| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 5 | g.1294456C>T | CA343461 | TERT | c.430G>A (p.Val144Met) n.488G>A n.509G>A | ClinVar dbSNP gnomAD v4 |
| 5 | g.1294456C= | CA1522558192 | TERT | c.430G= (p.Val144=) n.488G= n.509G= | dbSNP |
| 5 | g.1294456C>G | CA359058050 | TERT | c.430G>C (p.Val144Leu) n.488G>C n.509G>C | dbSNP gnomAD v4 |