Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
7 | g.55201204A>G | CA4266228 | EGFR | c.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 |
7 | g.55201204A>C | CA158465 | EGFR | c.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 |
7 | g.55201204A= | CA1708928412 | EGFR | c.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 |