| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 4 | g.186288496G>C | CA121769 | F11,F11-AS1 | c.1760G>C (p.Trp587Ser) c.360G>C c.1598G>C (p.Trp533Ser) n.279G>C n.998C>G c.1763G>C (p.Trp588Ser) c.1667G>C (p.Trp556Ser) c.1493G>C (p.Trp498Ser) c.1715G>C (p.Trp572Ser) | ClinVar dbSNP |
| 4 | g.186288496G= | CA1519939820 | F11,F11-AS1 | c.1760G= (p.Trp587=) c.360G= c.1598G= (p.Trp533=) n.279G= n.998C= c.1763G= (p.Trp588=) c.1667G= (p.Trp556=) c.1493G= (p.Trp498=) c.1715G= (p.Trp572=) | dbSNP |