| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 3 | g.24127603C>T | CA122475 | THRB | c.1040G>A (p.Gly347Glu) c.*1669G>A (n.*1669G>A) c.1085G>A (p.Gly362Glu) c.947G>A (p.Gly316Glu) c.973+67G>A (n.973+67G>A) | ClinVar dbSNP |
| 3 | g.24127603C>G | CA351888703 | THRB | c.1040G>C (p.Gly347Ala) c.*1669G>C (n.*1669G>C) c.1085G>C (p.Gly362Ala) c.947G>C (p.Gly316Ala) c.973+67G>C (n.973+67G>C) | dbSNP |
| 3 | g.24127603C= | CA1351825307 | THRB | c.1040G= (p.Gly347=) c.*1669G= (n.*1669G=) c.1085G= (p.Gly362=) c.947G= (p.Gly316=) c.973+67G= (n.973+67G=) | dbSNP |