| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| X | g.49251734G>A | CA16621429 | FOXP3 | c.971C>T (p.Thr324Ile) c.1076C>T (p.Thr359Ile) c.1145C>T (p.Thr382Ile) c.995C>T (p.Thr332Ile) c.999C>T (p.Asp333=) c.926C>T (p.Thr309Ile) c.1295C>T (p.Thr432Ile) c.1094C>T (p.Thr365Ile) c.1331C>T (p.Thr444Ile) c.1022C>T (p.Thr341Ile) | ClinVar dbSNP |
| X | g.49251734G= | CA2428551408 | FOXP3 | c.971C= (p.Thr324=) c.1076C= (p.Thr359=) c.1145C= (p.Thr382=) c.995C= (p.Thr332=) c.999C= (p.Asp333=) c.926C= (p.Thr309=) c.1295C= (p.Thr432=) c.1094C= (p.Thr365=) c.1331C= (p.Thr444=) c.1022C= (p.Thr341=) | dbSNP |