UPDATE - Protein Allele ID & Protein Sequence HGVS Requests Partially Restored
Protein allele requests are no longer disabled.
Currently, hypothetical explanatory transcript generation is not part of the response and is being investigated.
Protein allele requests are no longer disabled.
Currently, hypothetical explanatory transcript generation is not part of the response and is being investigated.
| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 7 | g.55191747_55191835delinsTGGTGCACCGCGACCTGGCAGCCAGGAACGTACTGGTGAAAACACCGCAGCATGTCAAGATCACAGATTTTGGGCTGGCCAAACTGCTG | CA1708922454 | EGFR | c.2339_2427delinsTGGTGCACCGCGACCTGGCAGCCAGGAACGTACTGGTGAAAACACCGCAGCATGTCAAGATCACAGATTTTGGGCTGGCCAAACTGCTG (p.Leu780=) c.847_899+36delinsTGGTGCACCGCGACCTGGCAGCCAGGAACGTACTGGTGAAAACACCGCAGCATGTCAAGATCACAGATTTTGGGCTGGCCAAACTGCTG c.2498_2586delinsTGGTGCACCGCGACCTGGCAGCCAGGAACGTACTGGTGAAAACACCGCAGCATGTCAAGATCACAGATTTTGGGCTGGCCAAACTGCTG (p.Leu833=) c.*28+18819_*28+18907delinsTGGTGCACCGCGACCTGGCAGCCAGGAACGTACTGGTGAAAACACCGCAGCATGTCAAGATCACAGATTTTGGGCTGGCCAAACTGCTG (n.*28+18819_*28+18907delinsTGGTGCACCGCGACCTGGCAGCCAGGAACGTACTGGTGAAAACACCGCAGCATGTCAAGATCACAGATTTTGGGCTGGCCAAACTGCTG) c.2363_2451delinsTGGTGCACCGCGACCTGGCAGCCAGGAACGTACTGGTGAAAACACCGCAGCATGTCAAGATCACAGATTTTGGGCTGGCCAAACTGCTG (p.Leu788=) c.1697_1785delinsTGGTGCACCGCGACCTGGCAGCCAGGAACGTACTGGTGAAAACACCGCAGCATGTCAAGATCACAGATTTTGGGCTGGCCAAACTGCTG (p.Leu566=) | |
| 7 | g.55191753_55191840del | CA176020 | EGFR | c.2345_2432del (p.His782ArgfsTer?) c.853_899+41del c.2504_2591del (p.His835ArgfsTer?) c.*28+18825_*28+18912del (n.*28+18825_*28+18912del) c.2369_2456del (p.His790ArgfsTer?) c.1703_1790del (p.His568ArgfsTer?) | ClinVar dbSNP |
| 7 | g.55191770A>C | CA454965611 | EGFR | c.2362A>C (p.Arg788=) c.870A>C c.2521A>C (p.Arg841=) c.*28+18842A>C (n.*28+18842A>C) c.2386A>C (p.Arg796=) c.1720A>C (p.Arg574=) | |
| 7 | g.55191770A>G | CA367580163 | EGFR | c.2362A>G (p.Arg788Gly) c.870A>G c.2521A>G (p.Arg841Gly) c.*28+18842A>G (n.*28+18842A>G) c.2386A>G (p.Arg796Gly) c.1720A>G (p.Arg574Gly) | |
| 7 | g.55191770A>T | CA367580164 | EGFR | c.2362A>T (p.Arg788Trp) c.870A>T c.2521A>T (p.Arg841Trp) c.*28+18842A>T (n.*28+18842A>T) c.2386A>T (p.Arg796Trp) c.1720A>T (p.Arg574Trp) | dbSNP |
| 7 | g.55191771G>A | CA367580165 | EGFR | c.2363G>A (p.Arg788Lys) c.871G>A c.2522G>A (p.Arg841Lys) c.*28+18843G>A (n.*28+18843G>A) c.2387G>A (p.Arg796Lys) c.1721G>A (p.Arg574Lys) | COSMIC |
| 7 | g.55191771G>C | CA367580166 | EGFR | c.2363G>C (p.Arg788Thr) c.871G>C c.2522G>C (p.Arg841Thr) c.*28+18843G>C (n.*28+18843G>C) c.2387G>C (p.Arg796Thr) c.1721G>C (p.Arg574Thr) | |
| 7 | g.55191771G>T | CA367580167 | EGFR | c.2363G>T (p.Arg788Met) c.871G>T c.2522G>T (p.Arg841Met) c.*28+18843G>T (n.*28+18843G>T) c.2387G>T (p.Arg796Met) c.1721G>T (p.Arg574Met) | |
| 7 | g.55191772G>A | CA454965612 | EGFR | c.2364G>A (p.Arg788=) c.872G>A c.2523G>A (p.Arg841=) c.*28+18844G>A (n.*28+18844G>A) c.2388G>A (p.Arg796=) c.1722G>A (p.Arg574=) | ClinVar dbSNP gnomAD v4 COSMIC |
| 7 | g.55191772G>C | CA4266112 | EGFR | c.2364G>C (p.Arg788Ser) c.872G>C c.2523G>C (p.Arg841Ser) c.*28+18844G>C (n.*28+18844G>C) c.2388G>C (p.Arg796Ser) c.1722G>C (p.Arg574Ser) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 7 | g.55191772G= | CA1708922531 | EGFR | c.2364G= (p.Arg788=) c.872G= c.2523G= (p.Arg841=) c.*28+18844G= (n.*28+18844G=) c.2388G= (p.Arg796=) c.1722G= (p.Arg574=) | |
| 7 | g.55191772G>T | CA367580168 | EGFR | c.2364G>T (p.Arg788Ser) c.872G>T c.2523G>T (p.Arg841Ser) c.*28+18844G>T (n.*28+18844G>T) c.2388G>T (p.Arg796Ser) c.1722G>T (p.Arg574Ser) | dbSNP |
| 7 | g.55191773A= | CA1708922535 | EGFR | c.2365A= (p.Asn789=) c.873A= c.2524A= (p.Asn842=) c.*28+18845A= (n.*28+18845A=) c.2389A= (p.Asn797=) c.1723A= (p.Asn575=) | |
| 7 | g.55191773A>C | CA367580169 | EGFR | c.2365A>C (p.Asn789His) c.873A>C c.2524A>C (p.Asn842His) c.*28+18845A>C (n.*28+18845A>C) c.2389A>C (p.Asn797His) c.1723A>C (p.Asn575His) | dbSNP COSMIC |
| 7 | g.55191773A>G | CA158934194 | EGFR | c.2365A>G (p.Asn789Asp) c.873A>G c.2524A>G (p.Asn842Asp) c.*28+18845A>G (n.*28+18845A>G) c.2389A>G (p.Asn797Asp) c.1723A>G (p.Asn575Asp) | ClinVar dbSNP COSMIC |
| 7 | g.55191773A>T | CA367580170 | EGFR | c.2365A>T (p.Asn789Tyr) c.873A>T c.2524A>T (p.Asn842Tyr) c.*28+18845A>T (n.*28+18845A>T) c.2389A>T (p.Asn797Tyr) c.1723A>T (p.Asn575Tyr) | dbSNP |
| 7 | g.55191774A>C | CA367580171 | EGFR | c.2366A>C (p.Asn789Thr) c.874A>C c.2525A>C (p.Asn842Thr) c.*28+18846A>C (n.*28+18846A>C) c.2390A>C (p.Asn797Thr) c.1724A>C (p.Asn575Thr) | dbSNP |
| 7 | g.55191774A>G | CA367580172 | EGFR | c.2366A>G (p.Asn789Ser) c.874A>G c.2525A>G (p.Asn842Ser) c.*28+18846A>G (n.*28+18846A>G) c.2390A>G (p.Asn797Ser) c.1724A>G (p.Asn575Ser) | dbSNP |
| 7 | g.55191774A>T | CA367580173 | EGFR | c.2366A>T (p.Asn789Ile) c.874A>T c.2525A>T (p.Asn842Ile) c.*28+18846A>T (n.*28+18846A>T) c.2390A>T (p.Asn797Ile) c.1724A>T (p.Asn575Ile) | dbSNP |
| 7 | g.55191775C>A | CA367580174 | EGFR | c.2367C>A (p.Asn789Lys) c.875C>A c.2526C>A (p.Asn842Lys) c.*28+18847C>A (n.*28+18847C>A) c.2391C>A (p.Asn797Lys) c.1725C>A (p.Asn575Lys) | dbSNP |
| 7 | g.55191775C= | CA1708922541 | EGFR | c.2367C= (p.Asn789=) c.875C= c.2526C= (p.Asn842=) c.*28+18847C= (n.*28+18847C=) c.2391C= (p.Asn797=) c.1725C= (p.Asn575=) | |
| 7 | g.55191775C>G | CA367580175 | EGFR | c.2367C>G (p.Asn789Lys) c.875C>G c.2526C>G (p.Asn842Lys) c.*28+18847C>G (n.*28+18847C>G) c.2391C>G (p.Asn797Lys) c.1725C>G (p.Asn575Lys) | dbSNP |
| 7 | g.55191775C>T | CA454965615 | EGFR | c.2367C>T (p.Asn789=) c.875C>T c.2526C>T (p.Asn842=) c.*28+18847C>T (n.*28+18847C>T) c.2391C>T (p.Asn797=) c.1725C>T (p.Asn575=) | ClinVar dbSNP gnomAD v4 COSMIC |
| 7 | g.55191776G>A | CA16602666 | EGFR | c.2368G>A (p.Val790Ile) c.876G>A c.2527G>A (p.Val843Ile) c.*28+18848G>A (n.*28+18848G>A) c.2392G>A (p.Val798Ile) c.1726G>A (p.Val576Ile) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 7 | g.55191776G>C | CA367580176 | EGFR | c.2368G>C (p.Val790Leu) c.876G>C c.2527G>C (p.Val843Leu) c.*28+18848G>C (n.*28+18848G>C) c.2392G>C (p.Val798Leu) c.1726G>C (p.Val576Leu) | dbSNP gnomAD v4 COSMIC |
