Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
7 | g.55200351C>T | CA4266199 | EGFR | c.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 |
7 | g.55200351C>G | CA4266201 | EGFR | c.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 |
7 | g.55200351C>A | CA4266200 | EGFR | c.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 |