| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 16 | g.50787852G>A | CA10590082 | CYLD,CYLD-AS2 | c.2108G>A (p.Arg703Lys) c.2099G>A (p.Arg700Lys) c.1553G>A (p.Arg518Lys) c.2069G>A (p.Arg690Lys) n.2392G>A n.2451-3663C>T n.2226G>A n.4188-3663C>T c.1433G>A (p.Arg478Lys) n.2197G>A | ClinVar dbSNP gnomAD v4 |
| 16 | g.50787852G= | CA2221875781 | CYLD,CYLD-AS2 | c.2108G= (p.Arg703=) c.2099G= (p.Arg700=) c.1553G= (p.Arg518=) c.2069G= (p.Arg690=) n.2392G= n.2451-3663C= n.2226G= n.4188-3663C= c.1433G= (p.Arg478=) n.2197G= | dbSNP |