| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 16 | g.89279362G>A | CA279648 | ANKRD11 | c.7180C>T (p.Gln2394Ter) c.*6983C>T (n.*6983C>T) c.745-4171C>T (n.745-4171C>T) c.152-4171C>T n.355C>T c.7078C>T (p.Gln2360Ter) c.6883C>T (p.Gln2295Ter) c.7051C>T (p.Gln2351Ter) | ClinVar dbSNP |
| 16 | g.89279362G= | CA2241586665 | ANKRD11 | c.7180C= (p.Gln2394=) c.*6983C= (n.*6983C=) c.745-4171C= (n.745-4171C=) c.152-4171C= n.355C= c.7078C= (p.Gln2360=) c.6883C= (p.Gln2295=) c.7051C= (p.Gln2351=) | dbSNP |