Diagnoses, cytogenetics, and mutations in patients with GATA2 deficiency
Pt . | Family pedigree . | GATA2 mutation . | Disease . | Cytogenetics . | Sex . | Inheritance . | BMT . | Survival . | Common mutations . | Total filtered variants . |
---|---|---|---|---|---|---|---|---|---|---|
1 | 35.III.3 | c.1061C>T; p.T354M | MDS | Trisomy 8 | M | Familial | Yes | Deceased | 0 | 1 |
2 | 25.II.1 | c.1017 + 572C>T | G2BMID | Normal | M | Familial | No | Deceased | ASXL1, PTPN11, SMC1A, STAG2 | 5 |
3 | 8.I.1 | c.243_244delAinsGC; p.G82fs | G2BMID | Normal | M | De novo | Yes | Alive | DNMT3A, STAG2 | 4 |
4 | 12.I.1 | c.1084_1095del12; p.R362del4 | MDS | Monosomy 7, trisomy 21 | M | Unknown | Yes | Deceased | 0 | 10 |
5 | 17.I.1 | c.1061C>T; p.T354M | MDS | Trisomy 8 | M | Familial | Yes | Alive | 0 | 3 |
6 | 17.II.1 | c.1061C>T; p.T354M | G2BMID | Normal | M | Familial | Yes | Alive | STAG2 | 5 |
7 | 26.I.1 | c.302delG; p.G101fs | CMML | del(11)(q13q23) | F | Unknown | Yes | Deceased | ASXL1, CBL, DNMT3A | 13 |
8 | 34.II.2 | c.1116_1130del15; p.C373del5 | MDS | Monosomy 7 | M | Familial | Yes | Deceased | STAG2 | 5 |
9 | 34.I.1 | c.1116_1130del15; p.C373del5 | G2BMID | Normal | F | Familial | No | Alive | 0 | 5 |
10 | 31.II.2 | c.1187G>A; p.R396Q | G2BMID | Normal | M | Familial | Yes | Alive | STAG2 | 4 |
11 | 27.I.1 | c.586_593dup; p.G199fs | MDS | del(9)(q13q22) | F | Familial | Yes | Alive | ASXL1 | 6 |
12 | 39.I.2 | c.988C>T; p.R330X | MDS | Trisomy 8 | F | Familial | Yes | Alive | 0 | 4 |
13 | 39.I.1 | c.988C>T; p.R330X | MDS | Trisomy 8 | F | Familial | Yes | Alive | STAG2 | 2 |
14 | 15.I.1 | c.1186C>T; p.R396W | G2BMID | Normal | F | De novo | Yes | Alive | STAG2 | 4 |
15 | 38.I.1 | c.417dupT; p.V140Cfs | G2BMID | Normal | F | De novo | Yes | Alive | ASXL1, JAK2 | 12 |
16 | 9.II.1 | c.1192C>T; p.R398W | MDS | Normal | M | Familial | No | Deceased | BCOR, SRSF2, STAG* | 12 |
17 | 9.III.2 | c.1192C>T; p.R398W | Asymptomatic | Normal | M | Familial | No | Alive | 0 | 4 |
18 | 41.I.1 | c.1009C>T; p.R337X | G2BMID | Normal | F | De novo | Yes | Alive | ASXL1, DNMT3A, SMC1A | 14 |
19 | 42.I.1 | c.1186C>T; p.R396W | G2BMID | Normal | M | Familial | Yes | Alive | KDM2A | 2 |
20 | 14.I.1 | c.1187G>A; p.R396Q | G2BMID | Normal | F | De novo | No | Deceased | ASXL1, STAG2 | 9 |
21 | 146.I.1 | c.1082G>A; p.R361H | MDS | Normal | M | Familial | No | Deceased | DNMT3A, STAG2 | 7 |
22 | 159.I.1 | Unknown | AML | Trisomy 8, Monosomy 13 | F | Unknown | Yes | Deceased | KMT2A, MECOM | 14 |
23 | 48.II.11 | c.1017 + 572C>T | Asymptomatic | Normal | F | Familial | No | Alive | CUX1, DNMT3A, KMT2A,* U2 AF1 | 7 |
24 | 126.III.4† | Unknown | MDS | Trisomy 8 | F | Familial | Yes | Alive | 0 | 1 |
