Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
15 | g.66435145G>A | CA180743 | MAP2K1 | c.133G>A (p.Asp45Asn) c.199G>A (p.Asp67Asn) n.635G>A n.710G>A | ClinVar dbSNP gnomAD v4 COSMIC |
15 | g.66435145G>C | CA392929317 | MAP2K1 | c.133G>C (p.Asp45His) c.199G>C (p.Asp67His) n.635G>C n.710G>C | dbSNP |
15 | g.66435145G>T | CA392929318 | MAP2K1 | c.133G>T (p.Asp45Tyr) c.199G>T (p.Asp67Tyr) n.635G>T n.710G>T | dbSNP gnomAD v4 COSMIC |