Chr Mutation (hg38) CAid Gene Transcript Linkouts
7g.55181437G>CCA367578983EGFR,EGFR-AS1c.2269G>C (p.Gly757Arg)
c.777G>C
c.2428G>C (p.Gly810Arg)
c.*28+8509G>C (n.*28+8509G>C)
c.2293G>C (p.Gly765Arg)
n.1134C>G
c.1627G>C (p.Gly543Arg)
dbSNP
7g.55181437G>TCA367578982EGFR,EGFR-AS1c.2269G>T (p.Gly757Cys)
c.777G>T
c.2428G>T (p.Gly810Cys)
c.*28+8509G>T (n.*28+8509G>T)
c.2293G>T (p.Gly765Cys)
n.1134C>A
c.1627G>T (p.Gly543Cys)
dbSNP
7g.55181437G>ACA16602726EGFR,EGFR-AS1c.2269G>A (p.Gly757Ser)
c.777G>A
c.2428G>A (p.Gly810Ser)
c.*28+8509G>A (n.*28+8509G>A)
c.2293G>A (p.Gly765Ser)
n.1134C>T
c.1627G>A (p.Gly543Ser)
ClinVar dbSNP COSMIC
7g.55181437G=CA1708905683EGFR,EGFR-AS1c.2269G= (p.Gly757=)
c.777G=
c.2428G= (p.Gly810=)
c.*28+8509G= (n.*28+8509G=)
c.2293G= (p.Gly765=)
n.1134C=
c.1627G= (p.Gly543=)
dbSNP

Number of alleles fetched