Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
10 | g.8073787C>A | CA468400717 | GATA3 | c.1096C>A (p.Arg366=) c.1099C>A (p.Arg367=) n.618C>A | dbSNP |
10 | g.8073787C>T | CA126736 | GATA3 | c.1096C>T (p.Arg366Ter) c.1099C>T (p.Arg367Ter) n.618C>T | ClinVar dbSNP COSMIC |
10 | g.8073787C>G | CA375975472 | GATA3 | c.1096C>G (p.Arg366Gly) c.1099C>G (p.Arg367Gly) n.618C>G | dbSNP |