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Table 2 Frequency of non-synonymous single-nucleotide variations in the OXTR gene detected by re-sequencing

From: Non-synonymous single-nucleotide variations of the human oxytocin receptor gene and autism spectrum disorders: a case–control study in a Japanese population and functional analysis

dbSNP-IDa

mRNAb

Allele

Amino acid

Amino acid

Number of cases

 

position

 

position

residue

ASD ( n= 59)

Control ( n= 30)

rs237908

19

T/G

7

S/A

T/T (0) T/G (0) G/G (59)

T/T (0) T/G (0) G/G (30)

rs237907

40

T/G

14

S/A

T/T (0) T/G (0) G/G (59)

T/T (0) T/G (0) G/G (30)

rs237906

46

T/G

16

S/A

T/T (0) T/G (0) G/G (59)

T/T (0) T/G (0) G/G (30)

rs189386

64

T/G

22

W/G

T/T (0) T/G (0) G/G (59)

T/T (0) T/G (0) G/G (30)

rs113718500

65

C/G

22

A/G

C/C (0) C/G (0) G/G (59)

C/C (0) C/G (0) G/G (30)

rs237903

86

T/C

29

V/A

T/T (0) T/C (0) C/C (59)

T/T (0) T/C (0) C/C (30)

rs171114

188

G/C

63

G/A

G/G (0) G/C (0) C/C (59)

G/G (0) G/C (0) C/C (30)

rs143644523

220

T/C

74

F/L

T/T (0) T/C (0) C/C (59)

T/T (0) T/C (0) C/C (30)

rs138770371

316

G/T

106

D/Y

G/G (0) G/T (0) T/T (59)

G/G (0) G/T (0) T/T (30)

rs115324487

515

C/T

172

A/V

C/C (0) C/T (0) T/T (59)

C/C (0) C/T (0) T/T (30)

rs150746704

616

G/C

206

V/L

G/G (0) G/C (0) C/C (59)

G/G (0) G/C (0) C/C (30)

rs4686302

652

A/G

218

T/A

A/A (3) A/G(12) G/G (34)

A/A (1) A/G(14) G/G (15)

rs143908202

661

A/G

221

S/G

A/A (0) A/G (0) G/G (59)

A/A (0) A/G (0) G/G (30)

rs145921539

684

T/G

228

C/W

T/T (0) T/G (0) G/G (59)

T/T (0) T/G (0) G/G (30)

rs184175311

700

G/A

234

E/K

G/G (0) G/A (0) A/A (59)

G/G (0) G/A (0) A/A (30)

rs61740241

712

A/G

238

T/A

A/A (0) A/G (0) G/G (59)

A/A (0) A/G (0) G/G (30)

rs151141371

755

C/G

252

A/G

C/C (0) C/G (0) G/G (59)

C/C (0) C/G (0) G/G (30)

rs139854982

760

T/C

254

C/R

T/T (0) T/C (0) C/C (59)

T/T (0) T/C (0) C/C (30)

rs144366756

764

G/T

255

G/V

G/G (0) G/T (0) T/T (59)

G/G (0) G/T (0) T/T (30)

rs237901

818

T/C

273

M/T

T/T (0) T/C (0) C/C (59)

T/T (0) T/C (0) C/C (30)

rs144814761

841

A/G

281

M/V

A/A (0) A/G (0) G/G (59)

A/A (0) A/G (0) G/G (30)

rs140488139

963

A/C

321

K/N

A/A (0) A/C (0) C/C (59)

A/A (0) A/C (0) C/C (30)

rs151257822

1001

A/G

334

D/G

A/A (0) A/G (0) G/G (59)

A/A (0) A/G (1) G/G (29)

rs143927655

1015

A/G

339

K/E

A/A (0) A/G (0) G/G (59)

A/A (0) A/G (0) G/G (30)

rs148899442

1100

G/A

367

S/N

G/G (0) G/A (0) A/A (59)

G/G (0) G/A (0) A/A (30)

rs144289031

1121

A/G

374

N/S

A/A (0) A/G (0) G/G (59)

A/A (0) A/G (0) G/G (30)

rs35062132

1126

G/C

376

G/R

G/G (0) G/C (2) C/C (57)

G/G (0) G/C (0) C/C (29)

rs35062132

1126

T/C

376

C/R

T/T (0) T/C (0) C/C (57)

T/T (0) T/C (1) C/C (29)

  1. aIDs are from dbSNP of the National Center for Biotechnology Information [40]. Bold IDs indicate the presence of allelic heterozygosity. bA of the ATG of the initial methionine is denoted nucleotide +1.