| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 5 | g.1279392C>A | CA343428 | TERT | c.2029G>T (p.Gly677Cys) c.*1575G>T (n.*1575G>T) n.842G>T c.499G>T (p.Gly167Cys) c.385G>T (p.Gly129Cys) n.2087G>T n.2108G>T | ClinVar dbSNP gnomAD v4 |
| 5 | g.1279392C= | CA1522565536 | TERT | c.2029G= (p.Gly677=) c.*1575G= (n.*1575G=) n.842G= c.499G= (p.Gly167=) c.385G= (p.Gly129=) n.2087G= n.2108G= | dbSNP |