Chr Mutation (hg38) CAid Gene Transcript Linkouts
7g.55201204A>GCA4266228EGFRc.2804A>G (p.His935Arg)
c.900-4143A>G
n.707A>G
n.632A>G
c.2963A>G (p.His988Arg)
c.*28+28276A>G (n.*28+28276A>G)
c.2828A>G (p.His943Arg)
c.2162A>G (p.His721Arg)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
7g.55201204A>CCA158465EGFRc.2804A>C (p.His935Pro)
c.900-4143A>C
n.707A>C
n.632A>C
c.2963A>C (p.His988Pro)
c.*28+28276A>C (n.*28+28276A>C)
c.2828A>C (p.His943Pro)
c.2162A>C (p.His721Pro)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
7g.55201204A=CA1708928412EGFRc.2804A= (p.His935=)
c.900-4143A=
n.707A=
n.632A=
c.2963A= (p.His988=)
c.*28+28276A= (n.*28+28276A=)
c.2828A= (p.His943=)
c.2162A= (p.His721=)
dbSNP

Number of alleles fetched