Table 1 Reported SNCA missense mutations in familial and sporadic Parkinson’s disease among various ethnicities

From: Resequencing the complete SNCA locus in Indian patients with Parkinson’s disease

SNCA mutation

Region of origin

Ethnicity

Familial/sporadic PD

Reference

p.Ala53Thr

Italian, Greek, Finnish

European

familial

6,9,33

p.Glu46Lys

Spanish

European

familial

7

p.Ala30Pro

German

European

familial

8

p.Ala30Gly

Greek

European

familial

10

p.Thr72Met

Turkish

Turkish

familial

23

p.His50Gln

English–Welsh, English

European

familial, sporadic

11,12

p.G51D

French

European

familial

14

p.M5T

Chinese

Chinese

familial

18

p.Val15Asp

Chinese

Chinese

sporadic

25

p.Met127Ile

Chinese

Chinese

sporadic

25

p.A53V

Chinese

Chinese

sporadic

15

p.P117S

Chinese

Chinese

sporadic

15

p.A18T

Polish

European

sporadic

26

p.A29S

Polish

European

sporadic

26