| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 3 | g.24123122C>T | CA122513 | THRB | c.1148G>A (p.Arg383His) c.*1777G>A (n.*1777G>A) c.1193G>A (p.Arg398His) c.1055G>A (p.Arg352His) c.977G>A (p.Arg326His) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 3 | g.24123122C= | CA1351822310 | THRB | c.1148G= (p.Arg383=) c.*1777G= (n.*1777G=) c.1193G= (p.Arg398=) c.1055G= (p.Arg352=) c.977G= (p.Arg326=) | dbSNP |