25 | 48.III.14 | c.1017 + 572C>T | G2BMID | der(1;14)(q10;p10), trisomy 21 | F | Familial | Yes | Alive | STAG2 | 1 |
26 | 126.III.23† | Unknown | MDS | Trisomy 8 | M | Familial | Yes | Alive | STAG2* | 3 |
27 | 126.II.8† | Unknown | Asymptomatic | Normal | F | Familial | No | Alive | 0 | 1 |
28 | 126.II.4† | Unknown | Asymptomatic | Normal | M | Familial | No | Alive | 0 | 0 |
29 | 256.I.1 | c.1123C>T; p.L375S | AML | Trisomy 8, trisomy 20 | F | De novo | Yes | Deceased | NRAS | 5 |
30 | 218.I.1 | c.1114G>A; p.A372T | MDS | Trisomy 8 | F | Fe novo | No | Deceased | DNMT3A | 10 |
31 | 129.I.1 | c.802G>T; p.G268X | MDS | del(13)(q12q14) | F | Unknown | No | Alive | 0 | 2 |
32 | 233.I.1 | c.803delG; p.G268fs | G2BMID | Normal | F | De novo | Yes | Alive | 0 | 11 |
33 | 203.I.1 | c.1021delG; p.A341Pfs | G2BMID | Normal | M | Familial | Yes | Alive | DNMT3A | 6 |
34 | 47.I.1 | c.1084C>T; p.R362X | Asymptomatic | Normal | F | Familial | No | Alive | 0 | 1 |
35 | 270.I.1 | c.1082G>A; p.R361H | G2BMID | Normal | M | Familial | Yes | Alive | BCOR | 7 |
36 | 49.III.2 | c.1084C>T; p.R362X | G2BMID | Normal | F | Familial | Yes | Alive | 0 | 3 |
37 | 281.I.1 | c.1186C>T; p.R396W | MDS | inv(9)(p12q13) | F | Unknown | Yes | Deceased | ASXL1 | 5 |
38 | 50.II.2 | c.1128C>A; p.Y376X | MDS | Normal | F | Familial | Yes | Alive | STAG2 | 3 |
39 | 50.II.1 | c.1128C>A; p.Y376X | MDS | der(1;7)(q10;p10), trisomy 8 | M | Familial | Yes | Alive | STAG2 | 14 |
40 | 293.I.1 | Unknown | AML | der(5) t(5;13)(q13q13) | M | Unknown | Yes | Alive | 0 | 5 |
41 | 291.I.1 | c.1084C>T; p.R362X | MDS | Monosomy 7 | M | De novo | Yes | Alive | STAG2 | 2 |
42 | 216.I.1 | c.1192C>T; p.R398W | MDS | der(1;7)(q10;p10), 1+der(1;13)(q10;q10), trisomy 8, monosomy X | F | Unknown | Yes | Alive | ASXL1 | 7 |
43 | 51.III.1 | c.1192C>T; p.R398W | G2BMID | Normal | F | Familial | Yes | Deceased | ASXL1 | 6 |
44 | 51.II.1 | c.1192C>T; p.R398W | Asymptomatic | Normal | M | Familial | No | Alive | 0 | 2 |
45 | 52.II.4 | c.1082G>C; p.R361P | G2BMID | Normal | F | Familial | No | Alive | BCL9 | 2 |
46 | 52.II.5 | c.1082G>C; p.R361P | G2BMID | Normal | F | Familial | No | Alive | 0 | 4 |
47 | 52.I.4 | c.1082G>C; p.R361P | MDS | Normal | M | Familial | Yes | Deceased | STAG2 | 4 |
48 | 330.I.1 | c.898dupG; p.A300Gfs | MDS | Normal | F | Familial | Yes | Deceased | ASXL1, BCOR | 5 |
49 | 335.III.1 | c.1017 + 572C>T | MDS | Normal | F | Familial | Yes | Alive | 0 | 1 |
50 | 340.II.1 | c.1159_1160dupAC; p.M388fs | G2BMID | Monosomy 7, der(1;7)(q10;p10), del(13)(q12q22) | M | Familial | Yes | Alive | STAG2‡ | 3 |
51 | 324.I.1 | c.1018del7; p.S340fs | MDS | Trisomy 8 | F | De novo | Yes | Alive | STAG2 | 6 |