| 7 | g.55191776G= | CA1708922547 | EGFR | c.2368G= (p.Val790=) c.876G= c.2527G= (p.Val843=) c.*28+18848G= (n.*28+18848G=) c.2392G= (p.Val798=) c.1726G= (p.Val576=) | |
| 7 | g.55191776G>T | CA367580177 | EGFR | c.2368G>T (p.Val790Leu) c.876G>T c.2527G>T (p.Val843Leu) c.*28+18848G>T (n.*28+18848G>T) c.2392G>T (p.Val798Leu) c.1726G>T (p.Val576Leu) | COSMIC |
| 7 | g.55191777T>A | CA367580178 | EGFR | c.2369T>A (p.Val790Glu) c.877T>A c.2528T>A (p.Val843Glu) c.*28+18849T>A (n.*28+18849T>A) c.2393T>A (p.Val798Glu) c.1727T>A (p.Val576Glu) | dbSNP |
| 7 | g.55191777T>C | CA367580179 | EGFR | c.2369T>C (p.Val790Ala) c.877T>C c.2528T>C (p.Val843Ala) c.*28+18849T>C (n.*28+18849T>C) c.2393T>C (p.Val798Ala) c.1727T>C (p.Val576Ala) | dbSNP |
| 7 | g.55191777T>G | CA367580180 | EGFR | c.2369T>G (p.Val790Gly) c.877T>G c.2528T>G (p.Val843Gly) c.*28+18849T>G (n.*28+18849T>G) c.2393T>G (p.Val798Gly) c.1727T>G (p.Val576Gly) | dbSNP |
| 7 | g.55191778A>C | CA454965616 | EGFR | c.2370A>C (p.Val790=) c.878A>C c.2529A>C (p.Val843=) c.*28+18850A>C (n.*28+18850A>C) c.2394A>C (p.Val798=) c.1728A>C (p.Val576=) | dbSNP |
| 7 | g.55191778A>G | CA454965617 | EGFR | c.2370A>G (p.Val790=) c.878A>G c.2529A>G (p.Val843=) c.*28+18850A>G (n.*28+18850A>G) c.2394A>G (p.Val798=) c.1728A>G (p.Val576=) | ClinVar |
| 7 | g.55191778A>T | CA454965618 | EGFR | c.2370A>T (p.Val790=) c.878A>T c.2529A>T (p.Val843=) c.*28+18850A>T (n.*28+18850A>T) c.2394A>T (p.Val798=) c.1728A>T (p.Val576=) | dbSNP |
| 7 | g.55191779C>A | CA367580181 | EGFR | c.2371C>A (p.Leu791Met) c.879C>A c.2530C>A (p.Leu844Met) c.*28+18851C>A (n.*28+18851C>A) c.2395C>A (p.Leu799Met) c.1729C>A (p.Leu577Met) | dbSNP |
| 7 | g.55191779C>G | CA367580182 | EGFR | c.2371C>G (p.Leu791Val) c.879C>G c.2530C>G (p.Leu844Val) c.*28+18851C>G (n.*28+18851C>G) c.2395C>G (p.Leu799Val) c.1729C>G (p.Leu577Val) | dbSNP COSMIC |
| 7 | g.55191779C>T | CA454965619 | EGFR | c.2371C>T (p.Leu791=) c.879C>T c.2530C>T (p.Leu844=) c.*28+18851C>T (n.*28+18851C>T) c.2395C>T (p.Leu799=) c.1729C>T (p.Leu577=) | dbSNP |
| 7 | g.55191780T>A | CA367580183 | EGFR | c.2372T>A (p.Leu791Gln) c.880T>A c.2531T>A (p.Leu844Gln) c.*28+18852T>A (n.*28+18852T>A) c.2396T>A (p.Leu799Gln) c.1730T>A (p.Leu577Gln) | |
| 7 | g.55191780T>C | CA367580184 | EGFR | c.2372T>C (p.Leu791Pro) c.880T>C c.2531T>C (p.Leu844Pro) c.*28+18852T>C (n.*28+18852T>C) c.2396T>C (p.Leu799Pro) c.1730T>C (p.Leu577Pro) | COSMIC |
| 7 | g.55191780T>G | CA367580185 | EGFR | c.2372T>G (p.Leu791Arg) c.880T>G c.2531T>G (p.Leu844Arg) c.*28+18852T>G (n.*28+18852T>G) c.2396T>G (p.Leu799Arg) c.1730T>G (p.Leu577Arg) | |
| 7 | g.55191781G>A | CA454965620 | EGFR | c.2373G>A (p.Leu791=) c.881G>A c.2532G>A (p.Leu844=) c.*28+18853G>A (n.*28+18853G>A) c.2397G>A (p.Leu799=) c.1731G>A (p.Leu577=) | dbSNP gnomAD v4 |
| 7 | g.55191781G>C | CA454965621 | EGFR | c.2373G>C (p.Leu791=) c.881G>C c.2532G>C (p.Leu844=) c.*28+18853G>C (n.*28+18853G>C) c.2397G>C (p.Leu799=) c.1731G>C (p.Leu577=) | dbSNP |
| 7 | g.55191781G>T | CA454965622 | EGFR | c.2373G>T (p.Leu791=) c.881G>T c.2532G>T (p.Leu844=) c.*28+18853G>T (n.*28+18853G>T) c.2397G>T (p.Leu799=) c.1731G>T (p.Leu577=) | dbSNP |
| 7 | g.55191782G>A | CA367580186 | EGFR | c.2374G>A (p.Val792Met) c.882G>A c.2533G>A (p.Val845Met) c.*28+18854G>A (n.*28+18854G>A) c.2398G>A (p.Val800Met) c.1732G>A (p.Val578Met) | ClinVar dbSNP COSMIC |
| 7 | g.55191782G>C | CA367580187 | EGFR | c.2374G>C (p.Val792Leu) c.882G>C c.2533G>C (p.Val845Leu) c.*28+18854G>C (n.*28+18854G>C) c.2398G>C (p.Val800Leu) c.1732G>C (p.Val578Leu) | ClinVar dbSNP |
| 7 | g.55191782G= | CA1708922554 | EGFR | c.2374G= (p.Val792=) c.882G= c.2533G= (p.Val845=) c.*28+18854G= (n.*28+18854G=) c.2398G= (p.Val800=) c.1732G= (p.Val578=) | |
| 7 | g.55191782G>T | CA367580188 | EGFR | c.2374G>T (p.Val792Leu) c.882G>T c.2533G>T (p.Val845Leu) c.*28+18854G>T (n.*28+18854G>T) c.2398G>T (p.Val800Leu) c.1732G>T (p.Val578Leu) | dbSNP |
| 7 | g.55191783T>A | CA367580189 | EGFR | c.2375T>A (p.Val792Glu) c.883T>A c.2534T>A (p.Val845Glu) c.*28+18855T>A (n.*28+18855T>A) c.2399T>A (p.Val800Glu) c.1733T>A (p.Val578Glu) | |
| 7 | g.55191783T>C | CA367580190 | EGFR | c.2375T>C (p.Val792Ala) c.883T>C c.2534T>C (p.Val845Ala) c.*28+18855T>C (n.*28+18855T>C) c.2399T>C (p.Val800Ala) c.1733T>C (p.Val578Ala) | COSMIC |
| 7 | g.55191783T>G | CA367580191 | EGFR | c.2375T>G (p.Val792Gly) c.883T>G c.2534T>G (p.Val845Gly) c.*28+18855T>G (n.*28+18855T>G) c.2399T>G (p.Val800Gly) c.1733T>G (p.Val578Gly) | dbSNP |
| 7 | g.55191784G>A | CA454965623 | EGFR | c.2376G>A (p.Val792=) c.884G>A c.2535G>A (p.Val845=) c.*28+18856G>A (n.*28+18856G>A) c.2400G>A (p.Val800=) c.1734G>A (p.Val578=) | |
| 7 | g.55191784G>C | CA454965624 | EGFR | c.2376G>C (p.Val792=) c.884G>C c.2535G>C (p.Val845=) c.*28+18856G>C (n.*28+18856G>C) c.2400G>C (p.Val800=) c.1734G>C (p.Val578=) | |
| 7 | g.55191784G>T | CA454965625 | EGFR | c.2376G>T (p.Val792=) c.884G>T c.2535G>T (p.Val845=) c.*28+18856G>T (n.*28+18856G>T) c.2400G>T (p.Val800=) c.1734G>T (p.Val578=) | |
| 7 | g.55191785A>C | CA367580192 | EGFR | c.2377A>C (p.Lys793Gln) c.885A>C c.2536A>C (p.Lys846Gln) c.*28+18857A>C (n.*28+18857A>C) c.2401A>C (p.Lys801Gln) c.1735A>C (p.Lys579Gln) | |
| 7 | g.55191785A>G | CA367580193 | EGFR | c.2377A>G (p.Lys793Glu) c.885A>G c.2536A>G (p.Lys846Glu) c.*28+18857A>G (n.*28+18857A>G) c.2401A>G (p.Lys801Glu) c.1735A>G (p.Lys579Glu) | dbSNP |
| 7 | g.55191785A>T | CA367580194 | EGFR | c.2377A>T (p.Lys793Ter) c.885A>T c.2536A>T (p.Lys846Ter) c.*28+18857A>T (n.*28+18857A>T) c.2401A>T (p.Lys801Ter) c.1735A>T (p.Lys579Ter) | |
| 7 | g.55191786A= | CA1708922557 | EGFR | c.2378A= (p.Lys793=) c.886A= c.2537A= (p.Lys846=) c.*28+18858A= (n.*28+18858A=) c.2402A= (p.Lys801=) c.1736A= (p.Lys579=) | |
| 7 | g.55191786A>C | CA367580197 | EGFR | c.2378A>C (p.Lys793Thr) c.886A>C c.2537A>C (p.Lys846Thr) c.*28+18858A>C (n.*28+18858A>C) c.2402A>C (p.Lys801Thr) c.1736A>C (p.Lys579Thr) | |
| 7 | g.55191786A>G | CA367580196 | EGFR | c.2378A>G (p.Lys793Arg) c.886A>G c.2537A>G (p.Lys846Arg) c.*28+18858A>G (n.*28+18858A>G) c.2402A>G (p.Lys801Arg) c.1736A>G (p.Lys579Arg) | ClinVar dbSNP COSMIC |
