Chr Mutation (hg38) CAid Gene Transcript Linkouts
7g.55174015G>CCA135775EGFRc.1997G>C (p.Gly666Ala)
c.505G>C
c.2156G>C (p.Gly719Ala)
c.*28+1087G>C (n.*28+1087G>C)
c.2021G>C (p.Gly674Ala)
c.1355G>C (p.Gly452Ala)
ClinVar dbSNP COSMIC
7g.55174015G>ACA16602537EGFRc.1997G>A (p.Gly666Asp)
c.505G>A
c.2156G>A (p.Gly719Asp)
c.*28+1087G>A (n.*28+1087G>A)
c.2021G>A (p.Gly674Asp)
c.1355G>A (p.Gly452Asp)
ClinVar dbSNP COSMIC

Number of alleles fetched