Chr Mutation (hg38) CAid Gene Transcript Linkouts
7g.55174725C>TCA158932443EGFRc.2029C>T (p.Leu677Phe)
c.537C>T
c.2188C>T (p.Leu730Phe)
c.*28+1797C>T (n.*28+1797C>T)
c.2053C>T (p.Leu685Phe)
c.1387C>T (p.Leu463Phe)
dbSNP COSMIC
7g.55174725C>GCA151172EGFRc.2029C>G (p.Leu677Val)
c.537C>G
c.2188C>G (p.Leu730Val)
c.*28+1797C>G (n.*28+1797C>G)
c.2053C>G (p.Leu685Val)
c.1387C>G (p.Leu463Val)
ClinVar dbSNP

Number of alleles fetched