Table 1 Gene mutations detected with NGS

BTG2

SNV

64.96

|c.19A>G

|p.Thr7Ala

|missense

NR_034151.1|NM_006763.2

chr1:203274753

ITPKB

SNV

70.99

c.964G>A

p.Ala322Thr

missense

NM_002221.3

chr1:226924196

TET2

SNV

42.44

c.3116C>T|

p.Ser1039Leu|

missense|

NM_001127208.2|NR_126420.1

chr4:106158215

FAT1

SNV

27.94

c.9514T>C

p.Phe3172Leu

missense

NM_005245.3

chr4:187532879

FAT1

SNV

25.8

c.6156A>C

p.Glu2052Asp

missense

NM_005245.3

chr4:187541584

PIM1

SNV

35.92

c.202C>T

p.His68Tyr

missense

NM_002648.3

chr6:37138769

CARD11

SNV

27.78

c.1010G>A

p.Arg337Gln

missense

NM_032415.5

chr7:2978320

CARD11

SNV

26.91

c.739A>G

p.Arg247Gly

missense

NM_032415.5

chr7:2979508

KMT2C

SNV

54.56

c.2512G>A

p.Gly838Ser

missense

NM_170606.2

chr7:151945007

NOTCH1

SNV

32.78

c.5476G>A

p.Glu1826Lys

missense

NM_017617.4

chr9:139396362

KMT2D

SNV

61.97

c.10045A>G

p.Met3349Val

missense

NM_003482.3

chr12:49431094

SOCS1

SNV

33.75

c.7G>C

p.Ala3Pro

missense

NM_003745.1

chr16:11349329

BCORL1

SNV

98.43

c.331T>C

p.Phe111Leu

missense

NM_021946.4

chrX:129147079