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 |