Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
16 | g.50792654A>T | CA10590086 | CYLD,CYLD-AS2 | c.2299A>T (p.Lys767Ter) c.2290A>T (p.Lys764Ter) c.1744A>T (p.Lys582Ter) c.2260A>T (p.Lys754Ter) n.2583A>T n.2451-8465T>A n.2417A>T n.4188-8465T>A c.1624A>T (p.Lys542Ter) n.2388A>T | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC |
16 | g.50792654A= | CA2221879075 | CYLD,CYLD-AS2 | c.2299A= (p.Lys767=) c.2290A= (p.Lys764=) c.1744A= (p.Lys582=) c.2260A= (p.Lys754=) n.2583A= n.2451-8465T= n.2417A= n.4188-8465T= c.1624A= (p.Lys542=) n.2388A= | dbSNP |