| 7 | g.55191786A>T | CA367580195 | EGFR | c.2378A>T (p.Lys793Ile) c.886A>T c.2537A>T (p.Lys846Ile) c.*28+18858A>T (n.*28+18858A>T) c.2402A>T (p.Lys801Ile) c.1736A>T (p.Lys579Ile) | dbSNP |
| 7 | g.55191787A>C | CA367580198 | EGFR | c.2379A>C (p.Lys793Asn) c.887A>C c.2538A>C (p.Lys846Asn) c.*28+18859A>C (n.*28+18859A>C) c.2403A>C (p.Lys801Asn) c.1737A>C (p.Lys579Asn) | dbSNP |
| 7 | g.55191787A>G | CA454965626 | EGFR | c.2379A>G (p.Lys793=) c.887A>G c.2538A>G (p.Lys846=) c.*28+18859A>G (n.*28+18859A>G) c.2403A>G (p.Lys801=) c.1737A>G (p.Lys579=) | |
| 7 | g.55191787A>T | CA367580199 | EGFR | c.2379A>T (p.Lys793Asn) c.887A>T c.2538A>T (p.Lys846Asn) c.*28+18859A>T (n.*28+18859A>T) c.2403A>T (p.Lys801Asn) c.1737A>T (p.Lys579Asn) | dbSNP |
| 7 | g.55191788A>C | CA367580200 | EGFR | c.2380A>C (p.Thr794Pro) c.888A>C c.2539A>C (p.Thr847Pro) c.*28+18860A>C (n.*28+18860A>C) c.2404A>C (p.Thr802Pro) c.1738A>C (p.Thr580Pro) | dbSNP |
| 7 | g.55191788A>G | CA367580202 | EGFR | c.2380A>G (p.Thr794Ala) c.888A>G c.2539A>G (p.Thr847Ala) c.*28+18860A>G (n.*28+18860A>G) c.2404A>G (p.Thr802Ala) c.1738A>G (p.Thr580Ala) | dbSNP |
| 7 | g.55191788A>T | CA367580201 | EGFR | c.2380A>T (p.Thr794Ser) c.888A>T c.2539A>T (p.Thr847Ser) c.*28+18860A>T (n.*28+18860A>T) c.2404A>T (p.Thr802Ser) c.1738A>T (p.Thr580Ser) | dbSNP |
| 7 | g.55191789C>A | CA367580203 | EGFR | c.2381C>A (p.Thr794Lys) c.889C>A c.2540C>A (p.Thr847Lys) c.*28+18861C>A (n.*28+18861C>A) c.2405C>A (p.Thr802Lys) c.1739C>A (p.Thr580Lys) | dbSNP |
| 7 | g.55191789C= | CA1708922559 | EGFR | c.2381C= (p.Thr794=) c.889C= c.2540C= (p.Thr847=) c.*28+18861C= (n.*28+18861C=) c.2405C= (p.Thr802=) c.1739C= (p.Thr580=) | |
| 7 | g.55191789C>G | CA367580205 | EGFR | c.2381C>G (p.Thr794Arg) c.889C>G c.2540C>G (p.Thr847Arg) c.*28+18861C>G (n.*28+18861C>G) c.2405C>G (p.Thr802Arg) c.1739C>G (p.Thr580Arg) | dbSNP |
| 7 | g.55191789C>T | CA367580204 | EGFR | c.2381C>T (p.Thr794Ile) c.889C>T c.2540C>T (p.Thr847Ile) c.*28+18861C>T (n.*28+18861C>T) c.2405C>T (p.Thr802Ile) c.1739C>T (p.Thr580Ile) | dbSNP COSMIC |
| 7 | g.55191790A>C | CA454965627 | EGFR | c.2382A>C (p.Thr794=) c.890A>C c.2541A>C (p.Thr847=) c.*28+18862A>C (n.*28+18862A>C) c.2406A>C (p.Thr802=) c.1740A>C (p.Thr580=) | dbSNP |
| 7 | g.55191790A>G | CA454965628 | EGFR | c.2382A>G (p.Thr794=) c.890A>G c.2541A>G (p.Thr847=) c.*28+18862A>G (n.*28+18862A>G) c.2406A>G (p.Thr802=) c.1740A>G (p.Thr580=) | dbSNP |
| 7 | g.55191790A>T | CA454965629 | EGFR | c.2382A>T (p.Thr794=) c.890A>T c.2541A>T (p.Thr847=) c.*28+18862A>T (n.*28+18862A>T) c.2406A>T (p.Thr802=) c.1740A>T (p.Thr580=) | dbSNP |
| 7 | g.55191791C>A | CA367580206 | EGFR | c.2383C>A (p.Pro795Thr) c.891C>A c.2542C>A (p.Pro848Thr) c.*28+18863C>A (n.*28+18863C>A) c.2407C>A (p.Pro803Thr) c.1741C>A (p.Pro581Thr) | dbSNP gnomAD v4 |
| 7 | g.55191791C= | CA1708922562 | EGFR | c.2383C= (p.Pro795=) c.891C= c.2542C= (p.Pro848=) c.*28+18863C= (n.*28+18863C=) c.2407C= (p.Pro803=) c.1741C= (p.Pro581=) | |
| 7 | g.55191791C>G | CA367580207 | EGFR | c.2383C>G (p.Pro795Ala) c.891C>G c.2542C>G (p.Pro848Ala) c.*28+18863C>G (n.*28+18863C>G) c.2407C>G (p.Pro803Ala) c.1741C>G (p.Pro581Ala) | dbSNP |
| 7 | g.55191791C>T | CA367580208 | EGFR | c.2383C>T (p.Pro795Ser) c.891C>T c.2542C>T (p.Pro848Ser) c.*28+18863C>T (n.*28+18863C>T) c.2407C>T (p.Pro803Ser) c.1741C>T (p.Pro581Ser) | ClinVar dbSNP gnomAD v4 |
| 7 | g.55191792C>A | CA367580209 | EGFR | c.2384C>A (p.Pro795Gln) c.892C>A c.2543C>A (p.Pro848Gln) c.*28+18864C>A (n.*28+18864C>A) c.2408C>A (p.Pro803Gln) c.1742C>A (p.Pro581Gln) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 7 | g.55191792C= | CA1708922568 | EGFR | c.2384C= (p.Pro795=) c.892C= c.2543C= (p.Pro848=) c.*28+18864C= (n.*28+18864C=) c.2408C= (p.Pro803=) c.1742C= (p.Pro581=) | |
| 7 | g.55191792C>G | CA367580210 | EGFR | c.2384C>G (p.Pro795Arg) c.892C>G c.2543C>G (p.Pro848Arg) c.*28+18864C>G (n.*28+18864C>G) c.2408C>G (p.Pro803Arg) c.1742C>G (p.Pro581Arg) | dbSNP |
| 7 | g.55191792C>T | CA135927 | EGFR | c.2384C>T (p.Pro795Leu) c.892C>T c.2543C>T (p.Pro848Leu) c.*28+18864C>T (n.*28+18864C>T) c.2408C>T (p.Pro803Leu) c.1742C>T (p.Pro581Leu) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 7 | g.55191793G>A | CA156276 | EGFR | c.2385G>A (p.Pro795=) c.893G>A c.2544G>A (p.Pro848=) c.*28+18865G>A (n.*28+18865G>A) c.2409G>A (p.Pro803=) c.1743G>A (p.Pro581=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 7 | g.55191793G>C | CA454965630 | EGFR | c.2385G>C (p.Pro795=) c.893G>C c.2544G>C (p.Pro848=) c.*28+18865G>C (n.*28+18865G>C) c.2409G>C (p.Pro803=) c.1743G>C (p.Pro581=) | dbSNP |
| 7 | g.55191793G= | CA1708922578 | EGFR | c.2385G= (p.Pro795=) c.893G= c.2544G= (p.Pro848=) c.*28+18865G= (n.*28+18865G=) c.2409G= (p.Pro803=) c.1743G= (p.Pro581=) | |
| 7 | g.55191793G>T | CA158934221 | EGFR | c.2385G>T (p.Pro795=) c.893G>T c.2544G>T (p.Pro848=) c.*28+18865G>T (n.*28+18865G>T) c.2409G>T (p.Pro803=) c.1743G>T (p.Pro581=) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 7 | g.55191794C>A | CA367580211 | EGFR | c.2386C>A (p.Gln796Lys) c.894C>A c.2545C>A (p.Gln849Lys) c.*28+18866C>A (n.*28+18866C>A) c.2410C>A (p.Gln804Lys) c.1744C>A (p.Gln582Lys) | dbSNP |
| 7 | g.55191794C= | CA1708922584 | EGFR | c.2386C= (p.Gln796=) c.894C= c.2545C= (p.Gln849=) c.*28+18866C= (n.*28+18866C=) c.2410C= (p.Gln804=) c.1744C= (p.Gln582=) | |
| 7 | g.55191794C>G | CA367580212 | EGFR | c.2386C>G (p.Gln796Glu) c.894C>G c.2545C>G (p.Gln849Glu) c.*28+18866C>G (n.*28+18866C>G) c.2410C>G (p.Gln804Glu) c.1744C>G (p.Gln582Glu) | dbSNP |
| 7 | g.55191794C>T | CA367580213 | EGFR | c.2386C>T (p.Gln796Ter) c.894C>T c.2545C>T (p.Gln849Ter) c.*28+18866C>T (n.*28+18866C>T) c.2410C>T (p.Gln804Ter) c.1744C>T (p.Gln582Ter) | ClinVar dbSNP gnomAD v4 |
| 7 | g.55191795A>C | CA367580216 | EGFR | c.2387A>C (p.Gln796Pro) c.895A>C c.2546A>C (p.Gln849Pro) c.*28+18867A>C (n.*28+18867A>C) c.2411A>C (p.Gln804Pro) c.1745A>C (p.Gln582Pro) | gnomAD v4 |
| 7 | g.55191795A>G | CA367580214 | EGFR | c.2387A>G (p.Gln796Arg) c.895A>G c.2546A>G (p.Gln849Arg) c.*28+18867A>G (n.*28+18867A>G) c.2411A>G (p.Gln804Arg) c.1745A>G (p.Gln582Arg) | dbSNP COSMIC |
