Table 2 Clinical characteristics and variants information of patients with pathogenic or likely pathogenic mutations.

From: The role of genetics in neurodegenerative dementia: a large cohort study in South China

Genes

Base change

Protein change

No. of cases

Reported and references

Gender

AAO (ys)

APOE genotype

Family history

Clinical phenotypes

Clinical diagnosis

Memory decline

Language impairment

Mental and behavior change

Sensory and movement disorders

PSEN1

c.250A>G

p.M84V

1

Y63

M

53

3/4

+

+

+

+

+

AD

c.415A>G

p.M139V

1

Y64

M

53

2/3

+

+

+

+

AD

c.415A>T

p.M139L

1

Y65

F

38

4/4

+

+

+

AD

c.424G>A

p.V142I

2

Y66

M/M

54/52

3/3

+/+

+/+

+/−

−/+

−/−

AD

c.436A>G

p.M146V

1

Y64

M

42

3/4

+

+

+

+

AD

c.451G>A

p.V151M

1

N

M

49

3/4

+

+

+

+

AD

c.519G>T

p.L173F

1

Y67

F

37

3/4

+

+

+

AD

c.604A>T

p.I202F

1

Y68

F

46

3/4

+

+

+

AD

c.617G>A

p.G206D

1

Y69

M

38

3/3

+

+

+

AD

c.677T>G

p.L226R

1

Y70

M

44

3/4

+

+

+

AD

c.679A>C

p.I227L

1

N

M

44

3/4

+

AD

c.697A>G

p.M233V

1

Y71

M

30

3/3

+

+

+

AD

c.791C>T

p. P264L

2

Y72

M/F

51/52

3/4

+/−

+/+

+/+

+/−

+/−

AD

c.806G>A

p.R269H

2

Y73

M/F

45/60

3/4

+/+

+/+

+/−

−/−

−/−

AD

c.845T>G

p.L282R

1

Y74

F

52

3/3

+

+

+

+

AD

c.854C>T

p.A285V

1

Y75

F

46

3/3

+

+

+

AD

c.1139A>G

p.K380R

1

N

F

49

3/4

+

+

AD

c.1174C>G

p.L392V

1

Y76

F

46

3/3

+

+

+

AD

c.1369A>G

p.M457V

1

N

M

66

3/4

+

+

+

AD

PSEN2

c.715A>G

p.M239V

4

Y77

M/M/F/F

47/60/53/45

50% 3/3

50% 3/4

+/+/+/+

+/+/+/+

−/−/+/−

−/+/+/+

−/−/−/+

AD

c.716T>C

p.M239T

1

N

F

50

3/4

+

AD

c.717G>A

p.M239I

1

Y32

F

50

3/4

+

+

+

AD

c.1180delG

p.A394Pfs*8

1

N

F

68

3/3

+

+

+

AD

APP

c.2143G>A

p.V715M

1

Y78

F

51

3/3

+

+

+

AD

c.2149G>A

p.V717I

3

Y79

F/F/M

47/49/42

66.7% 3/3; 33.3% 3/4

+/+/+

+/+/+

+/+/+

−/+/+

−/−/−

AD

MAPT

c.1788T>G

p.N596K

1

Y80

F

42

3/3

+

+

FTD

c.1907C>T

p.P636L

1

Y81

M

58

3/3

+

+

+

FTD

GRN

c.20G>A

p.W7*

1

N

F

73

3/4

+

+

+

FTD

c.328C>T

p.R110*

1

Y82

F

61

3/3

+

+

+

FTD

CHCHD10

c.283C>T

p.Q95*

1

N

F

52

3/4

+

+

+

+

+

AD

c.121C>T

p.Q41*

1

N

F

56

3/4

+

+

FTD

HTRA1

c.589C>T

p.R197*

1

Y83

F

49

3/3

+

+

AD

OPTN

c.1402_1407del

p.468_469del

1

N

F

63

3/3

+

+

FTD

SQSTM1

c.558_559insC

p.V287Rfs*21

1

N

F

71

3/3

+

+

FTD

VCP

c.475C>T

p.R159C

1

Y84

M

51

3/3

+

+

FTD

SIGMAR1

c.26G>A

p.W9*

1

N

F

74

3/3

+

+

FTD

TBK1

c.973dup

p.Y325Lfs*4

1

N

M

61

3/3

+

+

+

FTD

C9orf72

Hexanucleotide expansion

1

Y

F

57

3/4

+

+

+

+

FTD

HTT

CAG repeat expansion

1

Y

F

43

3/3

+

+

+

+

HD

  1. Y mutations have been reported previously, N mutations have not been reported previously.