Table 1 Tumour-specific variant counts and mutation rates.

From: Whole-exome sequencing in eccrine porocarcinoma indicates promising therapeutic strategies

PID

SNV in target regions

Functional SNV

INDEL in target regions

Functional INDEL

Mutation frequency/Mb**

Functional mutation frequency/Mb**

C000-EXKBCS

2265

1488

1

1

63,47

41,71

C000-6KNGDL

2241

1434

4

4

62,89

40,28

C000-HZGGV2

2185

1396

10

9

61,46

39,38

C000-RCWM1J

2176

1361

4

4

61,06

38,24

C000-X88E7Z

1576

1066

5

5

44,29

30,00

C000-ESMKCH

1468

947

0

0

41,12

26,53

C000-CFLP5N

923

640

0

0

25,85

17,93

C000-ZZP8UU

887

621

0

0

24,85

17,39

C000-2SXE39

590

437

24

23

17,17

12,91

C000-S5ZHWR

415

293

2

2

11,68

8,26

C000-JMUDMJ

354

247

1

1

9,94

6,95

C000-648QQH

90

63

0

0

2,52

1,76

C000-W91YB6

30

20

0

0

0,84

0,56

C000-AX1WLG

13

11

0

0

0,36

0,31

Total

15213

10024

51

49

  

Median

905

630,5

1

1

25,35

17,66

  1. *Including variants outside target regions.
  2. **Per Mb of target sequence (35.7 Mb).