| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 7 | g.55154028A>C | CA454965697 | EGFR | c.606A>C (p.Arg202=) n.955A>C c.765A>C (p.Arg255=) c.630A>C (p.Arg210=) c.89-1802A>C (n.89-1802A>C) | |
| 7 | g.55154028A>G | CA454965699 | EGFR | c.606A>G (p.Arg202=) n.955A>G c.765A>G (p.Arg255=) c.630A>G (p.Arg210=) c.89-1802A>G (n.89-1802A>G) | |
| 7 | g.55154028A>T | CA454965700 | EGFR | c.606A>T (p.Arg202=) n.955A>T c.765A>T (p.Arg255=) c.630A>T (p.Arg210=) c.89-1802A>T (n.89-1802A>T) | dbSNP |
| 7 | g.55154029G>A | CA367577622 | EGFR | c.607G>A (p.Asp203Asn) n.956G>A c.766G>A (p.Asp256Asn) c.631G>A (p.Asp211Asn) c.89-1801G>A (n.89-1801G>A) | ClinVar dbSNP gnomAD v4 |
| 7 | g.55154029G>C | CA367577621 | EGFR | c.607G>C (p.Asp203His) n.956G>C c.766G>C (p.Asp256His) c.631G>C (p.Asp211His) c.89-1801G>C (n.89-1801G>C) | dbSNP |
| 7 | g.55154029G>T | CA367577620 | EGFR | c.607G>T (p.Asp203Tyr) n.956G>T c.766G>T (p.Asp256Tyr) c.631G>T (p.Asp211Tyr) c.89-1801G>T (n.89-1801G>T) | COSMIC COSMIC |
| 7 | g.55154030A>C | CA367577623 | EGFR | c.608A>C (p.Asp203Ala) n.957A>C c.767A>C (p.Asp256Ala) c.632A>C (p.Asp211Ala) c.89-1800A>C (n.89-1800A>C) | dbSNP COSMIC COSMIC |
| 7 | g.55154030A>G | CA367577624 | EGFR | c.608A>G (p.Asp203Gly) n.957A>G c.767A>G (p.Asp256Gly) c.632A>G (p.Asp211Gly) c.89-1800A>G (n.89-1800A>G) | dbSNP COSMIC COSMIC |
| 7 | g.55154030A>T | CA367577625 | EGFR | c.608A>T (p.Asp203Val) n.957A>T c.767A>T (p.Asp256Val) c.632A>T (p.Asp211Val) c.89-1800A>T (n.89-1800A>T) | dbSNP |
| 7 | g.55154031C>A | CA367577626 | EGFR | c.609C>A (p.Asp203Glu) n.958C>A c.768C>A (p.Asp256Glu) c.633C>A (p.Asp211Glu) c.89-1799C>A (n.89-1799C>A) | |
| 7 | g.55154031C= | CA1708913900 | EGFR | c.609C= (p.Asp203=) n.958C= c.768C= (p.Asp256=) c.633C= (p.Asp211=) c.89-1799C= (n.89-1799C=) | |
| 7 | g.55154031C>G | CA367577627 | EGFR | c.609C>G (p.Asp203Glu) n.958C>G c.768C>G (p.Asp256Glu) c.633C>G (p.Asp211Glu) c.89-1799C>G (n.89-1799C>G) | ClinVar dbSNP |
| 7 | g.55154031C>T | CA4265359 | EGFR | c.609C>T (p.Asp203=) n.958C>T c.768C>T (p.Asp256=) c.633C>T (p.Asp211=) c.89-1799C>T (n.89-1799C>T) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 7 | g.55154032G>A | CA4265360 | EGFR | c.610G>A (p.Glu204Lys) n.959G>A c.769G>A (p.Glu257Lys) c.634G>A (p.Glu212Lys) c.89-1798G>A (n.89-1798G>A) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 7 | g.55154032G>C | CA367577629 | EGFR | c.610G>C (p.Glu204Gln) n.959G>C c.769G>C (p.Glu257Gln) c.634G>C (p.Glu212Gln) c.89-1798G>C (n.89-1798G>C) | |
| 7 | g.55154032G= | CA1708913903 | EGFR | c.610G= (p.Glu204=) n.959G= c.769G= (p.Glu257=) c.634G= (p.Glu212=) c.89-1798G= (n.89-1798G=) | |
| 7 | g.55154032G>T | CA367577628 | EGFR | c.610G>T (p.Glu204Ter) n.959G>T c.769G>T (p.Glu257Ter) c.634G>T (p.Glu212Ter) c.89-1798G>T (n.89-1798G>T) | |
