Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
11 | g.72229558G>C | CA10581439 | INPPL1 | c.753G>C (p.Gln251His) c.27G>C (p.Gln9His) c.555G>C (p.Gln185His) c.819G>C (p.Gln273His) c.789G>C (p.Gln263His) | ClinVar dbSNP COSMIC |
11 | g.72229558G= | CA1981897669 | INPPL1 | c.753G= (p.Gln251=) c.27G= (p.Gln9=) c.555G= (p.Gln185=) c.819G= (p.Gln273=) c.789G= (p.Gln263=) | dbSNP |