Skip to main content

Table 1 Sequence variants identified in ASMT, MTNR1A, MTNR1B in patients with ASD.

From: Mutation screening of melatonin-related genes in patients with autism spectrum disorders

Gene

Location/

nucleotide change

Amino acid change

Cases

(n = 109)

Controls

(n = 188)

ASMT

c.-376G>A

-

1

1

ASMT

c.-38C>T

-

1

0

ASMT

IVS5+2T>C

-

1

0

MTNR1A

c.-158C>T

-

1

0

MTNR1B

c.370G>A

V124I*

1

0

MTNR1B

c.-39GC>AA

-

1

0

  1. * Predicted not to have any major effect on protein function, as assessed by Polyphen and SIFT.