| 7 | g.55154033A>C | CA367577630 | EGFR | c.611A>C (p.Glu204Ala) n.960A>C c.770A>C (p.Glu257Ala) c.635A>C (p.Glu212Ala) c.89-1797A>C (n.89-1797A>C) | |
| 7 | g.55154033A>G | CA367577631 | EGFR | c.611A>G (p.Glu204Gly) n.960A>G c.770A>G (p.Glu257Gly) c.635A>G (p.Glu212Gly) c.89-1797A>G (n.89-1797A>G) | gnomAD v4 |
| 7 | g.55154033A>T | CA367577632 | EGFR | c.611A>T (p.Glu204Val) n.960A>T c.770A>T (p.Glu257Val) c.635A>T (p.Glu212Val) c.89-1797A>T (n.89-1797A>T) | |
| 7 | g.55154033_55154034insCTCC | CA2714951057 | EGFR | c.611_612insCTCC (p.Glu204AspfsTer?) n.960_961insCTCC c.770_771insCTCC (p.Glu257AspfsTer?) c.635_636insCTCC (p.Glu212AspfsTer?) c.89-1797_89-1796insCTCC (n.89-1797_89-1796insCTCC) | dbSNP |
| 7 | g.55154034A>C | CA367577633 | EGFR | c.612A>C (p.Glu204Asp) n.961A>C c.771A>C (p.Glu257Asp) c.636A>C (p.Glu212Asp) c.89-1796A>C (n.89-1796A>C) | dbSNP |
| 7 | g.55154034A>G | CA454965703 | EGFR | c.612A>G (p.Glu204=) n.961A>G c.771A>G (p.Glu257=) c.636A>G (p.Glu212=) c.89-1796A>G (n.89-1796A>G) | dbSNP |
| 7 | g.55154034A>T | CA367577634 | EGFR | c.612A>T (p.Glu204Asp) n.961A>T c.771A>T (p.Glu257Asp) c.636A>T (p.Glu212Asp) c.89-1796A>T (n.89-1796A>T) | dbSNP |
| 7 | g.55154035G>A | CA367577635 | EGFR | c.613G>A (p.Ala205Thr) n.962G>A c.772G>A (p.Ala258Thr) c.637G>A (p.Ala213Thr) c.89-1795G>A (n.89-1795G>A) | |
| 7 | g.55154035G>C | CA367577636 | EGFR | c.613G>C (p.Ala205Pro) n.962G>C c.772G>C (p.Ala258Pro) c.637G>C (p.Ala213Pro) c.89-1795G>C (n.89-1795G>C) | |
| 7 | g.55154035G>T | CA367577637 | EGFR | c.613G>T (p.Ala205Ser) n.962G>T c.772G>T (p.Ala258Ser) c.637G>T (p.Ala213Ser) c.89-1795G>T (n.89-1795G>T) | gnomAD v4 |
| 7 | g.55154036C>A | CA367577638 | EGFR | c.614C>A (p.Ala205Asp) n.963C>A c.773C>A (p.Ala258Asp) c.638C>A (p.Ala213Asp) c.89-1794C>A (n.89-1794C>A) | dbSNP |
| 7 | g.55154036C>G | CA367577639 | EGFR | c.614C>G (p.Ala205Gly) n.963C>G c.773C>G (p.Ala258Gly) c.638C>G (p.Ala213Gly) c.89-1794C>G (n.89-1794C>G) | dbSNP |
| 7 | g.55154036C>T | CA367577640 | EGFR | c.614C>T (p.Ala205Val) n.963C>T c.773C>T (p.Ala258Val) c.638C>T (p.Ala213Val) c.89-1794C>T (n.89-1794C>T) | dbSNP |
| 7 | g.55154037C>A | CA454965707 | EGFR | c.615C>A (p.Ala205=) n.964C>A c.774C>A (p.Ala258=) c.639C>A (p.Ala213=) c.89-1793C>A (n.89-1793C>A) | dbSNP |
| 7 | g.55154037C= | CA1708913905 | EGFR | c.615C= (p.Ala205=) n.964C= c.774C= (p.Ala258=) c.639C= (p.Ala213=) c.89-1793C= (n.89-1793C=) | |
| 7 | g.55154037C>G | CA454965708 | EGFR | c.615C>G (p.Ala205=) n.964C>G c.774C>G (p.Ala258=) c.639C>G (p.Ala213=) c.89-1793C>G (n.89-1793C>G) | dbSNP |
