Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
X | g.101375188T>G | CA255799 | BTK | n.257A>C c.97A>C (p.Thr33Pro) n.410A>C n.214A>C c.199A>C (p.Thr67Pro) | ClinVar dbSNP |
X | g.101375188T>A | CA413939445 | BTK | n.257A>T c.97A>T (p.Thr33Ser) n.410A>T n.214A>T c.199A>T (p.Thr67Ser) | dbSNP |
X | g.101375188T= | CA2448289887 | BTK | n.257A= c.97A= (p.Thr33=) n.410A= n.214A= c.199A= (p.Thr67=) | dbSNP |