Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
11 | g.72225019dup | CA10581438 | INPPL1 | c.35dup (p.Ala13ArgfsTer?) c.-87dup (n.-87dup) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
11 | g.72225019del | CA600242957 | INPPL1 | c.35del (p.Gly12AlafsTer15) c.35del (p.Gly12AlafsTer?) c.-87del (n.-87del) | dbSNP gnomAD v2 gnomAD v4 |