52 | 342.I.1 | c.1017 + 572C>T | MDS | Monosomy 7 | M | Unknown | Yes | Alive | SAMD9, SETBP1, U2AF1 | 7 |
53 | 53.V.4 | c.1017 + 572C>T | G2BMID | Normal | F | Familial | No | Alive | 0 | 2 |
54 | 53.V.3 | c.1017 + 572C>T | MDS | Normal | F | Familial | Yes | Alive | ETV6 | 3 |
55 | 350.I.1 | c.248delA; p.Q83Rfs‡ | MDS | Normal | F | De novo | Yes | Alive | 0 | 4 |
56 | 349.II.4 | c.1192C>T; p.R398W | MDS | trp(1)(q21q32) | F | Familial | No | Alive | DNMT3A,* U2 AF1 | 11 |
57 | 347.I.1 | c.1017 + 2T>A | MDS | Normal | F | De novo | Yes | Alive | STAG2 | 5 |
58 | 351.I.1 | c.1192C>T; p.R398W | MDS | Normal | F | De novo | Yes | Alive | 0 | 2 |
59 | 333.II.3 | c.1018-50_1143 + 247del; p.S340-N381del | MDS | Trisomy 8 | M | Familial | Yes | Alive | DNMT3A, STAG2* | 6 |
60 | 337.I.1 | c.921dupG; p.R308Afs‡ | G2BMID | Normal | F | Unknown | Yes | Alive | STAG2 | 12 |
61 | 360.I.1 | c.1024_1025insGCCG; p.A342Gfs | G2BMID | Normal | F | Unknown | Yes | Alive | STAG2 | 2 |
62 | 357.II.1 | c.1017 + 1G>T‡ | MDS | Monosomy 7 | F | Familial | Yes | Alive | RUNX1 | 4 |
63 | 357.I.1 | c.1017 + 1G>T‡ | MDS | Trisomy 8 | F | Familial | No | Alive | ASXL1 | 6 |
64 | 362.I.1 | c.247C>T; p.Q83X‡ | MDS | Monosomy 7 | F | De novo | Yes | Alive | STAG2* | 5 |
65 | n/a | c.1084C>T; p.R362X | G2BMID | Normal | F | De novo | No | Deceased | NOTCH2 | 6 |
66 | n/a | c.680_683del; p.S227fs‡ | G2BMID | Normal | F | De novo | Yes | Alive | STAG2 | 4 |
67 | 365.I.1 | c.1081C>T; p.R361C | MDS | der(1;7)(q10;p10), trisomy 8 | M | Familial | Yes | Alive | STAG2* | 7 |
68 | 368.I.1 | c.1061C>T; p.T354M | Asymptomatic | Unknown | F | Familial | No | Alive | DNMT3A | 7 |
69 | 370.I.1 | unknown | MDS | Normal | F | Unknown | Yes | Deceased | ASXL1, RUNX1 | 10 |
70 | 375.I.2 | c.1192C>T; p.R398W | MDS | (1)t(1;15), Trisomy 8 | F | Familial | Yes | Alive | ASXL1, CUX1, RAD21 | 10 |
71 | n/a | c.1150delA; p.R384fs‡ | G2BMID | Normal | M | De novo | Yes | Alive | 0 | 2 |
72 | 378.I.1 | c.1021delG; p.A341Pfs | MDS | Normal | M | unknown | Yes | Alive | BCOR | 5 |
73 | 379.I.1 | c.1277C>G; p.S426C‡ | G2BMID | Normal | F | Unknown | No | Alive | 0 | 3 |
74 | 367.I.1 | unknown | MDS | Trisomy 8 | F | Unknown | Yes | Alive | 0 | 2 |
75 | 382.I.2 | c.1061C>A; p.T354K | MDS | Normal | F | Familial | Yes | Alive | 0 | 7 |
76 | 283.II.1 | c.58C>T; p.Q20X‡ | MDS | der(1;7)(q10:p10) | F | Familial | Yes | Alive | SETBP1, STAG2 | 5 |
77 | n/a | c.1061C>T; p.T354M | G2BMID | Normal | F | De novo | Yes | Alive | 0 | 3 |
78 | 4.III.5 | c.1017 + 572C>T | CMML | Monosomy 7 | M | familial | Yes | Alive | ASXL1, SETBP1, U2AF1 | 26 |
79 | 384.I.1 | c.1192C>T; p.R398W | MDS | Monosomy 7 | F | Familial | Yes | Alive | ASXL1 | 4 |
80 | n/a | c.1192C>T; p.R398W | G2BMID | Normal | F | Familial | No | Alive | 0 | 2 |
