Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
19 | g.1105456C>T | CA9037260 | GPX4 | c.381C>T (p.Tyr127=) c.189C>T (p.Tyr63=) c.264C>T (p.Tyr88=) c.-115C>T (n.-115C>T) c.270C>T (p.Tyr90=) c.3C>T (p.Tyr1=) c.150C>T (p.Tyr50=) n.204C>T n.216C>T c.375C>T (p.Tyr125=) c.267C>T (p.Tyr89=) c.378C>T (p.Tyr126=) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
19 | g.1105456C>A | CA163453 | GPX4 | c.381C>A (p.Tyr127Ter) c.189C>A (p.Tyr63Ter) c.264C>A (p.Tyr88Ter) c.-115C>A (n.-115C>A) c.270C>A (p.Tyr90Ter) c.3C>A (p.Tyr1Ter) c.150C>A (p.Tyr50Ter) n.204C>A n.216C>A c.375C>A (p.Tyr125Ter) c.267C>A (p.Tyr89Ter) c.378C>A (p.Tyr126Ter) | ClinVar dbSNP |