| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 7 | g.55154050A>T | CA367577671 | EGFR | c.628A>T (p.Thr210Ser) n.977A>T c.787A>T (p.Thr263Ser) c.652A>T (p.Thr218Ser) c.89-1780A>T (n.89-1780A>T) | dbSNP |
| 7 | g.55154050A>G | CA367577670 | EGFR | c.628A>G (p.Thr210Ala) n.977A>G c.787A>G (p.Thr263Ala) c.652A>G (p.Thr218Ala) c.89-1780A>G (n.89-1780A>G) | dbSNP gnomAD v2 gnomAD v4 |
| 7 | g.55154050A>C | CA16602663 | EGFR | c.628A>C (p.Thr210Pro) n.977A>C c.787A>C (p.Thr263Pro) c.652A>C (p.Thr218Pro) c.89-1780A>C (n.89-1780A>C) | ClinVar dbSNP |