| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 7 | g.55086995A>C | CA15509099 | EGFR | n.279-55291A>C c.89-55291A>C (n.89-55291A>C) n.216-32061A>C c.88+67630A>C (n.88+67630A>C) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 7 | g.55086995A>G | CA1708875135 | EGFR | n.279-55291A>G c.89-55291A>G (n.89-55291A>G) n.216-32061A>G c.88+67630A>G (n.88+67630A>G) | dbSNP |
| 7 | g.55086995A>T | CA839866074 | EGFR | n.279-55291A>T c.89-55291A>T (n.89-55291A>T) n.216-32061A>T c.88+67630A>T (n.88+67630A>T) | dbSNP gnomAD v3 gnomAD v4 |