| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 7 | g.55146655C>T | CA4265230 | EGFR | c.315C>T (p.Asn105=) n.664C>T c.474C>T (p.Asn158=) c.424+3167C>T (n.424+3167C>T) c.89-9175C>T (n.89-9175C>T) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 7 | g.55146655C>G | CA367576564 | EGFR | c.315C>G (p.Asn105Lys) n.664C>G c.474C>G (p.Asn158Lys) c.424+3167C>G (n.424+3167C>G) c.89-9175C>G (n.89-9175C>G) | ClinVar dbSNP |
| 7 | g.55146655C>A | CA367576563 | EGFR | c.315C>A (p.Asn105Lys) n.664C>A c.474C>A (p.Asn158Lys) c.424+3167C>A (n.424+3167C>A) c.89-9175C>A (n.89-9175C>A) | ClinVar dbSNP |