| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 16 | g.89279188G>A | CA16620303 | ANKRD11 | c.7354C>T (p.Arg2452Cys) c.*7157C>T (n.*7157C>T) c.745-3997C>T (n.745-3997C>T) c.152-3997C>T n.529C>T c.7252C>T (p.Arg2418Cys) c.7057C>T (p.Arg2353Cys) c.7225C>T (p.Arg2409Cys) | ClinVar dbSNP COSMIC |
| 16 | g.89279188G>C | CA397148533 | ANKRD11 | c.7354C>G (p.Arg2452Gly) c.*7157C>G (n.*7157C>G) c.745-3997C>G (n.745-3997C>G) c.152-3997C>G n.529C>G c.7252C>G (p.Arg2418Gly) c.7057C>G (p.Arg2353Gly) c.7225C>G (p.Arg2409Gly) | ClinVar dbSNP gnomAD v4 |
| 16 | g.89279188G= | CA2241586573 | ANKRD11 | c.7354C= (p.Arg2452=) c.*7157C= (n.*7157C=) c.745-3997C= (n.745-3997C=) c.152-3997C= n.529C= c.7252C= (p.Arg2418=) c.7057C= (p.Arg2353=) c.7225C= (p.Arg2409=) | dbSNP |