| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 19 | g.4110558T>G | CA403391401 | MAP2K2 | n.840A>C c.401A>C (p.Tyr134Ser) c.110A>C (p.Tyr37Ser) n.598A>C | dbSNP |
| 19 | g.4110558T>A | CA403391400 | MAP2K2 | n.840A>T c.401A>T (p.Tyr134Phe) c.110A>T (p.Tyr37Phe) n.598A>T | dbSNP |
| 19 | g.4110558T>C | CA180890 | MAP2K2 | n.840A>G c.401A>G (p.Tyr134Cys) c.110A>G (p.Tyr37Cys) n.598A>G | ClinVar dbSNP gnomAD v4 COSMIC COSMIC |
| 19 | g.4110558T= | CA2319230179 | MAP2K2 | n.840A= c.401A= (p.Tyr134=) c.110A= (p.Tyr37=) n.598A= | dbSNP |