| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| X | g.80026849C>T | CA121423 | TBX22 | c.779C>T (p.Thr260Met) c.*391C>T (n.*391C>T) n.658C>T c.419C>T (p.Thr140Met) c.782C>T (p.Thr261Met) | ClinVar dbSNP COSMIC |
| X | g.80026849C= | CA2439980778 | TBX22 | c.779C= (p.Thr260=) c.*391C= (n.*391C=) n.658C= c.419C= (p.Thr140=) c.782C= (p.Thr261=) | dbSNP |