| 7 | g.55154037C>T | CA4265361 | EGFR | c.615C>T (p.Ala205=) n.964C>T c.774C>T (p.Ala258=) c.639C>T (p.Ala213=) c.89-1793C>T (n.89-1793C>T) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 7 | g.55154038A= | CA1708913907 | EGFR | c.616A= (p.Thr206=) n.965A= c.775A= (p.Thr259=) c.640A= (p.Thr214=) c.89-1792A= (n.89-1792A=) | |
| 7 | g.55154038A>C | CA367577643 | EGFR | c.616A>C (p.Thr206Pro) n.965A>C c.775A>C (p.Thr259Pro) c.640A>C (p.Thr214Pro) c.89-1792A>C (n.89-1792A>C) | dbSNP gnomAD v2 gnomAD v4 |
| 7 | g.55154038A>G | CA367577641 | EGFR | c.616A>G (p.Thr206Ala) n.965A>G c.775A>G (p.Thr259Ala) c.640A>G (p.Thr214Ala) c.89-1792A>G (n.89-1792A>G) | ClinVar dbSNP gnomAD v4 |
| 7 | g.55154038A>T | CA367577642 | EGFR | c.616A>T (p.Thr206Ser) n.965A>T c.775A>T (p.Thr259Ser) c.640A>T (p.Thr214Ser) c.89-1792A>T (n.89-1792A>T) | dbSNP |
| 7 | g.55154039C>A | CA367577644 | EGFR | c.617C>A (p.Thr206Lys) n.966C>A c.776C>A (p.Thr259Lys) c.641C>A (p.Thr214Lys) c.89-1791C>A (n.89-1791C>A) | ClinVar dbSNP |
| 7 | g.55154039C= | CA1708913914 | EGFR | c.617C= (p.Thr206=) n.966C= c.776C= (p.Thr259=) c.641C= (p.Thr214=) c.89-1791C= (n.89-1791C=) | |
| 7 | g.55154039C>G | CA367577645 | EGFR | c.617C>G (p.Thr206Arg) n.966C>G c.776C>G (p.Thr259Arg) c.641C>G (p.Thr214Arg) c.89-1791C>G (n.89-1791C>G) | dbSNP |
| 7 | g.55154039C>T | CA4265362 | EGFR | c.617C>T (p.Thr206Met) n.966C>T c.776C>T (p.Thr259Met) c.641C>T (p.Thr214Met) c.89-1791C>T (n.89-1791C>T) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 7 | g.55154040G>A | CA4265363 | EGFR | c.618G>A (p.Thr206=) n.967G>A c.777G>A (p.Thr259=) c.642G>A (p.Thr214=) c.89-1790G>A (n.89-1790G>A) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC |
| 7 | g.55154040G>C | CA454965712 | EGFR | c.618G>C (p.Thr206=) n.967G>C c.777G>C (p.Thr259=) c.642G>C (p.Thr214=) c.89-1790G>C (n.89-1790G>C) | dbSNP |
| 7 | g.55154040G= | CA1708913922 | EGFR | c.618G= (p.Thr206=) n.967G= c.777G= (p.Thr259=) c.642G= (p.Thr214=) c.89-1790G= (n.89-1790G=) | |
| 7 | g.55154040G>T | CA158912164 | EGFR | c.618G>T (p.Thr206=) n.967G>T c.777G>T (p.Thr259=) c.642G>T (p.Thr214=) c.89-1790G>T (n.89-1790G>T) | ClinVar dbSNP gnomAD v4 |
| 7 | g.55154041T>A | CA367577646 | EGFR | c.619T>A (p.Cys207Ser) n.968T>A c.778T>A (p.Cys260Ser) c.643T>A (p.Cys215Ser) c.89-1789T>A (n.89-1789T>A) | dbSNP |
| 7 | g.55154041T>C | CA367577647 | EGFR | c.619T>C (p.Cys207Arg) n.968T>C c.778T>C (p.Cys260Arg) c.643T>C (p.Cys215Arg) c.89-1789T>C (n.89-1789T>C) | dbSNP |
| 7 | g.55154041T>G | CA367577648 | EGFR | c.619T>G (p.Cys207Gly) n.968T>G c.778T>G (p.Cys260Gly) c.643T>G (p.Cys215Gly) c.89-1789T>G (n.89-1789T>G) | dbSNP |
| 7 | g.55154042G>A | CA367577649 | EGFR | c.620G>A (p.Cys207Tyr) n.969G>A c.779G>A (p.Cys260Tyr) c.644G>A (p.Cys215Tyr) c.89-1788G>A (n.89-1788G>A) | dbSNP |