| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 3 | g.24127696C>T | CA122491 | THRB | c.947G>A (p.Arg316His) c.*1576G>A (n.*1576G>A) c.992G>A (p.Arg331His) c.854G>A (p.Arg285His) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 3 | g.24127696C= | CA1351825357 | THRB | c.947G= (p.Arg316=) c.*1576G= (n.*1576G=) c.992G= (p.Arg331=) c.854G= (p.Arg285=) | dbSNP |