Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
7 | g.55154128_55154129delinsAA | CA16602835 | EGFR | c.706_707delinsAA (p.Ala236Asn) n.1055_1056delinsAA c.865_866delinsAA (p.Ala289Asn) c.730_731delinsAA (p.Ala244Asn) c.89-1702_89-1701delinsAA (n.89-1702_89-1701delinsAA) | ClinVar dbSNP |
7 | g.55154128_55154129delinsAT | CA16602836 | EGFR | c.706_707delinsAT (p.Ala236Ile) n.1055_1056delinsAT c.865_866delinsAT (p.Ala289Ile) c.730_731delinsAT (p.Ala244Ile) c.89-1702_89-1701delinsAT (n.89-1702_89-1701delinsAT) | ClinVar dbSNP |