| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 19 | g.4110583T>G | CA403391510 | MAP2K2 | n.815A>C c.376A>C (p.Asn126His) c.85A>C (p.Asn29His) n.573A>C | ClinVar dbSNP gnomAD v4 |
| 19 | g.4110583T>C | CA16602631 | MAP2K2 | n.815A>G c.376A>G (p.Asn126Asp) c.85A>G (p.Asn29Asp) n.573A>G | ClinVar dbSNP COSMIC COSMIC |