Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
3 | g.189868597G>A | CA340599 | TP63 | c.1010G>A (p.Arg337Gln) c.728G>A (p.Arg243Gln) c.473G>A (p.Arg158Gln) n.834G>A c.959G>A (p.Arg320Gln) c.1007G>A (p.Arg336Gln) c.1004G>A (p.Arg335Gln) c.971G>A (p.Arg324Gln) | ClinVar dbSNP COSMIC |
3 | g.189868597G>C | CA355755125 | TP63 | c.1010G>C (p.Arg337Pro) c.728G>C (p.Arg243Pro) c.473G>C (p.Arg158Pro) n.834G>C c.959G>C (p.Arg320Pro) c.1007G>C (p.Arg336Pro) c.1004G>C (p.Arg335Pro) c.971G>C (p.Arg324Pro) | dbSNP |