Chr Mutation (hg38) CAid Gene Transcript Linkouts
7g.55200351C>TCA4266199EGFRc.2725C>T (p.Arg909Cys)
c.900-4996C>T
n.628C>T
c.2884C>T (p.Arg962Cys)
c.*28+27423C>T (n.*28+27423C>T)
c.2749C>T (p.Arg917Cys)
n.214C>T
c.2083C>T (p.Arg695Cys)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
7g.55200351C>GCA4266201EGFRc.2725C>G (p.Arg909Gly)
c.900-4996C>G
n.628C>G
c.2884C>G (p.Arg962Gly)
c.*28+27423C>G (n.*28+27423C>G)
c.2749C>G (p.Arg917Gly)
n.214C>G
c.2083C>G (p.Arg695Gly)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
7g.55200351C>ACA4266200EGFRc.2725C>A (p.Arg909Ser)
c.900-4996C>A
n.628C>A
c.2884C>A (p.Arg962Ser)
c.*28+27423C>A (n.*28+27423C>A)
c.2749C>A (p.Arg917Ser)
n.214C>A
c.2083C>A (p.Arg695Ser)
dbSNP ExAC gnomAD v2 gnomAD v4

Number of alleles fetched