| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 5 | g.56856683T>G | CA128976 | MAP3K1 | c.566T>G (p.Leu189Arg) c.188T>G (p.Leu63Arg) c.311T>G (p.Leu104Arg) c.155T>G (p.Leu52Arg) c.77T>G (p.Leu26Arg) n.597T>G | ClinVar dbSNP |
| 5 | g.56856683T>C | CA128975 | MAP3K1 | c.566T>C (p.Leu189Pro) c.188T>C (p.Leu63Pro) c.311T>C (p.Leu104Pro) c.155T>C (p.Leu52Pro) c.77T>C (p.Leu26Pro) n.597T>C | ClinVar dbSNP |
| 5 | g.56856683T>A | CA359802147 | MAP3K1 | c.566T>A (p.Leu189Gln) c.188T>A (p.Leu63Gln) c.311T>A (p.Leu104Gln) c.155T>A (p.Leu52Gln) c.77T>A (p.Leu26Gln) n.597T>A | ClinVar dbSNP |