| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 5 | g.1294282C>T | CA122653 | TERT | c.604G>A (p.Ala202Thr) n.662G>A n.683G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 5 | g.1294282C= | CA1522557611 | TERT | c.604G= (p.Ala202=) n.662G= n.683G= | dbSNP |
| 5 | g.1294282C>G | CA359057216 | TERT | c.604G>C (p.Ala202Pro) n.662G>C n.683G>C | dbSNP |