Table 1 Clinical and genetic feature of the 16 patients with ChG

From: A recurrent point mutation in PRKCA is a hallmark of chordoid gliomas

ID

Group

Sex

Age at surgery

WES

RNA-Seq

WES

Sanger PRKCAD463H

Sanger PRKCAD294

      

PRKCA 463

DNA

cDNA

DNA

1075

1

M

42

1

1

mut-CAT

1

1

0

2123

1

F

55

1

1

mut-CAT

0

1

0

4984

1

M

39

1

1

mut-CAT

1

1

0

5441

1

M

33

1

1

mut-CAT

1

1

0

2279

2

F

45

1

1

mut-CAT

1

1

0

4983

2

M

42

1

1

mut-CAT

1

1

0

4988

2

M

46

1

1

mut-CAT

1

1

0

4990

2

M

65

1

1

mut-CAT

1

1

0

5135

2

M

60

1

1

mut-CAT

1

1

0

5220

2

F

68

1

1

mut-CAT

1

1

0

4985

3

M

63

0

0

ND

1

NA

0

4986

3

F

56

0

0

ND

1

1

0

4989

3

F

71

0

0

ND

0

NA

0

4991

3

F

34

0

0

ND

1

NA

0

4782

3

F

27

0

0

ND

1

1

0

9064

3

F

44

0

0

ND

1

NA

0