| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 2 | g.211702102C>A | CA350442465 | ERBB4 | c.1354G>T (p.Glu452Ter) c.1276G>T (p.Glu426Ter) c.1353G>T c.1177G>T (p.Glu393Ter) n.1406G>T c.1432G>T (p.Glu478Ter) c.733G>T (p.Glu245Ter) | dbSNP |
| 2 | g.211702102C>T | CA16602262 | ERBB4 | c.1354G>A (p.Glu452Lys) c.1276G>A (p.Glu426Lys) c.1353G>A c.1177G>A (p.Glu393Lys) n.1406G>A c.1432G>A (p.Glu478Lys) c.733G>A (p.Glu245Lys) | ClinVar dbSNP gnomAD v4 COSMIC |
| 2 | g.211702102C= | CA1325614791 | ERBB4 | c.1354G= (p.Glu452=) c.1276G= (p.Glu426=) c.1353G= c.1177G= (p.Glu393=) n.1406G= c.1432G= (p.Glu478=) c.733G= (p.Glu245=) | dbSNP |