Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
16 | g.50794311C>T | CA10590092 | CYLD,CYLD-AS2 | c.2569C>T (p.Gln857Ter) c.2560C>T (p.Gln854Ter) c.148C>T (p.Gln50Ter) c.18C>T c.2014C>T (p.Gln672Ter) c.2530C>T (p.Gln844Ter) n.2853C>T n.2450+7812G>A n.2687C>T n.4187+7812G>A c.1894C>T (p.Gln632Ter) n.2658C>T | ClinVar dbSNP |
16 | g.50794311C= | CA2221880709 | CYLD,CYLD-AS2 | c.2569C= (p.Gln857=) c.2560C= (p.Gln854=) c.148C= (p.Gln50=) c.18C= c.2014C= (p.Gln672=) c.2530C= (p.Gln844=) n.2853C= n.2450+7812G= n.2687C= n.4187+7812G= c.1894C= (p.Gln632=) n.2658C= | dbSNP |