Chr Mutation (hg38) CAid Gene Transcript Linkouts
7g.55174773G>ACA16602724EGFRc.2236G>A (p.Glu746Lys)
c.*28+1845G>A (p.=)
c.2101G>A (p.Glu701Lys)
c.2077G>A (p.Glu693Lys)
c.1435G>A (p.Glu479Lys)
ClinVar dbSNP COSMIC
7g.55174773G>CCA180723EGFRc.2236G>C (p.Glu746Gln)
c.*28+1845G>C (p.=)
c.2101G>C (p.Glu701Gln)
c.2077G>C (p.Glu693Gln)
c.1435G>C (p.Glu479Gln)
ClinVar dbSNP

Number of alleles fetched