Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
1 | g.155659923C>G | CA342764186 | YY1AP1 | c.1987G>C (p.Glu663Gln) c.2125G>C (p.Glu709Gln) c.1894G>C (p.Glu632Gln) c.*1251G>C (n.*1251G>C) c.1954G>C (p.Glu652Gln) c.*1485G>C (n.*1485G>C) c.2401G>C (p.Glu801Gln) c.2341G>C (p.Glu781Gln) c.1927G>C (p.Glu643Gln) c.*1996G>C (n.*1996G>C) n.2031G>C n.323G>C c.*930G>C (n.*930G>C) c.1789G>C (p.Glu597Gln) c.2185G>C (p.Glu729Gln) | dbSNP |
1 | g.155659923C>A | CA16044406 | YY1AP1 | c.1987G>T (p.Glu663Ter) c.2125G>T (p.Glu709Ter) c.1894G>T (p.Glu632Ter) c.*1251G>T (n.*1251G>T) c.1954G>T (p.Glu652Ter) c.*1485G>T (n.*1485G>T) c.2401G>T (p.Glu801Ter) c.2341G>T (p.Glu781Ter) c.1927G>T (p.Glu643Ter) c.*1996G>T (n.*1996G>T) n.2031G>T n.323G>T c.*930G>T (n.*930G>T) c.1789G>T (p.Glu597Ter) c.2185G>T (p.Glu729Ter) | ClinVar dbSNP |