | DNMT3A | 31 | Nonsynonymous SNV | c.C2644T:p.R882C | Skin |
19* | IKZF1 | 14 | Nonsynonymous SNV | c.C640G:p.H214D | Skin |
21* | BCOR | 5 | Stopgain SNV | c.C526T:p.Q176X | Buccal |
29* | ASXL1 | 41 | Stopgain SNV | c.G4068A:p.W1356X | Skin |
33* | BCOR | 68 | Stopgain SNV | c.G4832A:p.W1611X | Skin |
40* | ASXL1 | 31 | Nonframeshift deletion | c.2894_2896del:p.965_966del | Buccal |
46* | MPL | 10 | Nonsynonymous SNV | c.G1544T:p.W515L | Buccal |
64 | DNMT3A | 47 | Nonsynonymous SNV | c.C2644T:p.R882C | Skin |
66 | ASXL1 | 37 | Frameshift deletion | c.2433delT:p.N811fs | Skin |
67 | U2AF1 | 19 | Nonsynonymous SNV | c.C101A:p.S34Y | Skin |
69 | ASXL1 | 34 | Stopgain SNV | c.C2077T:p.R693X | Buccal |
70 | ASXL1 | 2 | Stopgain SNV | c.G2026T:p.E676X | Buccal |
70 | BCOR | 14 | Stopgain SNV | c.T912G:p.Y304X | Buccal |
73 | BCOR | 6 | Frameshift insertion | c.4834_4835insC:p.L1612fs | Skin |
79 | ASXL1 | 36 | Stopgain SNV | c.G2026T:p.E676X | Buccal |
81 | ASXL1 | 3 | Stopgain SNV | c.T2324G:p.L775X | Skin |
88 | ASXL1 | 7 | Frameshift deletion | c.2126delC:p.A709fs | Skin |
93 | DNMT3A | 8 | Stopgain SNV | C2311T:p.R771X | Skin |
94 | BCOR | 30 | Splice site | splice site c.3052-2A>G | Skin |
97 | DNMT3A | 7 | Nonsynonymous SNV | c.C2644T:p.R882C | Buccal |
107 | ASXL1 | 30 | Stopgain SNV | c.T2468G:p.L823X | Buccal |
129 | DNMT3A | 5 | Nonsynonymous SNV | c.G2207A:p.R736H | Skin |
130 | DNMT3A | 5 | Nonsynonymous SNV | c.G2645A:p.R882H | Skin |
140 | BCOR | 5 | Frameshift deletion | c.4760delC:p.P1587fs | Buccal |
142 | DNMT3A | 1.5 | Nonsynonymous SNV | c.C2644T:p.R882C | Buccal |
UPN . | Gene . | Mutant allele burden (%) . | Variant class . | Nucleotide and protein change . | Constitutional DNA . |
---|---|---|---|---|---|
2* | ASXL1 | 30 | Frameshift insertion | c.1927_1928insG:p.G643fs | Skin |
2* | DNMT3A | 42 | Nonsynonymous SNV | c.C1540G:p.L514V | Skin |
2* | ERBB2 | 44 | Nonsynonymous SNV | c.G922A:p.V308M | Skin |
5* | TET2 | 5 | Stopgain SNV | c.C3100T:p.Q1034X | Skin |
6* | ASXL1 | 38 | Stopgain SNV | c.C2242T:p.Q748X | Buccal |
10* | SRSF2 | 43 | Nonsynonymous SNV | c.C284T:p.P95L | Buccal |
16* | ASXL1 | 23 | Frameshift insertion | c.2469_2470insAG:p.L823fs | Skin |
18* | DNMT3A | 31 | Nonsynonymous SNV | c.C2644T:p.R882C | Skin |
19* | IKZF1 | 14 | Nonsynonymous SNV | c.C640G:p.H214D | Skin |
21* | BCOR | 5 | Stopgain SNV | c.C526T:p.Q176X | Buccal |
29* | ASXL1 | 41 | Stopgain SNV | c.G4068A:p.W1356X | Skin |
33* | BCOR | 68 | Stopgain SNV | c.G4832A:p.W1611X | Skin |
40* | ASXL1 | 31 | Nonframeshift deletion | c.2894_2896del:p.965_966del | Buccal |
46* | MPL | 10 | Nonsynonymous SNV | c.G1544T:p.W515L | Buccal |
64 | DNMT3A | 47 | Nonsynonymous SNV | c.C2644T:p.R882C | Skin |
66 | ASXL1 | 37 | Frameshift deletion | c.2433delT:p.N811fs | Skin |
67 | U2AF1 | 19 | Nonsynonymous SNV | c.C101A:p.S34Y | Skin |
69 | ASXL1 | 34 | Stopgain SNV | c.C2077T:p.R693X | Buccal |
70 | ASXL1 | 2 | Stopgain SNV | c.G2026T:p.E676X | Buccal |
70 | BCOR | 14 | Stopgain SNV | c.T912G:p.Y304X | Buccal |
73 | BCOR | 6 | Frameshift insertion | c.4834_4835insC:p.L1612fs | Skin |
79 | ASXL1 | 36 | Stopgain SNV | c.G2026T:p.E676X | Buccal |
81 | ASXL1 | 3 | Stopgain SNV | c.T2324G:p.L775X | Skin |
88 | ASXL1 | 7 | Frameshift deletion | c.2126delC:p.A709fs | Skin |
93 | DNMT3A | 8 | Stopgain SNV | C2311T:p.R771X | Skin |
94 | BCOR | 30 | Splice site | splice site c.3052-2A>G | Skin |
97 | DNMT3A | 7 | Nonsynonymous SNV | c.C2644T:p.R882C | Buccal |
107 | ASXL1 | 30 | Stopgain SNV | c.T2468G:p.L823X | Buccal |
129 | DNMT3A | 5 | Nonsynonymous SNV | c.G2207A:p.R736H | Skin |
130 | DNMT3A | 5 | Nonsynonymous SNV | c.G2645A:p.R882H | Skin |
140 | BCOR | 5 | Frameshift deletion | c.4760delC:p.P1587fs | Buccal |
142 | DNMT3A | 1.5 | Nonsynonymous SNV | c.C2644T:p.R882C | Buccal |
c, nucleotide; g, genomic sequence; p, protein sequence; SNV, single nucleotide variant.
Indicates patients in the initial cohort (UPN 1 through UPN 57); the correlation with PIGA mutation is illustrated in supplemental Table 4.