| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 3 | g.133775570C>T | CA211198 | TF | c.1825C>T (p.Arg609Trp) c.556C>T n.2819C>T c.1693C>T (p.Arg565Trp) c.1444C>T (p.Arg482Trp) | ClinVar dbSNP gnomAD v3 gnomAD v4 COSMIC |
| 3 | g.133775570C>A | CA2625419 | TF | c.1825C>A (p.Arg609=) c.556C>A n.2819C>A c.1693C>A (p.Arg565=) c.1444C>A (p.Arg482=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |