| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 2 | g.211713583C>T | CA16602255 | ERBB4 | c.949G>A (p.Glu317Lys) c.871G>A (p.Glu291Lys) c.948G>A c.772G>A (p.Glu258Lys) n.1001G>A c.1027G>A (p.Glu343Lys) c.328G>A (p.Glu110Lys) | ClinVar dbSNP |
| 2 | g.211713583C>A | CA350443725 | ERBB4 | c.949G>T (p.Glu317Ter) c.871G>T (p.Glu291Ter) c.948G>T c.772G>T (p.Glu258Ter) n.1001G>T c.1027G>T (p.Glu343Ter) c.328G>T (p.Glu110Ter) | dbSNP |
| 2 | g.211713583C= | CA1325620303 | ERBB4 | c.949G= (p.Glu317=) c.871G= (p.Glu291=) c.948G= c.772G= (p.Glu258=) n.1001G= c.1027G= (p.Glu343=) c.328G= (p.Glu110=) | dbSNP |