| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 3 | g.24127649C>T | CA122469 | THRB | c.994G>A (p.Gly332Arg) c.*1623G>A (n.*1623G>A) c.1039G>A (p.Gly347Arg) c.901G>A (p.Gly301Arg) c.973+21G>A (n.973+21G>A) | ClinVar dbSNP |
| 3 | g.24127649C= | CA1351825337 | THRB | c.994G= (p.Gly332=) c.*1623G= (n.*1623G=) c.1039G= (p.Gly347=) c.901G= (p.Gly301=) c.973+21G= (n.973+21G=) | dbSNP |
| 3 | g.24127649C>G | CA351888796 | THRB | c.994G>C (p.Gly332Arg) c.*1623G>C (n.*1623G>C) c.1039G>C (p.Gly347Arg) c.901G>C (p.Gly301Arg) c.973+21G>C (n.973+21G>C) | dbSNP |