Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
16 | g.50792627C>T | CA158237 | CYLD,CYLD-AS2 | c.2272C>T (p.Arg758Ter) c.2263C>T (p.Arg755Ter) c.1717C>T (p.Arg573Ter) c.2233C>T (p.Arg745Ter) n.2556C>T n.2451-8438G>A n.2390C>T n.4188-8438G>A c.1597C>T (p.Arg533Ter) n.2361C>T | ClinVar dbSNP COSMIC |
16 | g.50792627C= | CA2221879034 | CYLD,CYLD-AS2 | c.2272C= (p.Arg758=) c.2263C= (p.Arg755=) c.1717C= (p.Arg573=) c.2233C= (p.Arg745=) n.2556C= n.2451-8438G= n.2390C= n.4188-8438G= c.1597C= (p.Arg533=) n.2361C= | dbSNP |