| 7 | g.55191795A>T | CA367580215 | EGFR | c.2387A>T (p.Gln796Leu) c.895A>T c.2546A>T (p.Gln849Leu) c.*28+18867A>T (n.*28+18867A>T) c.2411A>T (p.Gln804Leu) c.1745A>T (p.Gln582Leu) | dbSNP |
| 7 | g.55191796G>A | CA454965631 | EGFR | c.2388G>A (p.Gln796=) c.896G>A c.2547G>A (p.Gln849=) c.*28+18868G>A (n.*28+18868G>A) c.2412G>A (p.Gln804=) c.1746G>A (p.Gln582=) | ClinVar dbSNP gnomAD v4 |
| 7 | g.55191796G>C | CA367580217 | EGFR | c.2388G>C (p.Gln796His) c.896G>C c.2547G>C (p.Gln849His) c.*28+18868G>C (n.*28+18868G>C) c.2412G>C (p.Gln804His) c.1746G>C (p.Gln582His) | ClinVar dbSNP gnomAD v4 |
| 7 | g.55191796G= | CA1708922589 | EGFR | c.2388G= (p.Gln796=) c.896G= c.2547G= (p.Gln849=) c.*28+18868G= (n.*28+18868G=) c.2412G= (p.Gln804=) c.1746G= (p.Gln582=) | |
| 7 | g.55191796G>T | CA367580218 | EGFR | c.2388G>T (p.Gln796His) c.896G>T c.2547G>T (p.Gln849His) c.*28+18868G>T (n.*28+18868G>T) c.2412G>T (p.Gln804His) c.1746G>T (p.Gln582His) | dbSNP gnomAD v2 gnomAD v4 |
| 7 | g.55191797C>A | CA367580219 | EGFR | c.2389C>A (p.His797Asn) c.897C>A c.2548C>A (p.His850Asn) c.*28+18869C>A (n.*28+18869C>A) c.2413C>A (p.His805Asn) c.1747C>A (p.His583Asn) | dbSNP COSMIC |
| 7 | g.55191797C>G | CA367580220 | EGFR | c.2389C>G (p.His797Asp) c.897C>G c.2548C>G (p.His850Asp) c.*28+18869C>G (n.*28+18869C>G) c.2413C>G (p.His805Asp) c.1747C>G (p.His583Asp) | dbSNP COSMIC |
| 7 | g.55191797C>T | CA367580221 | EGFR | c.2389C>T (p.His797Tyr) c.897C>T c.2548C>T (p.His850Tyr) c.*28+18869C>T (n.*28+18869C>T) c.2413C>T (p.His805Tyr) c.1747C>T (p.His583Tyr) | dbSNP COSMIC |
| 7 | g.55191798A>C | CA367580222 | EGFR | c.2390A>C (p.His797Pro) c.898A>C c.2549A>C (p.His850Pro) c.*28+18870A>C (n.*28+18870A>C) c.2414A>C (p.His805Pro) c.1748A>C (p.His583Pro) | |
| 7 | g.55191798A>G | CA367580223 | EGFR | c.2390A>G (p.His797Arg) c.898A>G c.2549A>G (p.His850Arg) c.*28+18870A>G (n.*28+18870A>G) c.2414A>G (p.His805Arg) c.1748A>G (p.His583Arg) | ClinVar dbSNP gnomAD v4 COSMIC |
| 7 | g.55191798A>T | CA367580224 | EGFR | c.2390A>T (p.His797Leu) c.898A>T c.2549A>T (p.His850Leu) c.*28+18870A>T (n.*28+18870A>T) c.2414A>T (p.His805Leu) c.1748A>T (p.His583Leu) | dbSNP gnomAD v4 |
| 7 | g.55191799T>A | CA367580225 | EGFR | c.2391T>A (p.His797Gln) c.899T>A c.2550T>A (p.His850Gln) c.*28+18871T>A (n.*28+18871T>A) c.2415T>A (p.His805Gln) c.1749T>A (p.His583Gln) | dbSNP |
| 7 | g.55191799T>C | CA454965633 | EGFR | c.2391T>C (p.His797=) c.899T>C c.2550T>C (p.His850=) c.*28+18871T>C (n.*28+18871T>C) c.2415T>C (p.His805=) c.1749T>C (p.His583=) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 7 | g.55191799T>G | CA367580226 | EGFR | c.2391T>G (p.His797Gln) c.899T>G c.2550T>G (p.His850Gln) c.*28+18871T>G (n.*28+18871T>G) c.2415T>G (p.His805Gln) c.1749T>G (p.His583Gln) | ClinVar dbSNP |
| 7 | g.55191799T= | CA1708922592 | EGFR | c.2391T= (p.His797=) c.899T= c.2550T= (p.His850=) c.*28+18871T= (n.*28+18871T=) c.2415T= (p.His805=) c.1749T= (p.His583=) | |
| 7 | g.55191800G>A | CA367580229 | EGFR | c.2392G>A (p.Val798Ile) c.899+1G>A c.2551G>A (p.Val851Ile) c.*28+18872G>A (n.*28+18872G>A) c.2416G>A (p.Val806Ile) c.1750G>A (p.Val584Ile) | dbSNP COSMIC |
| 7 | g.55191800G>C | CA367580228 | EGFR | c.2392G>C (p.Val798Leu) c.899+1G>C c.2551G>C (p.Val851Leu) c.*28+18872G>C (n.*28+18872G>C) c.2416G>C (p.Val806Leu) c.1750G>C (p.Val584Leu) | dbSNP |
| 7 | g.55191800G>T | CA367580227 | EGFR | c.2392G>T (p.Val798Phe) c.899+1G>T c.2551G>T (p.Val851Phe) c.*28+18872G>T (n.*28+18872G>T) c.2416G>T (p.Val806Phe) c.1750G>T (p.Val584Phe) | dbSNP |
| 7 | g.55191801T>A | CA367580230 | EGFR | c.2393T>A (p.Val798Asp) c.899+2T>A c.2552T>A (p.Val851Asp) c.*28+18873T>A (n.*28+18873T>A) c.2417T>A (p.Val806Asp) c.1751T>A (p.Val584Asp) | dbSNP |
| 7 | g.55191801T>C | CA367580231 | EGFR | c.2393T>C (p.Val798Ala) c.899+2T>C c.2552T>C (p.Val851Ala) c.*28+18873T>C (n.*28+18873T>C) c.2417T>C (p.Val806Ala) c.1751T>C (p.Val584Ala) | dbSNP COSMIC |
| 7 | g.55191801T>G | CA367580232 | EGFR | c.2393T>G (p.Val798Gly) c.899+2T>G c.2552T>G (p.Val851Gly) c.*28+18873T>G (n.*28+18873T>G) c.2417T>G (p.Val806Gly) c.1751T>G (p.Val584Gly) | dbSNP |
| 7 | g.55191802C>A | CA454965636 | EGFR | c.2394C>A (p.Val798=) c.899+3C>A c.2553C>A (p.Val851=) c.*28+18874C>A (n.*28+18874C>A) c.2418C>A (p.Val806=) c.1752C>A (p.Val584=) | dbSNP |
| 7 | g.55191802C>G | CA454965634 | EGFR | c.2394C>G (p.Val798=) c.899+3C>G c.2553C>G (p.Val851=) c.*28+18874C>G (n.*28+18874C>G) c.2418C>G (p.Val806=) c.1752C>G (p.Val584=) | dbSNP gnomAD v4 |
| 7 | g.55191802C>T | CA454965635 | EGFR | c.2394C>T (p.Val798=) c.899+3C>T c.2553C>T (p.Val851=) c.*28+18874C>T (n.*28+18874C>T) c.2418C>T (p.Val806=) c.1752C>T (p.Val584=) | dbSNP |
| 7 | g.55191803A>C | CA367580233 | EGFR | c.2395A>C (p.Lys799Gln) c.899+4A>C c.2554A>C (p.Lys852Gln) c.*28+18875A>C (n.*28+18875A>C) c.2419A>C (p.Lys807Gln) c.1753A>C (p.Lys585Gln) | |
| 7 | g.55191803A>G | CA367580234 | EGFR | c.2395A>G (p.Lys799Glu) c.899+4A>G c.2554A>G (p.Lys852Glu) c.*28+18875A>G (n.*28+18875A>G) c.2419A>G (p.Lys807Glu) c.1753A>G (p.Lys585Glu) | dbSNP |
| 7 | g.55191803A>T | CA367580235 | EGFR | c.2395A>T (p.Lys799Ter) c.899+4A>T c.2554A>T (p.Lys852Ter) c.*28+18875A>T (n.*28+18875A>T) c.2419A>T (p.Lys807Ter) c.1753A>T (p.Lys585Ter) | dbSNP |
| 7 | g.55191804A= | CA1708922595 | EGFR | c.2396A= (p.Lys799=) c.899+5A= c.2555A= (p.Lys852=) c.*28+18876A= (n.*28+18876A=) c.2420A= (p.Lys807=) c.1754A= (p.Lys585=) | |
| 7 | g.55191804A>C | CA367580236 | EGFR | c.2396A>C (p.Lys799Thr) c.899+5A>C c.2555A>C (p.Lys852Thr) c.*28+18876A>C (n.*28+18876A>C) c.2420A>C (p.Lys807Thr) c.1754A>C (p.Lys585Thr) | |
| 7 | g.55191804A>G | CA367580237 | EGFR | c.2396A>G (p.Lys799Arg) c.899+5A>G c.2555A>G (p.Lys852Arg) c.*28+18876A>G (n.*28+18876A>G) c.2420A>G (p.Lys807Arg) c.1754A>G (p.Lys585Arg) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 7 | g.55191804A>T | CA367580238 | EGFR | c.2396A>T (p.Lys799Met) c.899+5A>T c.2555A>T (p.Lys852Met) c.*28+18876A>T (n.*28+18876A>T) c.2420A>T (p.Lys807Met) c.1754A>T (p.Lys585Met) | dbSNP |
