| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 3 | g.24127694C>T | CA122467 | THRB | c.949G>A (p.Ala317Thr) c.*1578G>A (n.*1578G>A) c.994G>A (p.Ala332Thr) c.856G>A (p.Ala286Thr) | ClinVar dbSNP COSMIC |
| 3 | g.24127694C>A | CA351888893 | THRB | c.949G>T (p.Ala317Ser) c.*1578G>T (n.*1578G>T) c.994G>T (p.Ala332Ser) c.856G>T (p.Ala286Ser) | ClinVar dbSNP |