| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 4 | g.54728096T>A | CA16602404 | KIT | c.1956T>A (p.Asn652Lys) n.2043T>A c.1953T>A (p.Asn651Lys) c.1968T>A (p.Asn656Lys) n.2380T>A n.2123T>A c.1455T>A (p.Asn485Lys) n.2183T>A n.875T>A c.1965T>A (p.Asn655Lys) n.2062T>A | ClinVar dbSNP COSMIC |
| 4 | g.54728096T>G | CA16602405 | KIT | c.1956T>G (p.Asn652Lys) n.2043T>G c.1953T>G (p.Asn651Lys) c.1968T>G (p.Asn656Lys) n.2380T>G n.2123T>G c.1455T>G (p.Asn485Lys) n.2183T>G n.875T>G c.1965T>G (p.Asn655Lys) n.2062T>G | ClinVar dbSNP COSMIC |
| 4 | g.54728096T>C | CA439291516 | KIT | c.1956T>C (p.Asn652=) n.2043T>C c.1953T>C (p.Asn651=) c.1968T>C (p.Asn656=) n.2380T>C n.2123T>C c.1455T>C (p.Asn485=) n.2183T>C n.875T>C c.1965T>C (p.Asn655=) n.2062T>C | dbSNP |