81 | 393.II.1 | c.1061C>T; p.T354M | G2BMID | Normal | F | Familial | No | Alive | 0 | 9 |
82 | n/a | c.840delT; p.K281Sfs‡ | G2BMID | Normal | F | De novo | Yes | Alive | 0 | 3 |
83 | 390.I.1 | c.1009C>T; p.R337X | G2BMID | Normal | F | De novo | Yes | Alive | ASXL1, STAG2 | 4 |
84 | 394.I.1 | c.1114G>A; p.A372T | G2BMID | Normal | M | Unknown | Yes | Alive | 0 | 6 |
85 | 349.IV.5 | c.1192C>T; p.R398W | G2BMID | Normal | M | Familial | Yes | Alive | 0 | 1 |
86 | 349.III.16 | c.1192C>T; p.R398W | MDS | Trisomy 8 | F | Familial | Yes | Alive | 0 | 4 |
87 | 349.IV.7 | c.1192C>T; p.R398W | G2BMID | Normal | F | Familial | No | Alive | 0 | 4 |
88 | 1.IV.1 | c.1192C>T; p.R398W | G2BMID | Normal | F | Familial | Yes | Alive | 0 | 3 |
89 | 1.III.2 | c.1192C>T; p.R398W | Asymptomatic | Normal | M | Familial | No | Alive | DNMT3A | 5 |
90 | 389.I.1 | c.1024_1025insG; p.A342Gfs | G2BMID | Normal | F | Unknown | Yes | Alive | 0 | 8 |
91 | 4.III.2 | c.1017 + 572C>T | G2BMID | Normal | F | Familial | No | Alive | 0 | NA |
92 | 37.I.1 | c.1081C>T, p.R361C | MDS | Normal | F | De novo | Yes | Alive | DNMT3A, FLT3 | NA |
93 | 48.II.6 | c.1017 + 572C>T | Asymptomatic | Normal | F | Familial | No | Alive | 0 | NA |
94 | 48.II.2 | c.1017 + 572C>T | Asymptomatic | Normal | F | Familial | No | Alive | 0 | NA |
95 | n/a | c.1187G>A; p.R396Q | MDS | Normal | F | Familial | Yes | Alive | ASXL1 | NA |
96 | 4.III.1 | c.1017 + 572C>T | Asymptomatic | Normal | M | Familial | No | Alive | 0 | NA |
97 | 4.I.1 | c.1017 + 572C>T | CMML | Normal | M | Familial | No | Alive | 0 | NA |
98 | 17.II.2 | c.1061C>T; p.T354M | G2BMID | Normal | M | Familial | No | Alive | 0 | NA |
99 | 48.II.8 | c.1017 + 572C>T | Asymptomatic | Normal | M | Familial | No | Alive | 0 | NA |
100 | 4.III.4 | c.1017 + 572C>T | MDS | Monosomy 7, Trisomy 8 | M | Familial | Yes | Alive | 0 | NA |
101 | n/a | c.839delC; p.P280Lfs | MDS | Trisomy 8 | M | Unknown | No | Alive | 0 | NA |
102 | 6.I.1 | c.1017 + 512del28 | Asymptomatic | Normal | M | Familial | No | Alive | 0 | NA |
103 | 335.II.1 | c.1017 + 572C>T | Asymptomatic | Normal | F | Familial | No | Alive | 0 | NA |
104 | n/a | c.1084C>T; p.R362X | G2BMID | Normal | M | De novo | No | Alive | STAG2* | 5 |
105 | 277.I.1 | c.1187G>A; p.R396Q | MDS | Trisomy 8 | F | De novo | Yes | Alive | 0 | 4 |
106 | 368.II.1 | c.1061C>T; p.T354M | MDS | Monosomy 7 | M | Familial | Yes | Alive | 0 | NA |
Pt . | Family pedigree . | GATA2 mutation . | Disease . | Cytogenetics . | Sex . | Inheritance . | BMT . | Survival . | Common mutations . | Total filtered variants . |
---|---|---|---|---|---|---|---|---|---|---|
1 | 35.III.3 | c.1061C>T; p.T354M | MDS | Trisomy 8 | M | Familial | Yes | Deceased | 0 | 1 |
