Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
22 | g.41117411C>G | CA411680290 | EP300 | c.319C>G (p.Gln107Glu) c.203C>G | dbSNP |
22 | g.41117411C>T | CA16621124 | EP300 | c.319C>T (p.Gln107Ter) c.203C>T | ClinVar dbSNP COSMIC |
22 | g.41117411C>A | CA411680289 | EP300 | c.319C>A (p.Gln107Lys) c.203C>A | dbSNP |