| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 16 | g.89694721C>T | CA397424281 | CDK10 | c.725C>T (p.Thr242Ile) c.584C>T (p.Thr195Ile) n.1512C>T c.512C>T (p.Thr171Ile) n.817C>T c.*523C>T (n.*523C>T) c.608C>T (p.Thr203Ile) c.50-210C>T n.695C>T c.821C>T (p.Thr274Ile) c.710C>T (p.Thr237Ile) n.2742C>T n.674C>T | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 16 | g.89694721C>G | CA16609537 | CDK10 | c.725C>G (p.Thr242Ser) c.584C>G (p.Thr195Ser) n.1512C>G c.512C>G (p.Thr171Ser) n.817C>G c.*523C>G (n.*523C>G) c.608C>G (p.Thr203Ser) c.50-210C>G n.695C>G c.821C>G (p.Thr274Ser) c.710C>G (p.Thr237Ser) n.2742C>G n.674C>G | ClinVar dbSNP |