| 7 | g.55191805G>A | CA454965637 | EGFR | c.2397G>A (p.Lys799=) c.899+6G>A c.2556G>A (p.Lys852=) c.*28+18877G>A (n.*28+18877G>A) c.2421G>A (p.Lys807=) c.1755G>A (p.Lys585=) | dbSNP gnomAD v2 gnomAD v4 |
| 7 | g.55191805G>C | CA367580239 | EGFR | c.2397G>C (p.Lys799Asn) c.899+6G>C c.2556G>C (p.Lys852Asn) c.*28+18877G>C (n.*28+18877G>C) c.2421G>C (p.Lys807Asn) c.1755G>C (p.Lys585Asn) | ClinVar dbSNP gnomAD v4 |
| 7 | g.55191805G= | CA1708922599 | EGFR | c.2397G= (p.Lys799=) c.899+6G= c.2556G= (p.Lys852=) c.*28+18877G= (n.*28+18877G=) c.2421G= (p.Lys807=) c.1755G= (p.Lys585=) | |
| 7 | g.55191805G>T | CA367580240 | EGFR | c.2397G>T (p.Lys799Asn) c.899+6G>T c.2556G>T (p.Lys852Asn) c.*28+18877G>T (n.*28+18877G>T) c.2421G>T (p.Lys807Asn) c.1755G>T (p.Lys585Asn) | dbSNP COSMIC |
| 7 | g.55191806A>C | CA367580243 | EGFR | c.2398A>C (p.Ile800Leu) c.899+7A>C c.2557A>C (p.Ile853Leu) c.*28+18878A>C (n.*28+18878A>C) c.2422A>C (p.Ile808Leu) c.1756A>C (p.Ile586Leu) | dbSNP |
| 7 | g.55191806A>G | CA367580242 | EGFR | c.2398A>G (p.Ile800Val) c.899+7A>G c.2557A>G (p.Ile853Val) c.*28+18878A>G (n.*28+18878A>G) c.2422A>G (p.Ile808Val) c.1756A>G (p.Ile586Val) | |
| 7 | g.55191806A>T | CA367580241 | EGFR | c.2398A>T (p.Ile800Phe) c.899+7A>T c.2557A>T (p.Ile853Phe) c.*28+18878A>T (n.*28+18878A>T) c.2422A>T (p.Ile808Phe) c.1756A>T (p.Ile586Phe) | |
| 7 | g.55191807T>A | CA367580244 | EGFR | c.2399T>A (p.Ile800Asn) c.899+8T>A c.2558T>A (p.Ile853Asn) c.*28+18879T>A (n.*28+18879T>A) c.2423T>A (p.Ile808Asn) c.1757T>A (p.Ile586Asn) | dbSNP |
| 7 | g.55191807T>C | CA367580245 | EGFR | c.2399T>C (p.Ile800Thr) c.899+8T>C c.2558T>C (p.Ile853Thr) c.*28+18879T>C (n.*28+18879T>C) c.2423T>C (p.Ile808Thr) c.1757T>C (p.Ile586Thr) | COSMIC |
| 7 | g.55191807T>G | CA367580246 | EGFR | c.2399T>G (p.Ile800Ser) c.899+8T>G c.2558T>G (p.Ile853Ser) c.*28+18879T>G (n.*28+18879T>G) c.2423T>G (p.Ile808Ser) c.1757T>G (p.Ile586Ser) | dbSNP |
| 7 | g.55191808C>A | CA454965638 | EGFR | c.2400C>A (p.Ile800=) c.899+9C>A c.2559C>A (p.Ile853=) c.*28+18880C>A (n.*28+18880C>A) c.2424C>A (p.Ile808=) c.1758C>A (p.Ile586=) | dbSNP gnomAD v4 |
| 7 | g.55191808C>G | CA367580247 | EGFR | c.2400C>G (p.Ile800Met) c.899+9C>G c.2559C>G (p.Ile853Met) c.*28+18880C>G (n.*28+18880C>G) c.2424C>G (p.Ile808Met) c.1758C>G (p.Ile586Met) | dbSNP |
| 7 | g.55191808C>T | CA454965640 | EGFR | c.2400C>T (p.Ile800=) c.899+9C>T c.2559C>T (p.Ile853=) c.*28+18880C>T (n.*28+18880C>T) c.2424C>T (p.Ile808=) c.1758C>T (p.Ile586=) | dbSNP COSMIC |
| 7 | g.55191809A= | CA1708922602 | EGFR | c.2401A= (p.Thr801=) c.899+10A= c.2560A= (p.Thr854=) c.*28+18881A= (n.*28+18881A=) c.2425A= (p.Thr809=) c.1759A= (p.Thr587=) | |
| 7 | g.55191809A>C | CA367580248 | EGFR | c.2401A>C (p.Thr801Pro) c.899+10A>C c.2560A>C (p.Thr854Pro) c.*28+18881A>C (n.*28+18881A>C) c.2425A>C (p.Thr809Pro) c.1759A>C (p.Thr587Pro) | dbSNP COSMIC |
| 7 | g.55191809A>G | CA367580249 | EGFR | c.2401A>G (p.Thr801Ala) c.899+10A>G c.2560A>G (p.Thr854Ala) c.*28+18881A>G (n.*28+18881A>G) c.2425A>G (p.Thr809Ala) c.1759A>G (p.Thr587Ala) | ClinVar dbSNP COSMIC |
| 7 | g.55191809A>T | CA367580250 | EGFR | c.2401A>T (p.Thr801Ser) c.899+10A>T c.2560A>T (p.Thr854Ser) c.*28+18881A>T (n.*28+18881A>T) c.2425A>T (p.Thr809Ser) c.1759A>T (p.Thr587Ser) | dbSNP COSMIC |
| 7 | g.55191810C>A | CA367580251 | EGFR | c.2402C>A (p.Thr801Lys) c.899+11C>A c.2561C>A (p.Thr854Lys) c.*28+18882C>A (n.*28+18882C>A) c.2426C>A (p.Thr809Lys) c.1760C>A (p.Thr587Lys) | dbSNP |
| 7 | g.55191810C>G | CA367580252 | EGFR | c.2402C>G (p.Thr801Arg) c.899+11C>G c.2561C>G (p.Thr854Arg) c.*28+18882C>G (n.*28+18882C>G) c.2426C>G (p.Thr809Arg) c.1760C>G (p.Thr587Arg) | dbSNP |
| 7 | g.55191810C>T | CA367580253 | EGFR | c.2402C>T (p.Thr801Ile) c.899+11C>T c.2561C>T (p.Thr854Ile) c.*28+18882C>T (n.*28+18882C>T) c.2426C>T (p.Thr809Ile) c.1760C>T (p.Thr587Ile) | ClinVar dbSNP COSMIC |
| 7 | g.55191811A>C | CA454965641 | EGFR | c.2403A>C (p.Thr801=) c.899+12A>C c.2562A>C (p.Thr854=) c.*28+18883A>C (n.*28+18883A>C) c.2427A>C (p.Thr809=) c.1761A>C (p.Thr587=) | |
| 7 | g.55191811A>G | CA454965642 | EGFR | c.2403A>G (p.Thr801=) c.899+12A>G c.2562A>G (p.Thr854=) c.*28+18883A>G (n.*28+18883A>G) c.2427A>G (p.Thr809=) c.1761A>G (p.Thr587=) | |
| 7 | g.55191811A>T | CA454965643 | EGFR | c.2403A>T (p.Thr801=) c.899+12A>T c.2562A>T (p.Thr854=) c.*28+18883A>T (n.*28+18883A>T) c.2427A>T (p.Thr809=) c.1761A>T (p.Thr587=) | dbSNP |
| 7 | g.55191812G>A | CA367580254 | EGFR | c.2404G>A (p.Asp802Asn) c.899+13G>A c.2563G>A (p.Asp855Asn) c.*28+18884G>A (n.*28+18884G>A) c.2428G>A (p.Asp810Asn) c.1762G>A (p.Asp588Asn) | dbSNP COSMIC |
| 7 | g.55191812G>C | CA367580255 | EGFR | c.2404G>C (p.Asp802His) c.899+13G>C c.2563G>C (p.Asp855His) c.*28+18884G>C (n.*28+18884G>C) c.2428G>C (p.Asp810His) c.1762G>C (p.Asp588His) | dbSNP |
| 7 | g.55191812G>T | CA367580256 | EGFR | c.2404G>T (p.Asp802Tyr) c.899+13G>T c.2563G>T (p.Asp855Tyr) c.*28+18884G>T (n.*28+18884G>T) c.2428G>T (p.Asp810Tyr) c.1762G>T (p.Asp588Tyr) | |
| 7 | g.55191813A>C | CA367580258 | EGFR | c.2405A>C (p.Asp802Ala) c.899+14A>C c.2564A>C (p.Asp855Ala) c.*28+18885A>C (n.*28+18885A>C) c.2429A>C (p.Asp810Ala) c.1763A>C (p.Asp588Ala) | |
| 7 | g.55191813A>G | CA367580259 | EGFR | c.2405A>G (p.Asp802Gly) c.899+14A>G c.2564A>G (p.Asp855Gly) c.*28+18885A>G (n.*28+18885A>G) c.2429A>G (p.Asp810Gly) c.1763A>G (p.Asp588Gly) | COSMIC |
| 7 | g.55191813A>T | CA367580257 | EGFR | c.2405A>T (p.Asp802Val) c.899+14A>T c.2564A>T (p.Asp855Val) c.*28+18885A>T (n.*28+18885A>T) c.2429A>T (p.Asp810Val) c.1763A>T (p.Asp588Val) | |
| 7 | g.55191814T>A | CA367580261 | EGFR | c.2406T>A (p.Asp802Glu) c.899+15T>A c.2565T>A (p.Asp855Glu) c.*28+18886T>A (n.*28+18886T>A) c.2430T>A (p.Asp810Glu) c.1764T>A (p.Asp588Glu) | dbSNP |
| 7 | g.55191814T>C | CA454965644 | EGFR | c.2406T>C (p.Asp802=) c.899+15T>C c.2565T>C (p.Asp855=) c.*28+18886T>C (n.*28+18886T>C) c.2430T>C (p.Asp810=) c.1764T>C (p.Asp588=) | |
| 7 | g.55191814T>G | CA367580260 | EGFR | c.2406T>G (p.Asp802Glu) c.899+15T>G c.2565T>G (p.Asp855Glu) c.*28+18886T>G (n.*28+18886T>G) c.2430T>G (p.Asp810Glu) c.1764T>G (p.Asp588Glu) | dbSNP |
