| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 2 | g.39058696C>T | CA261739 | SOS1 | n.349G>A n.1160G>A n.87G>A n.329G>A c.422G>A c.322G>A (p.Glu108Lys) c.151G>A (p.Glu51Lys) c.415G>A (p.Glu139Lys) c.301G>A (p.Glu101Lys) c.298G>A (p.Glu100Lys) | ClinVar dbSNP COSMIC |
| 2 | g.39058696C= | CA1246156073 | SOS1 | n.349G= n.1160G= n.87G= n.329G= c.422G= c.322G= (p.Glu108=) c.151G= (p.Glu51=) c.415G= (p.Glu139=) c.301G= (p.Glu101=) c.298G= (p.Glu100=) | dbSNP |