| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| X | g.49251702T>C | CA16043289 | FOXP3 | c.1003A>G (p.Met335Val) c.1108A>G (p.Met370Val) c.1177A>G (p.Met393Val) c.1027A>G (p.Met343Val) c.*23A>G (n.*23A>G) c.958A>G (p.Met320Val) c.1327A>G (p.Met443Val) c.1126A>G (p.Met376Val) c.1363A>G (p.Met455Val) c.1054A>G (p.Met352Val) | ClinVar dbSNP |
| X | g.49251702T= | CA2428551400 | FOXP3 | c.1003A= (p.Met335=) c.1108A= (p.Met370=) c.1177A= (p.Met393=) c.1027A= (p.Met343=) c.*23A= (n.*23A=) c.958A= (p.Met320=) c.1327A= (p.Met443=) c.1126A= (p.Met376=) c.1363A= (p.Met455=) c.1054A= (p.Met352=) | dbSNP |