2 | 25.II.1 | c.1017 + 572C>T | G2BMID | Normal | M | Familial | No | Deceased | ASXL1, PTPN11, SMC1A, STAG2 | 5 |
3 | 8.I.1 | c.243_244delAinsGC; p.G82fs | G2BMID | Normal | M | De novo | Yes | Alive | DNMT3A, STAG2 | 4 |
4 | 12.I.1 | c.1084_1095del12; p.R362del4 | MDS | Monosomy 7, trisomy 21 | M | Unknown | Yes | Deceased | 0 | 10 |
5 | 17.I.1 | c.1061C>T; p.T354M | MDS | Trisomy 8 | M | Familial | Yes | Alive | 0 | 3 |
6 | 17.II.1 | c.1061C>T; p.T354M | G2BMID | Normal | M | Familial | Yes | Alive | STAG2 | 5 |
7 | 26.I.1 | c.302delG; p.G101fs | CMML | del(11)(q13q23) | F | Unknown | Yes | Deceased | ASXL1, CBL, DNMT3A | 13 |
8 | 34.II.2 | c.1116_1130del15; p.C373del5 | MDS | Monosomy 7 | M | Familial | Yes | Deceased | STAG2 | 5 |
9 | 34.I.1 | c.1116_1130del15; p.C373del5 | G2BMID | Normal | F | Familial | No | Alive | 0 | 5 |
10 | 31.II.2 | c.1187G>A; p.R396Q | G2BMID | Normal | M | Familial | Yes | Alive | STAG2 | 4 |
11 | 27.I.1 | c.586_593dup; p.G199fs | MDS | del(9)(q13q22) | F | Familial | Yes | Alive | ASXL1 | 6 |
12 | 39.I.2 | c.988C>T; p.R330X | MDS | Trisomy 8 | F | Familial | Yes | Alive | 0 | 4 |
13 | 39.I.1 | c.988C>T; p.R330X | MDS | Trisomy 8 | F | Familial | Yes | Alive | STAG2 | 2 |
14 | 15.I.1 | c.1186C>T; p.R396W | G2BMID | Normal | F | De novo | Yes | Alive | STAG2 | 4 |
15 | 38.I.1 | c.417dupT; p.V140Cfs | G2BMID | Normal | F | De novo | Yes | Alive | ASXL1, JAK2 | 12 |
16 | 9.II.1 | c.1192C>T; p.R398W | MDS | Normal | M | Familial | No | Deceased | BCOR, SRSF2, STAG* | 12 |
17 | 9.III.2 | c.1192C>T; p.R398W | Asymptomatic | Normal | M | Familial | No | Alive | 0 | 4 |
18 | 41.I.1 | c.1009C>T; p.R337X | G2BMID | Normal | F | De novo | Yes | Alive | ASXL1, DNMT3A, SMC1A | 14 |
19 | 42.I.1 | c.1186C>T; p.R396W | G2BMID | Normal | M | Familial | Yes | Alive | KDM2A | 2 |
20 | 14.I.1 | c.1187G>A; p.R396Q | G2BMID | Normal | F | De novo | No | Deceased | ASXL1, STAG2 | 9 |
21 | 146.I.1 | c.1082G>A; p.R361H | MDS | Normal | M | Familial | No | Deceased | DNMT3A, STAG2 | 7 |
22 | 159.I.1 | Unknown | AML | Trisomy 8, Monosomy 13 | F | Unknown | Yes | Deceased | KMT2A, MECOM | 14 |
23 | 48.II.11 | c.1017 + 572C>T | Asymptomatic | Normal | F | Familial | No | Alive | CUX1, DNMT3A, KMT2A,* U2 AF1 | 7 |
24 | 126.III.4† | Unknown | MDS | Trisomy 8 | F | Familial | Yes | Alive | 0 | 1 |
25 | 48.III.14 | c.1017 + 572C>T | G2BMID | der(1;14)(q10;p10), trisomy 21 | F | Familial | Yes | Alive | STAG2 | 1 |
26 | 126.III.23† | Unknown | MDS | Trisomy 8 | M | Familial | Yes | Alive | STAG2* | 3 |
27 | 126.II.8† | Unknown | Asymptomatic | Normal | F | Familial | No | Alive | 0 | 1 |
28 | 126.II.4† | Unknown | Asymptomatic | Normal | M | Familial | No | Alive | 0 | 0 |