| 7 | g.55191815T>A | CA367580262 | EGFR | c.2407T>A (p.Phe803Ile) c.899+16T>A c.2566T>A (p.Phe856Ile) c.*28+18887T>A (n.*28+18887T>A) c.2431T>A (p.Phe811Ile) c.1765T>A (p.Phe589Ile) | dbSNP |
| 7 | g.55191815T>C | CA367580263 | EGFR | c.2407T>C (p.Phe803Leu) c.899+16T>C c.2566T>C (p.Phe856Leu) c.*28+18887T>C (n.*28+18887T>C) c.2431T>C (p.Phe811Leu) c.1765T>C (p.Phe589Leu) | dbSNP |
| 7 | g.55191815T>G | CA367580264 | EGFR | c.2407T>G (p.Phe803Val) c.899+16T>G c.2566T>G (p.Phe856Val) c.*28+18887T>G (n.*28+18887T>G) c.2431T>G (p.Phe811Val) c.1765T>G (p.Phe589Val) | gnomAD v4 |
| 7 | g.55191816T>A | CA367580265 | EGFR | c.2408T>A (p.Phe803Tyr) c.899+17T>A c.2567T>A (p.Phe856Tyr) c.*28+18888T>A (n.*28+18888T>A) c.2432T>A (p.Phe811Tyr) c.1766T>A (p.Phe589Tyr) | dbSNP |
| 7 | g.55191816T>C | CA367580266 | EGFR | c.2408T>C (p.Phe803Ser) c.899+17T>C c.2567T>C (p.Phe856Ser) c.*28+18888T>C (n.*28+18888T>C) c.2432T>C (p.Phe811Ser) c.1766T>C (p.Phe589Ser) | dbSNP COSMIC |
| 7 | g.55191816T>G | CA367580267 | EGFR | c.2408T>G (p.Phe803Cys) c.899+17T>G c.2567T>G (p.Phe856Cys) c.*28+18888T>G (n.*28+18888T>G) c.2432T>G (p.Phe811Cys) c.1766T>G (p.Phe589Cys) | dbSNP |
| 7 | g.55191817T>A | CA367580268 | EGFR | c.2409T>A (p.Phe803Leu) c.899+18T>A c.2568T>A (p.Phe856Leu) c.*28+18889T>A (n.*28+18889T>A) c.2433T>A (p.Phe811Leu) c.1767T>A (p.Phe589Leu) | |
| 7 | g.55191817T>C | CA4266113 | EGFR | c.2409T>C (p.Phe803=) c.899+18T>C c.2568T>C (p.Phe856=) c.*28+18889T>C (n.*28+18889T>C) c.2433T>C (p.Phe811=) c.1767T>C (p.Phe589=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 7 | g.55191817T>G | CA367580269 | EGFR | c.2409T>G (p.Phe803Leu) c.899+18T>G c.2568T>G (p.Phe856Leu) c.*28+18889T>G (n.*28+18889T>G) c.2433T>G (p.Phe811Leu) c.1767T>G (p.Phe589Leu) | COSMIC |
| 7 | g.55191817T= | CA1708922605 | EGFR | c.2409T= (p.Phe803=) c.899+18T= c.2568T= (p.Phe856=) c.*28+18889T= (n.*28+18889T=) c.2433T= (p.Phe811=) c.1767T= (p.Phe589=) | |
| 7 | g.55191818G>A | CA367580270 | EGFR | c.2410G>A (p.Gly804Arg) c.899+19G>A c.2569G>A (p.Gly857Arg) c.*28+18890G>A (n.*28+18890G>A) c.2434G>A (p.Gly812Arg) c.1768G>A (p.Gly590Arg) | dbSNP COSMIC |
| 7 | g.55191818G>C | CA367580271 | EGFR | c.2410G>C (p.Gly804Arg) c.899+19G>C c.2569G>C (p.Gly857Arg) c.*28+18890G>C (n.*28+18890G>C) c.2434G>C (p.Gly812Arg) c.1768G>C (p.Gly590Arg) | dbSNP |
| 7 | g.55191818G>T | CA367580272 | EGFR | c.2410G>T (p.Gly804Trp) c.899+19G>T c.2569G>T (p.Gly857Trp) c.*28+18890G>T (n.*28+18890G>T) c.2434G>T (p.Gly812Trp) c.1768G>T (p.Gly590Trp) | dbSNP |
| 7 | g.55191819G>A | CA367580273 | EGFR | c.2411G>A (p.Gly804Glu) c.899+20G>A c.2570G>A (p.Gly857Glu) c.*28+18891G>A (n.*28+18891G>A) c.2435G>A (p.Gly812Glu) c.1769G>A (p.Gly590Glu) | dbSNP COSMIC |
| 7 | g.55191819G>C | CA367580275 | EGFR | c.2411G>C (p.Gly804Ala) c.899+20G>C c.2570G>C (p.Gly857Ala) c.*28+18891G>C (n.*28+18891G>C) c.2435G>C (p.Gly812Ala) c.1769G>C (p.Gly590Ala) | dbSNP |
| 7 | g.55191819G>T | CA367580274 | EGFR | c.2411G>T (p.Gly804Val) c.899+20G>T c.2570G>T (p.Gly857Val) c.*28+18891G>T (n.*28+18891G>T) c.2435G>T (p.Gly812Val) c.1769G>T (p.Gly590Val) | dbSNP COSMIC |
| 7 | g.55191820G>A | CA454965645 | EGFR | c.2412G>A (p.Gly804=) c.899+21G>A c.2571G>A (p.Gly857=) c.*28+18892G>A (n.*28+18892G>A) c.2436G>A (p.Gly812=) c.1770G>A (p.Gly590=) | ClinVar dbSNP gnomAD v4 |
| 7 | g.55191820G>C | CA454965646 | EGFR | c.2412G>C (p.Gly804=) c.899+21G>C c.2571G>C (p.Gly857=) c.*28+18892G>C (n.*28+18892G>C) c.2436G>C (p.Gly812=) c.1770G>C (p.Gly590=) | dbSNP |
| 7 | g.55191820G>T | CA454965647 | EGFR | c.2412G>T (p.Gly804=) c.899+21G>T c.2571G>T (p.Gly857=) c.*28+18892G>T (n.*28+18892G>T) c.2436G>T (p.Gly812=) c.1770G>T (p.Gly590=) | ClinVar dbSNP |
| 7 | g.55191821C>A | CA135930 | EGFR | c.2413C>A (p.Leu805Met) c.899+22C>A c.2572C>A (p.Leu858Met) c.*28+18893C>A (n.*28+18893C>A) c.2437C>A (p.Leu813Met) c.1771C>A (p.Leu591Met) | ClinVar dbSNP COSMIC |
| 7 | g.55191821C= | CA1708922607 | EGFR | c.2413C= (p.Leu805=) c.899+22C= c.2572C= (p.Leu858=) c.*28+18893C= (n.*28+18893C=) c.2437C= (p.Leu813=) c.1771C= (p.Leu591=) | |
| 7 | g.55191821C>G | CA367580276 | EGFR | c.2413C>G (p.Leu805Val) c.899+22C>G c.2572C>G (p.Leu858Val) c.*28+18893C>G (n.*28+18893C>G) c.2437C>G (p.Leu813Val) c.1771C>G (p.Leu591Val) | |
| 7 | g.55191821C>T | CA135933 | EGFR | c.2413C>T (p.Leu805=) c.899+22C>T c.2572C>T (p.Leu858=) c.*28+18893C>T (n.*28+18893C>T) c.2437C>T (p.Leu813=) c.1771C>T (p.Leu591=) | ClinVar dbSNP gnomAD v3 gnomAD v4 COSMIC |
| 7 | g.55191821_55191822delinsAA | CA645561612 | EGFR | c.2413_2414delinsAA (p.Leu805Lys) c.899+22_899+23delinsAA c.2572_2573delinsAA (p.Leu858Lys) c.*28+18893_*28+18894delinsAA (n.*28+18893_*28+18894delinsAA) c.2437_2438delinsAA (p.Leu813Lys) c.1771_1772delinsAA (p.Leu591Lys) | dbSNP COSMIC |
| 7 | g.55191821_55191822delinsAG | CA16602728 | EGFR | c.2413_2414delinsAG (p.Leu805Arg) c.899+22_899+23delinsAG c.2572_2573delinsAG (p.Leu858Arg) c.*28+18893_*28+18894delinsAG (n.*28+18893_*28+18894delinsAG) c.2437_2438delinsAG (p.Leu813Arg) c.1771_1772delinsAG (p.Leu591Arg) | ClinVar dbSNP COSMIC |
| 7 | g.55191821_55191822delinsCT | CA1708922610 | EGFR | c.2413_2414delinsCT (p.Leu805=) c.899+22_899+23delinsCT c.2572_2573delinsCT (p.Leu858=) c.*28+18893_*28+18894delinsCT (n.*28+18893_*28+18894delinsCT) c.2437_2438delinsCT (p.Leu813=) c.1771_1772delinsCT (p.Leu591=) | |
| 7 | g.55191822T>A | CA16602729 | EGFR | c.2414T>A (p.Leu805Gln) c.899+23T>A c.2573T>A (p.Leu858Gln) c.*28+18894T>A (n.*28+18894T>A) c.2438T>A (p.Leu813Gln) c.1772T>A (p.Leu591Gln) | ClinVar dbSNP COSMIC |
| 7 | g.55191822T>C | CA367580277 | EGFR | c.2414T>C (p.Leu805Pro) c.899+23T>C c.2573T>C (p.Leu858Pro) c.*28+18894T>C (n.*28+18894T>C) c.2438T>C (p.Leu813Pro) c.1772T>C (p.Leu591Pro) | |
| 7 | g.55191822T>G | CA126713 | EGFR | c.2414T>G (p.Leu805Arg) c.899+23T>G c.2573T>G (p.Leu858Arg) c.*28+18894T>G (n.*28+18894T>G) c.2438T>G (p.Leu813Arg) c.1772T>G (p.Leu591Arg) | ClinVar dbSNP COSMIC |
| 7 | g.55191822T= | CA1708922630 | EGFR | c.2414T= (p.Leu805=) c.899+23T= c.2573T= (p.Leu858=) c.*28+18894T= (n.*28+18894T=) c.2438T= (p.Leu813=) c.1772T= (p.Leu591=) | |
