| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 1 | g.160823770A>G | CA1202003 | LY9 | c.1804A>G (p.Met602Val) c.929A>G c.1762A>G (p.Met588Val) c.1534A>G (p.Met512Val) c.1945A>G (p.Met649Val) c.1903A>G (p.Met635Val) c.1846A>G (p.Met616Val) c.1675A>G (p.Met559Val) c.1633A>G (p.Met545Val) c.1324A>G (p.Met442Val) c.1057A>G (p.Met353Val) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 1 | g.160823770A= | CA1139802766 | LY9 | c.1804A= (p.Met602=) c.929A= c.1762A= (p.Met588=) c.1534A= (p.Met512=) c.1945A= (p.Met649=) c.1903A= (p.Met635=) c.1846A= (p.Met616=) c.1675A= (p.Met559=) c.1633A= (p.Met545=) c.1324A= (p.Met442=) c.1057A= (p.Met353=) | dbSNP |