| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 7 | g.55191720G>C | CA367580064 | EGFR | c.2312G>C (p.Gly771Ala) c.820G>C c.2471G>C (p.Gly824Ala) c.*28+18792G>C (n.*28+18792G>C) c.2336G>C (p.Gly779Ala) c.1670G>C (p.Gly557Ala) | dbSNP |
| 7 | g.55191720G>T | CA367580063 | EGFR | c.2312G>T (p.Gly771Val) c.820G>T c.2471G>T (p.Gly824Val) c.*28+18792G>T (n.*28+18792G>T) c.2336G>T (p.Gly779Val) c.1670G>T (p.Gly557Val) | dbSNP |
| 7 | g.55191720G>A | CA151169 | EGFR | c.2312G>A (p.Gly771Asp) c.820G>A c.2471G>A (p.Gly824Asp) c.*28+18792G>A (n.*28+18792G>A) c.2336G>A (p.Gly779Asp) c.1670G>A (p.Gly557Asp) | ClinVar dbSNP ExAC gnomAD v2 |