| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 2 | g.39054637T>A | CA16602968 | SOS1 | n.724A>T n.1535A>T n.462A>T n.704A>T c.797A>T c.697A>T (p.Asn233Tyr) c.790A>T (p.Asn264Tyr) c.676A>T (p.Asn226Tyr) c.673A>T (p.Asn225Tyr) c.526A>T (p.Asn176Tyr) | ClinVar dbSNP COSMIC |
| 2 | g.39054637T= | CA1246153742 | SOS1 | n.724A= n.1535A= n.462A= n.704A= c.797A= c.697A= (p.Asn233=) c.790A= (p.Asn264=) c.676A= (p.Asn226=) c.673A= (p.Asn225=) c.526A= (p.Asn176=) | dbSNP |