Chr Mutation (hg38) CAid Gene Transcript Linkouts
7g.55174014G>ACA126722EGFRc.1996G>A (p.Gly666Ser)
c.504G>A
c.2155G>A (p.Gly719Ser)
c.*28+1086G>A (n.*28+1086G>A)
c.2020G>A (p.Gly674Ser)
c.1354G>A (p.Gly452Ser)
ClinVar dbSNP COSMIC
7g.55174014G>CCA135772EGFRc.1996G>C (p.Gly666Arg)
c.504G>C
c.2155G>C (p.Gly719Arg)
c.*28+1086G>C (n.*28+1086G>C)
c.2020G>C (p.Gly674Arg)
c.1354G>C (p.Gly452Arg)
ClinVar dbSNP
7g.55174014G>TCA126719EGFRc.1996G>T (p.Gly666Cys)
c.504G>T
c.2155G>T (p.Gly719Cys)
c.*28+1086G>T (n.*28+1086G>T)
c.2020G>T (p.Gly674Cys)
c.1354G>T (p.Gly452Cys)
ClinVar dbSNP COSMIC

Number of alleles fetched