| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 11 | g.89178225G>A | CA261236 | TYR | c.272G>A (p.Cys91Tyr) n.333G>A n.2718-64692C>T n.2733-64692C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 11 | g.89178225G>T | CA382034038 | TYR | c.272G>T (p.Cys91Phe) n.333G>T n.2718-64692C>A n.2733-64692C>A | ClinVar dbSNP COSMIC |
| 11 | g.89178225G= | CA1989919708 | TYR | c.272G= (p.Cys91=) n.333G= n.2718-64692C= n.2733-64692C= | dbSNP |