| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 12 | g.21842441G>A | CA260087 | ABCC9 | c.3346C>T (p.Arg1116Cys) n.923C>T c.*2444C>T (n.*2444C>T) n.2847C>T c.3295C>T (p.Arg1099Cys) c.2227C>T (p.Arg743Cys) c.3307C>T (p.Arg1103Cys) c.3205C>T (p.Arg1069Cys) c.2479C>T (p.Arg827Cys) | ClinVar dbSNP COSMIC COSMIC |
| 12 | g.21842441G= | CA2021312135 | ABCC9 | c.3346C= (p.Arg1116=) n.923C= c.*2444C= (n.*2444C=) n.2847C= c.3295C= (p.Arg1099=) c.2227C= (p.Arg743=) c.3307C= (p.Arg1103=) c.3205C= (p.Arg1069=) c.2479C= (p.Arg827=) | dbSNP |
| 12 | g.21842441G>C | CA384141001 | ABCC9 | c.3346C>G (p.Arg1116Gly) n.923C>G c.*2444C>G (n.*2444C>G) n.2847C>G c.3295C>G (p.Arg1099Gly) c.2227C>G (p.Arg743Gly) c.3307C>G (p.Arg1103Gly) c.3205C>G (p.Arg1069Gly) c.2479C>G (p.Arg827Gly) | ClinVar dbSNP |