| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| X | g.101370051A>T | CA255801 | BTK | n.498T>A n.496T>A c.338T>A (p.Val113Asp) c.*183T>A (n.*183T>A) c.335T>A (p.Val112Asp) c.*87T>A (n.*87T>A) c.440T>A (p.Val147Asp) | ClinVar dbSNP |
| X | g.101370051A= | CA2448288252 | BTK | n.498T= n.496T= c.338T= (p.Val113=) c.*183T= (n.*183T=) c.335T= (p.Val112=) c.*87T= (n.*87T=) c.440T= (p.Val147=) | dbSNP |