Table 1

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

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


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

Jonsson et al. BMC Medical Genomics 2010 3:10   doi:10.1186/1755-8794-3-10

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