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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.