| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 11 | g.72233696T>A | CA130328 | INPPL1 | c.2164T>A (p.Phe722Ile) c.17T>A c.1438T>A (p.Phe480Ile) n.770T>A c.1966T>A (p.Phe656Ile) n.449T>A c.2230T>A (p.Phe744Ile) c.2362T>A (p.Phe788Ile) c.2332T>A (p.Phe778Ile) c.2296T>A (p.Phe766Ile) | ClinVar dbSNP |
| 11 | g.72233696T= | CA1981899640 | INPPL1 | c.2164T= (p.Phe722=) c.17T= c.1438T= (p.Phe480=) n.770T= c.1966T= (p.Phe656=) n.449T= c.2230T= (p.Phe744=) c.2362T= (p.Phe788=) c.2332T= (p.Phe778=) c.2296T= (p.Phe766=) | dbSNP |