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Table 1 MED12 mutations, HMGA2 aberrations, and biallelic FH inactivation in uterine smooth muscle tumors

From: Characterization of MED12, HMGA2, and FH alterations reveals molecular variability in uterine smooth muscle tumors

Smooth muscle tumor subtype

Total

MED12 mutation positive

HMGA2 overexpressing

FH deficient

N

%

P-value

95% CI

N

%

P-value

95% CI

N

%

P-value

95% CI

Conventional

65

37

56.9

  

16

24.6

  

0

0

  

Histopathological UL variant

94

17

18.1

5.2 × 10−7

2.76–13.14

13

13.8

0.10

0.83–5.01

8

8.5

0.02

0.00–0.81

 Mitotically active

25

9

36

0.10

0.83–6.93

1

4

0.03

1.07–341.56

0

0

  

 Leiomyoma with bizarre nuclei

18

3

16.7

3.0 × 10−3

1.61–38.18

0

0

0.02

1.24- ∞

6

33.3

4.9 × 10−5

0.00–0.19

 Cellular

25

4

16

7.3 × 10−4

1.98–30.31

8

32

0.60

0.23–2.23

1

4

0.28

0.00–15.00

 Highly cellular

37

3

8.1

6.0 × 10−7

3.98–81.73

4

10.8

0.12

0.77–11.96

1

2.7

0.36

0.00–22.20

Leiomyosarcoma

51

11

21.6

1.4 × 10−4

1.96–12.16

3

5.9

0.01

1.35–29.40

2

3.9

0.19

0.00–4.16

  1. Eleven mitotically active leiomyomas with increased cellularity were included in both mitotically active and cellular/highly cellular leiomyoma subtypes for statistical testing