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 | |
p.Glu46Lys | Spanish | European | familial | |
p.Ala30Pro | German | European | familial | |
p.Ala30Gly | Greek | European | familial | |
p.Thr72Met | Turkish | Turkish | familial | |
p.His50Gln | English–Welsh, English | European | familial, sporadic | |
p.G51D | French | European | familial | |
p.M5T | Chinese | Chinese | familial | |
p.Val15Asp | Chinese | Chinese | sporadic | |
p.Met127Ile | Chinese | Chinese | sporadic | |
p.A53V | Chinese | Chinese | sporadic | |
p.P117S | Chinese | Chinese | sporadic | |
p.A18T | Polish | European | sporadic | |
p.A29S | Polish | European | sporadic |