Chr Mutation (hg38) CAid Gene Transcript Linkouts
7g.55201223C>TCA4266232EGFRc.2823C>T (p.Asp941=)
c.900-4124C>T
n.726C>T
n.651C>T
c.2982C>T (p.Asp994=)
c.*28+28295C>T (n.*28+28295C>T)
c.2847C>T (p.Asp949=)
c.2181C>T (p.Asp727=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
7g.55201223C>GCA367582409EGFRc.2823C>G (p.Asp941Glu)
c.900-4124C>G
n.726C>G
n.651C>G
c.2982C>G (p.Asp994Glu)
c.*28+28295C>G (n.*28+28295C>G)
c.2847C>G (p.Asp949Glu)
c.2181C>G (p.Asp727Glu)
dbSNP
7g.55201223C=CA1708928419EGFRc.2823C= (p.Asp941=)
c.900-4124C=
n.726C=
n.651C=
c.2982C= (p.Asp994=)
c.*28+28295C= (n.*28+28295C=)
c.2847C= (p.Asp949=)
c.2181C= (p.Asp727=)
dbSNP
7g.55201223C>ACA367582410EGFRc.2823C>A (p.Asp941Glu)
c.900-4124C>A
n.726C>A
n.651C>A
c.2982C>A (p.Asp994Glu)
c.*28+28295C>A (n.*28+28295C>A)
c.2847C>A (p.Asp949Glu)
c.2181C>A (p.Asp727Glu)
dbSNP

Number of alleles fetched