29 | 256.I.1 | c.1123C>T; p.L375S | AML | Trisomy 8, trisomy 20 | F | De novo | Yes | Deceased | NRAS | 5 |
30 | 218.I.1 | c.1114G>A; p.A372T | MDS | Trisomy 8 | F | Fe novo | No | Deceased | DNMT3A | 10 |
31 | 129.I.1 | c.802G>T; p.G268X | MDS | del(13)(q12q14) | F | Unknown | No | Alive | 0 | 2 |
32 | 233.I.1 | c.803delG; p.G268fs | G2BMID | Normal | F | De novo | Yes | Alive | 0 | 11 |
33 | 203.I.1 | c.1021delG; p.A341Pfs | G2BMID | Normal | M | Familial | Yes | Alive | DNMT3A | 6 |
34 | 47.I.1 | c.1084C>T; p.R362X | Asymptomatic | Normal | F | Familial | No | Alive | 0 | 1 |
35 | 270.I.1 | c.1082G>A; p.R361H | G2BMID | Normal | M | Familial | Yes | Alive | BCOR | 7 |
36 | 49.III.2 | c.1084C>T; p.R362X | G2BMID | Normal | F | Familial | Yes | Alive | 0 | 3 |
37 | 281.I.1 | c.1186C>T; p.R396W | MDS | inv(9)(p12q13) | F | Unknown | Yes | Deceased | ASXL1 | 5 |
38 | 50.II.2 | c.1128C>A; p.Y376X | MDS | Normal | F | Familial | Yes | Alive | STAG2 | 3 |
39 | 50.II.1 | c.1128C>A; p.Y376X | MDS | der(1;7)(q10;p10), trisomy 8 | M | Familial | Yes | Alive | STAG2 | 14 |
40 | 293.I.1 | Unknown | AML | der(5) t(5;13)(q13q13) | M | Unknown | Yes | Alive | 0 | 5 |
41 | 291.I.1 | c.1084C>T; p.R362X | MDS | Monosomy 7 | M | De novo | Yes | Alive | STAG2 | 2 |
42 | 216.I.1 | c.1192C>T; p.R398W | MDS | der(1;7)(q10;p10), 1+der(1;13)(q10;q10), trisomy 8, monosomy X | F | Unknown | Yes | Alive | ASXL1 | 7 |
43 | 51.III.1 | c.1192C>T; p.R398W | G2BMID | Normal | F | Familial | Yes | Deceased | ASXL1 | 6 |
44 | 51.II.1 | c.1192C>T; p.R398W | Asymptomatic | Normal | M | Familial | No | Alive | 0 | 2 |
45 | 52.II.4 | c.1082G>C; p.R361P | G2BMID | Normal | F | Familial | No | Alive | BCL9 | 2 |
46 | 52.II.5 | c.1082G>C; p.R361P | G2BMID | Normal | F | Familial | No | Alive | 0 | 4 |
47 | 52.I.4 | c.1082G>C; p.R361P | MDS | Normal | M | Familial | Yes | Deceased | STAG2 | 4 |
48 | 330.I.1 | c.898dupG; p.A300Gfs | MDS | Normal | F | Familial | Yes | Deceased | ASXL1, BCOR | 5 |
49 | 335.III.1 | c.1017 + 572C>T | MDS | Normal | F | Familial | Yes | Alive | 0 | 1 |
50 | 340.II.1 | c.1159_1160dupAC; p.M388fs | G2BMID | Monosomy 7, der(1;7)(q10;p10), del(13)(q12q22) | M | Familial | Yes | Alive | STAG2‡ | 3 |
51 | 324.I.1 | c.1018del7; p.S340fs | MDS | Trisomy 8 | F | De novo | Yes | Alive | STAG2 | 6 |
52 | 342.I.1 | c.1017 + 572C>T | MDS | Monosomy 7 | M | Unknown | Yes | Alive | SAMD9, SETBP1, U2AF1 | 7 |
53 | 53.V.4 | c.1017 + 572C>T | G2BMID | Normal | F | Familial | No | Alive | 0 | 2 |
54 | 53.V.3 | c.1017 + 572C>T | MDS | Normal | F | Familial | Yes | Alive | ETV6 | 3 |
55 | 350.I.1 | c.248delA; p.Q83Rfs‡ | MDS | Normal | F | De novo | Yes | Alive | 0 | 4 |
