| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 15 | g.66436825C>G | CA16042967 | MAP2K1 | c.305C>G (p.Pro102Arg) c.371C>G (p.Pro124Arg) c.291+1588C>G (n.291+1588C>G) n.807C>G n.882C>G | ClinVar dbSNP |
| 15 | g.66436825C>A | CA16602250 | MAP2K1 | c.305C>A (p.Pro102Gln) c.371C>A (p.Pro124Gln) c.291+1588C>A (n.291+1588C>A) n.807C>A n.882C>A | ClinVar dbSNP COSMIC |
| 15 | g.66436825C>T | CA279996 | MAP2K1 | c.305C>T (p.Pro102Leu) c.371C>T (p.Pro124Leu) c.291+1588C>T (n.291+1588C>T) n.807C>T n.882C>T | ClinVar dbSNP COSMIC |