Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
16 | g.50791689A>G | CA214926 | CYLD,CYLD-AS2 | c.2240A>G (p.Glu747Gly) c.2231A>G (p.Glu744Gly) c.1685A>G (p.Glu562Gly) c.2201A>G (p.Glu734Gly) n.2524A>G n.2451-7500T>C n.2358A>G n.4188-7500T>C c.1565A>G (p.Glu522Gly) n.2329A>G | ClinVar dbSNP |
16 | g.50791689A= | CA2221878369 | CYLD,CYLD-AS2 | c.2240A= (p.Glu747=) c.2231A= (p.Glu744=) c.1685A= (p.Glu562=) c.2201A= (p.Glu734=) n.2524A= n.2451-7500T= n.2358A= n.4188-7500T= c.1565A= (p.Glu522=) n.2329A= | dbSNP |