56 | 349.II.4 | c.1192C>T; p.R398W | MDS | trp(1)(q21q32) | F | Familial | No | Alive | DNMT3A,* U2 AF1 | 11 |
57 | 347.I.1 | c.1017 + 2T>A | MDS | Normal | F | De novo | Yes | Alive | STAG2 | 5 |
58 | 351.I.1 | c.1192C>T; p.R398W | MDS | Normal | F | De novo | Yes | Alive | 0 | 2 |
59 | 333.II.3 | c.1018-50_1143 + 247del; p.S340-N381del | MDS | Trisomy 8 | M | Familial | Yes | Alive | DNMT3A, STAG2* | 6 |
60 | 337.I.1 | c.921dupG; p.R308Afs‡ | G2BMID | Normal | F | Unknown | Yes | Alive | STAG2 | 12 |
61 | 360.I.1 | c.1024_1025insGCCG; p.A342Gfs | G2BMID | Normal | F | Unknown | Yes | Alive | STAG2 | 2 |
62 | 357.II.1 | c.1017 + 1G>T‡ | MDS | Monosomy 7 | F | Familial | Yes | Alive | RUNX1 | 4 |
63 | 357.I.1 | c.1017 + 1G>T‡ | MDS | Trisomy 8 | F | Familial | No | Alive | ASXL1 | 6 |
64 | 362.I.1 | c.247C>T; p.Q83X‡ | MDS | Monosomy 7 | F | De novo | Yes | Alive | STAG2* | 5 |
65 | n/a | c.1084C>T; p.R362X | G2BMID | Normal | F | De novo | No | Deceased | NOTCH2 | 6 |
66 | n/a | c.680_683del; p.S227fs‡ | G2BMID | Normal | F | De novo | Yes | Alive | STAG2 | 4 |
67 | 365.I.1 | c.1081C>T; p.R361C | MDS | der(1;7)(q10;p10), trisomy 8 | M | Familial | Yes | Alive | STAG2* | 7 |
68 | 368.I.1 | c.1061C>T; p.T354M | Asymptomatic | Unknown | F | Familial | No | Alive | DNMT3A | 7 |
69 | 370.I.1 | unknown | MDS | Normal | F | Unknown | Yes | Deceased | ASXL1, RUNX1 | 10 |
70 | 375.I.2 | c.1192C>T; p.R398W | MDS | (1)t(1;15), Trisomy 8 | F | Familial | Yes | Alive | ASXL1, CUX1, RAD21 | 10 |
71 | n/a | c.1150delA; p.R384fs‡ | G2BMID | Normal | M | De novo | Yes | Alive | 0 | 2 |
72 | 378.I.1 | c.1021delG; p.A341Pfs | MDS | Normal | M | unknown | Yes | Alive | BCOR | 5 |
73 | 379.I.1 | c.1277C>G; p.S426C‡ | G2BMID | Normal | F | Unknown | No | Alive | 0 | 3 |
74 | 367.I.1 | unknown | MDS | Trisomy 8 | F | Unknown | Yes | Alive | 0 | 2 |
75 | 382.I.2 | c.1061C>A; p.T354K | MDS | Normal | F | Familial | Yes | Alive | 0 | 7 |
76 | 283.II.1 | c.58C>T; p.Q20X‡ | MDS | der(1;7)(q10:p10) | F | Familial | Yes | Alive | SETBP1, STAG2 | 5 |
77 | n/a | c.1061C>T; p.T354M | G2BMID | Normal | F | De novo | Yes | Alive | 0 | 3 |
78 | 4.III.5 | c.1017 + 572C>T | CMML | Monosomy 7 | M | familial | Yes | Alive | ASXL1, SETBP1, U2AF1 | 26 |
79 | 384.I.1 | c.1192C>T; p.R398W | MDS | Monosomy 7 | F | Familial | Yes | Alive | ASXL1 | 4 |
80 | n/a | c.1192C>T; p.R398W | G2BMID | Normal | F | Familial | No | Alive | 0 | 2 |
81 | 393.II.1 | c.1061C>T; p.T354M | G2BMID | Normal | F | Familial | No | Alive | 0 | 9 |
82 | n/a | c.840delT; p.K281Sfs‡ | G2BMID | Normal | F | De novo | Yes | Alive | 0 | 3 |
83 | 390.I.1 | c.1009C>T; p.R337X | G2BMID | Normal | F | De novo | Yes | Alive | ASXL1, STAG2 | 4 |
