Table 4 38 SNP list
From: A new and spontaneous animal model for ankylosing spondylitis is found in cynomolgus monkeys
Chromosome | Position | Gene | Type | Reference | Son | Mum |
|---|---|---|---|---|---|---|
1 | 1215288918 | LOC102136658 | Missense variant | C | T | *,T |
1 | 168420059 | DIEXF | Missense variant | A | C | C,T |
3 | 1175485315 | LOC102131469 | Missense variant | A | C | C,T |
3 | 1175880743 | LOC102131469 | Missense variant | T | A | A,G |
3 | 1177214755 | LOC102128920 | Missense variant | A | C | *,C |
3 | 1192009442 | VIPR2 | Missense variant | C | G | G,T |
3 | 128778926 | LOC102131469 | Missense variant | T | G | TTTG,G |
3 | 129229344 | LOC102131469 | Missense variant | A | G | *,G |
4 | 111102645 | SOD2 | Missense variant | A | G | C,G |
4 | 1138903304 | CFB | Missense variant | G | T | *,T |
4 | 1141429218 | LOC102129714 | Missense variant | C | T | A,T |
4 | 1168015542 | LOC107129646 | Missense variant | A | T | G,T |
5 | 165508494 | LOC102126139 | Missense variant | T | G | A,G |
5 | 1972800 | SLC26A1 | Missense variant | C | T | G,T |
6 | 1135164413 | RUBCN | Missense variant | A | C | *,C |
6 | 1180619461 | SCGB3A1 | Missense variant | C | G | *,G |
7 | 1135135117 | LOC102118143 | Missense variant | C | G | G,T |
7 | 1135882110 | LOC102127558 | Missense variant | C | G | G,A |
7 | 1170188487 | ZBTB42 | Missense variant | C | G | G,* |
7 | 156240664 | LOC102126566 | Missense variant | C | T | *,T |
7 | 157176892 | LOC102147189 | Missense variant | C | A | A,T |
8 | 122246303 | NUDT18 | Missense variant | A | G | C,G |
9 | 139668835 | LOC102143735 | Missense variant | T | A | G,A |
9 | 1708235 | TUBB8 | Missense variant | T | G | C,G |
10 | 1197740 | ARSA | Missense variant | T | C | C,G |
10 | 178143092 | LOC102125072 | Missense variant | C | T | T,* |
11 | 111981753 | LOC107126647 | Missense variant | G | T | *,T |
13 | 115107917 | LOC107127060 | Missense variant | T | G | A,G |
14 | 1120156195 | LOC102147067 | Missense variant | T | G | *,G |
19 | 112305239 | ZNE433 | Missense variant | T | A | A,G |
19 | 13139328 | GNA15 | Missense variant | T | G | A,G |
19 | 13710621 | LOC102134537 | Missense variant | T | G | G,* |
19 | 140352252 | FCGBP | Missense variant | C | A | G |
19 | 155499885 | LOC102143631 | Missense variant | C | T | T,A |
19 | 155567454 | LILRB4 | Missense variant | C | T | A,T |
19 | 155612771 | LOC102144021 | Missense variant | C | G | G,T |
Scaffold 2511 | 1344 | LOC102114865 | Missense variant | C | G | G,A |
Scaffold 26 | 1176274 | LOC107128638 | Missense variant | T | G | C,G |