Chr Mutation (hg38) CAid Gene Transcript Linkouts
7g.55191831T>GCA135940EGFRc.2582T>G (p.Leu861Arg)
c.*28+18903T>G (p.=)
c.2447T>G (p.Leu816Arg)
c.2423T>G (p.Leu808Arg)
c.1781T>G (p.Leu594Arg)
ClinVar dbSNP COSMIC
7g.55191831T>ACA176021EGFRc.2582T>A (p.Leu861Gln)
c.*28+18903T>A (p.=)
c.2447T>A (p.Leu816Gln)
c.2423T>A (p.Leu808Gln)
c.1781T>A (p.Leu594Gln)
ClinVar dbSNP COSMIC

Number of alleles fetched