84 | 394.I.1 | c.1114G>A; p.A372T | G2BMID | Normal | M | Unknown | Yes | Alive | 0 | 6 |
85 | 349.IV.5 | c.1192C>T; p.R398W | G2BMID | Normal | M | Familial | Yes | Alive | 0 | 1 |
86 | 349.III.16 | c.1192C>T; p.R398W | MDS | Trisomy 8 | F | Familial | Yes | Alive | 0 | 4 |
87 | 349.IV.7 | c.1192C>T; p.R398W | G2BMID | Normal | F | Familial | No | Alive | 0 | 4 |
88 | 1.IV.1 | c.1192C>T; p.R398W | G2BMID | Normal | F | Familial | Yes | Alive | 0 | 3 |
89 | 1.III.2 | c.1192C>T; p.R398W | Asymptomatic | Normal | M | Familial | No | Alive | DNMT3A | 5 |
90 | 389.I.1 | c.1024_1025insG; p.A342Gfs | G2BMID | Normal | F | Unknown | Yes | Alive | 0 | 8 |
91 | 4.III.2 | c.1017 + 572C>T | G2BMID | Normal | F | Familial | No | Alive | 0 | NA |
92 | 37.I.1 | c.1081C>T, p.R361C | MDS | Normal | F | De novo | Yes | Alive | DNMT3A, FLT3 | NA |
93 | 48.II.6 | c.1017 + 572C>T | Asymptomatic | Normal | F | Familial | No | Alive | 0 | NA |
94 | 48.II.2 | c.1017 + 572C>T | Asymptomatic | Normal | F | Familial | No | Alive | 0 | NA |
95 | n/a | c.1187G>A; p.R396Q | MDS | Normal | F | Familial | Yes | Alive | ASXL1 | NA |
96 | 4.III.1 | c.1017 + 572C>T | Asymptomatic | Normal | M | Familial | No | Alive | 0 | NA |
97 | 4.I.1 | c.1017 + 572C>T | CMML | Normal | M | Familial | No | Alive | 0 | NA |
98 | 17.II.2 | c.1061C>T; p.T354M | G2BMID | Normal | M | Familial | No | Alive | 0 | NA |
99 | 48.II.8 | c.1017 + 572C>T | Asymptomatic | Normal | M | Familial | No | Alive | 0 | NA |
100 | 4.III.4 | c.1017 + 572C>T | MDS | Monosomy 7, Trisomy 8 | M | Familial | Yes | Alive | 0 | NA |
101 | n/a | c.839delC; p.P280Lfs | MDS | Trisomy 8 | M | Unknown | No | Alive | 0 | NA |
102 | 6.I.1 | c.1017 + 512del28 | Asymptomatic | Normal | M | Familial | No | Alive | 0 | NA |
103 | 335.II.1 | c.1017 + 572C>T | Asymptomatic | Normal | F | Familial | No | Alive | 0 | NA |
104 | n/a | c.1084C>T; p.R362X | G2BMID | Normal | M | De novo | No | Alive | STAG2* | 5 |
105 | 277.I.1 | c.1187G>A; p.R396Q | MDS | Trisomy 8 | F | De novo | Yes | Alive | 0 | 4 |
106 | 368.II.1 | c.1061C>T; p.T354M | MDS | Monosomy 7 | M | Familial | Yes | Alive | 0 | NA |
Patient (Pt) number and Family pedigree designation are listed chronologically as the samples were collected. The survival time is from first sample collection until the end of the study. Common mutations are those found in ≥3 patients in this study or >5% in other studies of myeloid malignancies. Mutations in patient 78 have also been described in Molina et al.67 NA indicates that WES was not performed (supplemental Table 1).
BMT, bone marrow transplant.
Two different variants were found in the gene for the indicated patient.
The pedigree for family 126 is given in supplemental Figure 3.
GATA2 mutations unique to our study.