| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 16 | g.31185031G>A | CA259634 | FUS | c.616G>A (p.Gly206Ser) c.613G>A (p.Gly205Ser) n.681G>A c.604G>A (p.Gly202Ser) n.721G>A c.36G>A (p.Ala12=) c.610G>A (p.Gly204Ser) c.607G>A (p.Gly203Ser) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 16 | g.31185031G= | CA2216944798 | FUS | c.616G= (p.Gly206=) c.613G= (p.Gly205=) n.681G= c.604G= (p.Gly202=) n.721G= c.36G= (p.Ala12=) c.610G= (p.Gly204=) c.607G= (p.Gly203=) | dbSNP |