Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
7 | g.55181378C>T | CA090928 | EGFR,EGFR-AS1 | c.2210C>T (p.Thr737Met) c.718C>T c.2369C>T (p.Thr790Met) c.*28+8450C>T (n.*28+8450C>T) c.2234C>T (p.Thr745Met) n.1193G>A c.1568C>T (p.Thr523Met) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
7 | g.55181378C= | CA1708905489 | EGFR,EGFR-AS1 | c.2210C= (p.Thr737=) c.718C= c.2369C= (p.Thr790=) c.*28+8450C= (n.*28+8450C=) c.2234C= (p.Thr745=) n.1193G= c.1568C= (p.Thr523=) | dbSNP |
7 | g.55181378C>A | CA367578852 | EGFR,EGFR-AS1 | c.2210C>A (p.Thr737Lys) c.718C>A c.2369C>A (p.Thr790Lys) c.*28+8450C>A (n.*28+8450C>A) c.2234C>A (p.Thr745Lys) n.1193G>T c.1568C>A (p.Thr523Lys) | dbSNP gnomAD v4 |