Chr Mutation (hg38) CAid Gene Transcript Linkouts
7g.55181327A>GCA16602544EGFR,EGFR-AS1c.2159A>G (p.His720Arg)
c.667A>G
c.2318A>G (p.His773Arg)
c.*28+8399A>G (n.*28+8399A>G)
c.2183A>G (p.His728Arg)
n.1244T>C
c.1517A>G (p.His506Arg)
ClinVar dbSNP COSMIC
7g.55181327A>TCA367578706EGFR,EGFR-AS1c.2159A>T (p.His720Leu)
c.667A>T
c.2318A>T (p.His773Leu)
c.*28+8399A>T (n.*28+8399A>T)
c.2183A>T (p.His728Leu)
n.1244T>A
c.1517A>T (p.His506Leu)
dbSNP COSMIC
7g.55181327A>CCA367578708EGFR,EGFR-AS1c.2159A>C (p.His720Pro)
c.667A>C
c.2318A>C (p.His773Pro)
c.*28+8399A>C (n.*28+8399A>C)
c.2183A>C (p.His728Pro)
n.1244T>G
c.1517A>C (p.His506Pro)
dbSNP COSMIC

Number of alleles fetched