Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
8 | g.38417333T>C | CA16602864 | FGFR1 | c.1636A>G (p.Asn546Asp) c.1624A>G (p.Asn542Asp) n.2529A>G n.402A>G c.1816A>G (p.Asn606Asp) n.2324A>G c.1357A>G (p.Asn453Asp) c.*1282A>G (n.*1282A>G) c.*1603A>G (n.*1603A>G) n.3130A>G c.1363A>G (p.Asn455Asp) c.1606A>G (p.Asn536Asp) c.*686A>G (n.*686A>G) c.1369A>G (p.Asn457Asp) c.1630A>G (p.Asn544Asp) c.1729A>G (p.Asn577Asp) n.803A>G c.1513A>G (n.1513A>G) n.3915A>G n.1158A>G n.182A>G c.*531A>G (n.*531A>G) c.1612A>G (p.Asn538Asp) c.1735A>G (p.Asn579Asp) c.1468A>G (p.Asn490Asp) c.1462A>G (p.Asn488Asp) c.1345A>G (p.Asn449Asp) c.1723A>G (p.Asn575Asp) c.1456A>G (p.Asn486Asp) c.664A>G (p.Asn222Asp) n.1884A>G | ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC COSMIC |
8 | g.38417333T= | CA1777536243 | FGFR1 | c.1636A= (p.Asn546=) c.1624A= (p.Asn542=) n.2529A= n.402A= c.1816A= (p.Asn606=) n.2324A= c.1357A= (p.Asn453=) c.*1282A= (n.*1282A=) c.*1603A= (n.*1603A=) n.3130A= c.1363A= (p.Asn455=) c.1606A= (p.Asn536=) c.*686A= (n.*686A=) c.1369A= (p.Asn457=) c.1630A= (p.Asn544=) c.1729A= (p.Asn577=) n.803A= c.1513A= (n.1513A=) n.3915A= n.1158A= n.182A= c.*531A= (n.*531A=) c.1612A= (p.Asn538=) c.1735A= (p.Asn579=) c.1468A= (p.Asn490=) c.1462A= (p.Asn488=) c.1345A= (p.Asn449=) c.1723A= (p.Asn575=) c.1456A= (p.Asn486=) c.664A= (p.Asn222=) n.1884A= | dbSNP |