| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 16 | g.31191089G>A | CA257445 | FUS | c.1520G>A (p.Gly507Asp) c.1517G>A (p.Gly506Asp) n.814G>A n.597G>A n.4695G>A c.*693G>A (n.*693G>A) c.1523G>A (p.Gly508Asp) n.411G>A c.1508G>A (p.Gly503Asp) n.1590G>A c.905G>A (p.Gly302Asp) c.1514G>A (p.Gly505Asp) c.1511G>A (p.Gly504Asp) | ClinVar dbSNP |
| 16 | g.31191089G= | CA2216948164 | FUS | c.1520G= (p.Gly507=) c.1517G= (p.Gly506=) n.814G= n.597G= n.4695G= c.*693G= (n.*693G=) c.1523G= (p.Gly508=) n.411G= c.1508G= (p.Gly503=) n.1590G= c.905G= (p.Gly302=) c.1514G= (p.Gly505=) c.1511G= (p.Gly504=) | dbSNP |