| 7 | g.55191822_55191823delinsGA | CA645561613 | EGFR | c.2414_2415delinsGA (p.Leu805Arg) c.899+23_899+24delinsGA c.2573_2574delinsGA (p.Leu858Arg) c.*28+18894_*28+18895delinsGA (n.*28+18894_*28+18895delinsGA) c.2438_2439delinsGA (p.Leu813Arg) c.1772_1773delinsGA (p.Leu591Arg) | dbSNP COSMIC |
| 7 | g.55191822_55191823delinsGT | CA16602730 | EGFR | c.2414_2415delinsGT (p.Leu805Arg) c.899+23_899+24delinsGT c.2573_2574delinsGT (p.Leu858Arg) c.*28+18894_*28+18895delinsGT (n.*28+18894_*28+18895delinsGT) c.2438_2439delinsGT (p.Leu813Arg) c.1772_1773delinsGT (p.Leu591Arg) | ClinVar dbSNP COSMIC |
| 7 | g.55191822_55191823delinsTG | CA1708922627 | EGFR | c.2414_2415delinsTG (p.Leu805=) c.899+23_899+24delinsTG c.2573_2574delinsTG (p.Leu858=) c.*28+18894_*28+18895delinsTG (n.*28+18894_*28+18895delinsTG) c.2438_2439delinsTG (p.Leu813=) c.1772_1773delinsTG (p.Leu591=) | |
| 7 | g.55191823G>A | CA4266114 | EGFR | c.2415G>A (p.Leu805=) c.899+24G>A c.2574G>A (p.Leu858=) c.*28+18895G>A (n.*28+18895G>A) c.2439G>A (p.Leu813=) c.1773G>A (p.Leu591=) | dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC |
| 7 | g.55191823G>C | CA454965648 | EGFR | c.2415G>C (p.Leu805=) c.899+24G>C c.2574G>C (p.Leu858=) c.*28+18895G>C (n.*28+18895G>C) c.2439G>C (p.Leu813=) c.1773G>C (p.Leu591=) | dbSNP |
| 7 | g.55191823G= | CA1708922635 | EGFR | c.2415G= (p.Leu805=) c.899+24G= c.2574G= (p.Leu858=) c.*28+18895G= (n.*28+18895G=) c.2439G= (p.Leu813=) c.1773G= (p.Leu591=) | |
| 7 | g.55191823G>T | CA135936 | EGFR | c.2415G>T (p.Leu805=) c.899+24G>T c.2574G>T (p.Leu858=) c.*28+18895G>T (n.*28+18895G>T) c.2439G>T (p.Leu813=) c.1773G>T (p.Leu591=) | ClinVar dbSNP |
| 7 | g.55191824dup | CA645561614 | EGFR | c.2416dup (p.Ala806GlyfsTer?) c.899+25dup c.2575dup (p.Ala859GlyfsTer?) c.*28+18896dup (n.*28+18896dup) c.2440dup (p.Ala814GlyfsTer?) c.1774dup (p.Ala592GlyfsTer?) | COSMIC |
| 7 | g.55191824G>A | CA367580278 | EGFR | c.2416G>A (p.Ala806Thr) c.899+25G>A c.2575G>A (p.Ala859Thr) c.*28+18896G>A (n.*28+18896G>A) c.2440G>A (p.Ala814Thr) c.1774G>A (p.Ala592Thr) | gnomAD v4 COSMIC |
| 7 | g.55191824G>C | CA367580279 | EGFR | c.2416G>C (p.Ala806Pro) c.899+25G>C c.2575G>C (p.Ala859Pro) c.*28+18896G>C (n.*28+18896G>C) c.2440G>C (p.Ala814Pro) c.1774G>C (p.Ala592Pro) | |
| 7 | g.55191824G>T | CA367580280 | EGFR | c.2416G>T (p.Ala806Ser) c.899+25G>T c.2575G>T (p.Ala859Ser) c.*28+18896G>T (n.*28+18896G>T) c.2440G>T (p.Ala814Ser) c.1774G>T (p.Ala592Ser) | ClinVar dbSNP |
| 7 | g.55191824_55191825delinsGC | CA1708922644 | EGFR | c.2416_2417delinsGC (p.Ala806=) c.899+25_899+26delinsGC c.2575_2576delinsGC (p.Ala859=) c.*28+18896_*28+18897delinsGC (n.*28+18896_*28+18897delinsGC) c.2440_2441delinsGC (p.Ala814=) c.1774_1775delinsGC (p.Ala592=) | |
| 7 | g.55191825C>A | CA367580281 | EGFR | c.2417C>A (p.Ala806Asp) c.899+26C>A c.2576C>A (p.Ala859Asp) c.*28+18897C>A (n.*28+18897C>A) c.2441C>A (p.Ala814Asp) c.1775C>A (p.Ala592Asp) | dbSNP COSMIC |
| 7 | g.55191825C= | CA1708922648 | EGFR | c.2417C= (p.Ala806=) c.899+26C= c.2576C= (p.Ala859=) c.*28+18897C= (n.*28+18897C=) c.2441C= (p.Ala814=) c.1775C= (p.Ala592=) | |
| 7 | g.55191825C>G | CA367580282 | EGFR | c.2417C>G (p.Ala806Gly) c.899+26C>G c.2576C>G (p.Ala859Gly) c.*28+18897C>G (n.*28+18897C>G) c.2441C>G (p.Ala814Gly) c.1775C>G (p.Ala592Gly) | dbSNP |
| 7 | g.55191825C>T | CA4266115 | EGFR | c.2417C>T (p.Ala806Val) c.899+26C>T c.2576C>T (p.Ala859Val) c.*28+18897C>T (n.*28+18897C>T) c.2441C>T (p.Ala814Val) c.1775C>T (p.Ala592Val) | dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC |
| 7 | g.55191826del | CA1708922646 | EGFR | c.2418del (p.Lys807AsnfsTer?) c.899+27del c.2577del (p.Lys860AsnfsTer?) c.*28+18898del (n.*28+18898del) c.2442del (p.Lys815AsnfsTer?) c.1776del (p.Lys593AsnfsTer?) | ClinVar dbSNP gnomAD v4 |
| 7 | g.55191825_55191826insG | CA454965649 | EGFR | c.2417_2418insG (p.Lys807GlnfsTer?) c.899+26_899+27insG c.2576_2577insG (p.Lys860GlnfsTer?) c.*28+18897_*28+18898insG (n.*28+18897_*28+18898insG) c.2441_2442insG (p.Lys815GlnfsTer?) c.1775_1776insG (p.Lys593GlnfsTer?) | |
| 7 | g.55191826C>A | CA158934264 | EGFR | c.2418C>A (p.Ala806=) c.899+27C>A c.2577C>A (p.Ala859=) c.*28+18898C>A (n.*28+18898C>A) c.2442C>A (p.Ala814=) c.1776C>A (p.Ala592=) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 7 | g.55191826C= | CA1708922650 | EGFR | c.2418C= (p.Ala806=) c.899+27C= c.2577C= (p.Ala859=) c.*28+18898C= (n.*28+18898C=) c.2442C= (p.Ala814=) c.1776C= (p.Ala592=) | |
| 7 | g.55191826C>G | CA454965650 | EGFR | c.2418C>G (p.Ala806=) c.899+27C>G c.2577C>G (p.Ala859=) c.*28+18898C>G (n.*28+18898C>G) c.2442C>G (p.Ala814=) c.1776C>G (p.Ala592=) | dbSNP |
| 7 | g.55191826C>T | CA454965651 | EGFR | c.2418C>T (p.Ala806=) c.899+27C>T c.2577C>T (p.Ala859=) c.*28+18898C>T (n.*28+18898C>T) c.2442C>T (p.Ala814=) c.1776C>T (p.Ala592=) | dbSNP |
| 7 | g.55191827A>C | CA367580283 | EGFR | c.2419A>C (p.Lys807Gln) c.899+28A>C c.2578A>C (p.Lys860Gln) c.*28+18899A>C (n.*28+18899A>C) c.2443A>C (p.Lys815Gln) c.1777A>C (p.Lys593Gln) | |
| 7 | g.55191827A>G | CA367580284 | EGFR | c.2419A>G (p.Lys807Glu) c.899+28A>G c.2578A>G (p.Lys860Glu) c.*28+18899A>G (n.*28+18899A>G) c.2443A>G (p.Lys815Glu) c.1777A>G (p.Lys593Glu) | dbSNP |
| 7 | g.55191827A>T | CA367580285 | EGFR | c.2419A>T (p.Lys807Ter) c.899+28A>T c.2578A>T (p.Lys860Ter) c.*28+18899A>T (n.*28+18899A>T) c.2443A>T (p.Lys815Ter) c.1777A>T (p.Lys593Ter) | dbSNP |
| 7 | g.55191828A>C | CA367580286 | EGFR | c.2420A>C (p.Lys807Thr) c.899+29A>C c.2579A>C (p.Lys860Thr) c.*28+18900A>C (n.*28+18900A>C) c.2444A>C (p.Lys815Thr) c.1778A>C (p.Lys593Thr) | dbSNP |
| 7 | g.55191828A>G | CA367580287 | EGFR | c.2420A>G (p.Lys807Arg) c.899+29A>G c.2579A>G (p.Lys860Arg) c.*28+18900A>G (n.*28+18900A>G) c.2444A>G (p.Lys815Arg) c.1778A>G (p.Lys593Arg) | dbSNP |
| 7 | g.55191828A>T | CA367580288 | EGFR | c.2420A>T (p.Lys807Ile) c.899+29A>T c.2579A>T (p.Lys860Ile) c.*28+18900A>T (n.*28+18900A>T) c.2444A>T (p.Lys815Ile) c.1778A>T (p.Lys593Ile) | dbSNP COSMIC |
| 7 | g.55191829A= | CA1708922653 | EGFR | c.2421A= (p.Lys807=) c.899+30A= c.2580A= (p.Lys860=) c.*28+18901A= (n.*28+18901A=) c.2445A= (p.Lys815=) c.1779A= (p.Lys593=) | |
