Table 2 Significantly mutated genes in the 102 ICC patients.

From: Mutational landscape of intrahepatic cholangiocarcinoma

Gene

P -value FCPT *

Cases with mutations

Non-silent mutations

Synonymous mutations

d N /d S

TP53

0.00E+00

39

42

1

42:1

KRAS

0.00E+00

17

17

0

17:0

MT-ND4

9.78E-12

9

9

1

9:1

MT-ND5

5.48E-10

9

9

2

9:2

IDH1

2.54E-06

5

5

0

5:0

MT-CO1

6.01E-06

6

7

3

7:3

PTEN

3.34E-05

6

7

0

7:0

ARID1A

1.81E-04

7

8

1

8:1

MT-ND6

4.27E-04

4

4

2

4:2

LCE1F

6.31E-04

3

3

0

3:0

MT-CO3

6.50E-04

4

5

0

5:0

RB1

1.09E-03

5

5

0

5:0

GOLGA6L2

1.17E-03

5

8

11

8:11

EPHA4

7.28E-03

4

4

0

4:0

EPPK1

7.43E-03

6

6

1

6:1

SMAD4

9.55E-03

4

4

0

4:0

CDH18

1.27E-02

3

5

0

5:0

MT-ND1

1.49E-02

3

3

2

3:2

ALB

1.81E-02

3

3

1

3:1

FAM182B

2.00E-02

2

3

3

3:3

ECE2

2.17E-02

4

4

0

4:0

TDRD1

3.29E-02

4

5

0

5:0

GRIA1

3.53E-02

3

4

2

4:2

CNTNAP5

3.55E-02

3

4

2

4:2

FYN

4.47E-02

3

3

0

3:0

  1. FCPT, Fisher’s combined P-value test; ICC, intrahepatic cholangiocarcinoma.
  2. Genes whose names are in bold show significantly higher non-synonymous/synonymous ratio.
  3. *FCPT by Genome-MuSiC.
  4. Excluding variations in dbSNP and 1000Genome Project (unless they are in COSMIC database).