Table 1.
NRXN1 Coding-Sequence Variants in ASD Screening Cohort
| Exon | Alteration | Codon | SNP |
ASD |
non-ASDa |
|---|---|---|---|---|---|
| rs Number | Variant Alleles/Total Chromosomes | Variant Alleles/Total Chromosomes | |||
| 2 | c.53T > A | p.L18Q | – | 1/114 | 0/468 |
| 2 | c.105C > A | p.G35 | – | 1/112 | 0/466 |
| 2 | c.511C > T | p.L171 | rs1045874 | 44/114 | N.D. |
| 5 | c.912C > T | p.G304 | – | 1/114 | 0/464 |
| 7 | c.999C > T | p.P333 | rs2303298 | 3/114 | 3/458 |
| 11 | c.2242C > A | p.L748I | – | 1/114 | 0/476 |
| 16 | c.3165C > T | p.A1055 | – – | 1/114 | 0/462 |
| 22 | c.3975C > T | p.G1325 | – | 1/114 | 0/462 |
| 24 | c.4374A > G | p.P1458 | – | 1/114 | 0/464 |
a
OCD, TS, and unaffected controls.