Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
10 | g.6019463dup | CA10602390 | IL2RA | c.404dup (p.Thr136AspfsTer?) c.620dup (p.Thr208AspfsTer?) c.692dup (p.Thr232AspfsTer?) n.507dup c.665dup (p.Thr223AspfsTer?) c.476dup (p.Thr160AspfsTer?) c.316dup | ClinVar dbSNP |
10 | g.6019463T= | CA3174154837 | IL2RA | c.404A= (p.Glu135=) c.620A= (p.Glu207=) c.692A= (p.Glu231=) n.507A= c.665A= (p.Glu222=) c.476A= (p.Glu159=) c.316A= | dbSNP |