| 7 | g.55191829A>C | CA367580289 | EGFR | c.2421A>C (p.Lys807Asn) c.899+30A>C c.2580A>C (p.Lys860Asn) c.*28+18901A>C (n.*28+18901A>C) c.2445A>C (p.Lys815Asn) c.1779A>C (p.Lys593Asn) | dbSNP |
| 7 | g.55191829A>G | CA454965652 | EGFR | c.2421A>G (p.Lys807=) c.899+30A>G c.2580A>G (p.Lys860=) c.*28+18901A>G (n.*28+18901A>G) c.2445A>G (p.Lys815=) c.1779A>G (p.Lys593=) | ClinVar dbSNP |
| 7 | g.55191829A>T | CA135937 | EGFR | c.2421A>T (p.Lys807Asn) c.899+30A>T c.2580A>T (p.Lys860Asn) c.*28+18901A>T (n.*28+18901A>T) c.2445A>T (p.Lys815Asn) c.1779A>T (p.Lys593Asn) | ClinVar dbSNP |
| 7 | g.55191830C>A | CA367580290 | EGFR | c.2422C>A (p.Leu808Met) c.899+31C>A c.2581C>A (p.Leu861Met) c.*28+18902C>A (n.*28+18902C>A) c.2446C>A (p.Leu816Met) c.1780C>A (p.Leu594Met) | dbSNP |
| 7 | g.55191830C>G | CA367580291 | EGFR | c.2422C>G (p.Leu808Val) c.899+31C>G c.2581C>G (p.Leu861Val) c.*28+18902C>G (n.*28+18902C>G) c.2446C>G (p.Leu816Val) c.1780C>G (p.Leu594Val) | dbSNP COSMIC |
| 7 | g.55191830C>T | CA454965653 | EGFR | c.2422C>T (p.Leu808=) c.899+31C>T c.2581C>T (p.Leu861=) c.*28+18902C>T (n.*28+18902C>T) c.2446C>T (p.Leu816=) c.1780C>T (p.Leu594=) | dbSNP COSMIC |
| 7 | g.55191831T>A | CA176021 | EGFR | c.2423T>A (p.Leu808Gln) c.899+32T>A c.2582T>A (p.Leu861Gln) c.*28+18903T>A (n.*28+18903T>A) c.2447T>A (p.Leu816Gln) c.1781T>A (p.Leu594Gln) | ClinVar dbSNP COSMIC |
| 7 | g.55191831T>C | CA16602602 | EGFR | c.2423T>C (p.Leu808Pro) c.899+32T>C c.2582T>C (p.Leu861Pro) c.*28+18903T>C (n.*28+18903T>C) c.2447T>C (p.Leu816Pro) c.1781T>C (p.Leu594Pro) | ClinVar dbSNP |
| 7 | g.55191831T>G | CA135940 | EGFR | c.2423T>G (p.Leu808Arg) c.899+32T>G c.2582T>G (p.Leu861Arg) c.*28+18903T>G (n.*28+18903T>G) c.2447T>G (p.Leu816Arg) c.1781T>G (p.Leu594Arg) | ClinVar dbSNP COSMIC |
| 7 | g.55191831T= | CA1708922660 | EGFR | c.2423T= (p.Leu808=) c.899+32T= c.2582T= (p.Leu861=) c.*28+18903T= (n.*28+18903T=) c.2447T= (p.Leu816=) c.1781T= (p.Leu594=) | |
| 7 | g.55191832G>A | CA454965654 | EGFR | c.2424G>A (p.Leu808=) c.899+33G>A c.2583G>A (p.Leu861=) c.*28+18904G>A (n.*28+18904G>A) c.2448G>A (p.Leu816=) c.1782G>A (p.Leu594=) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 7 | g.55191832G>C | CA454965655 | EGFR | c.2424G>C (p.Leu808=) c.899+33G>C c.2583G>C (p.Leu861=) c.*28+18904G>C (n.*28+18904G>C) c.2448G>C (p.Leu816=) c.1782G>C (p.Leu594=) | dbSNP gnomAD v4 |
| 7 | g.55191832G= | CA1708922671 | EGFR | c.2424G= (p.Leu808=) c.899+33G= c.2583G= (p.Leu861=) c.*28+18904G= (n.*28+18904G=) c.2448G= (p.Leu816=) c.1782G= (p.Leu594=) | |
| 7 | g.55191832G>T | CA454965656 | EGFR | c.2424G>T (p.Leu808=) c.899+33G>T c.2583G>T (p.Leu861=) c.*28+18904G>T (n.*28+18904G>T) c.2448G>T (p.Leu816=) c.1782G>T (p.Leu594=) | |
| 7 | g.55191833C>A | CA367580293 | EGFR | c.2425C>A (p.Leu809Met) c.899+34C>A c.2584C>A (p.Leu862Met) c.*28+18905C>A (n.*28+18905C>A) c.2449C>A (p.Leu817Met) c.1783C>A (p.Leu595Met) | dbSNP |
| 7 | g.55191833C>G | CA367580292 | EGFR | c.2425C>G (p.Leu809Val) c.899+34C>G c.2584C>G (p.Leu862Val) c.*28+18905C>G (n.*28+18905C>G) c.2449C>G (p.Leu817Val) c.1783C>G (p.Leu595Val) | |
| 7 | g.55191833C>T | CA454965657 | EGFR | c.2425C>T (p.Leu809=) c.899+34C>T c.2584C>T (p.Leu862=) c.*28+18905C>T (n.*28+18905C>T) c.2449C>T (p.Leu817=) c.1783C>T (p.Leu595=) | dbSNP gnomAD v4 |
| 7 | g.55191834T>A | CA367580294 | EGFR | c.2426T>A (p.Leu809Gln) c.899+35T>A c.2585T>A (p.Leu862Gln) c.*28+18906T>A (n.*28+18906T>A) c.2450T>A (p.Leu817Gln) c.1784T>A (p.Leu595Gln) | COSMIC |
| 7 | g.55191834T>C | CA367580295 | EGFR | c.2426T>C (p.Leu809Pro) c.899+35T>C c.2585T>C (p.Leu862Pro) c.*28+18906T>C (n.*28+18906T>C) c.2450T>C (p.Leu817Pro) c.1784T>C (p.Leu595Pro) | gnomAD v4 COSMIC |
| 7 | g.55191834T>G | CA367580296 | EGFR | c.2426T>G (p.Leu809Arg) c.899+35T>G c.2585T>G (p.Leu862Arg) c.*28+18906T>G (n.*28+18906T>G) c.2450T>G (p.Leu817Arg) c.1784T>G (p.Leu595Arg) | COSMIC |
| 7 | g.55191835G>A | CA454965658 | EGFR | c.2427G>A (p.Leu809=) c.899+36G>A c.2586G>A (p.Leu862=) c.*28+18907G>A (n.*28+18907G>A) c.2451G>A (p.Leu817=) c.1785G>A (p.Leu595=) | dbSNP gnomAD v4 |
| 7 | g.55191835G>C | CA454965659 | EGFR | c.2427G>C (p.Leu809=) c.899+36G>C c.2586G>C (p.Leu862=) c.*28+18907G>C (n.*28+18907G>C) c.2451G>C (p.Leu817=) c.1785G>C (p.Leu595=) | dbSNP |
| 7 | g.55191835G>T | CA454965660 | EGFR | c.2427G>T (p.Leu809=) c.899+36G>T c.2586G>T (p.Leu862=) c.*28+18907G>T (n.*28+18907G>T) c.2451G>T (p.Leu817=) c.1785G>T (p.Leu595=) | dbSNP |
| 7 | g.55191836G>A | CA367580297 | EGFR | c.2428G>A (p.Gly810Ser) c.899+37G>A c.2587G>A (p.Gly863Ser) c.*28+18908G>A (n.*28+18908G>A) c.2452G>A (p.Gly818Ser) c.1786G>A (p.Gly596Ser) | ClinVar dbSNP gnomAD v4 COSMIC |
| 7 | g.55191836G>C | CA367580298 | EGFR | c.2428G>C (p.Gly810Arg) c.899+37G>C c.2587G>C (p.Gly863Arg) c.*28+18908G>C (n.*28+18908G>C) c.2452G>C (p.Gly818Arg) c.1786G>C (p.Gly596Arg) | dbSNP |
| 7 | g.55191836G>T | CA367580299 | EGFR | c.2428G>T (p.Gly810Cys) c.899+37G>T c.2587G>T (p.Gly863Cys) c.*28+18908G>T (n.*28+18908G>T) c.2452G>T (p.Gly818Cys) c.1786G>T (p.Gly596Cys) | ClinVar dbSNP gnomAD v4 |
| 7 | g.55191837G>A | CA158934272 | EGFR | c.2429G>A (p.Gly810Asp) c.899+38G>A c.2588G>A (p.Gly863Asp) c.*28+18909G>A (n.*28+18909G>A) c.2453G>A (p.Gly818Asp) c.1787G>A (p.Gly596Asp) | ClinVar dbSNP gnomAD v4 COSMIC |
| 7 | g.55191837G>C | CA367580300 | EGFR | c.2429G>C (p.Gly810Ala) c.899+38G>C c.2588G>C (p.Gly863Ala) c.*28+18909G>C (n.*28+18909G>C) c.2453G>C (p.Gly818Ala) c.1787G>C (p.Gly596Ala) | dbSNP |
| 7 | g.55191837G= | CA1708922675 | EGFR | c.2429G= (p.Gly810=) c.899+38G= c.2588G= (p.Gly863=) c.*28+18909G= (n.*28+18909G=) c.2453G= (p.Gly818=) c.1787G= (p.Gly596=) | |
| 7 | g.55191837G>T | CA367580301 | EGFR | c.2429G>T (p.Gly810Val) c.899+38G>T c.2588G>T (p.Gly863Val) c.*28+18909G>T (n.*28+18909G>T) c.2453G>T (p.Gly818Val) c.1787G>T (p.Gly596Val) | COSMIC |
| 7 | g.55191838T>A | CA454965663 | EGFR | c.2430T>A (p.Gly810=) c.899+39T>A c.2589T>A (p.Gly863=) c.*28+18910T>A (n.*28+18910T>A) c.2454T>A (p.Gly818=) c.1788T>A (p.Gly596=) | dbSNP |
| 7 | g.55191838T>C | CA454965662 | EGFR | c.2430T>C (p.Gly810=) c.899+39T>C c.2589T>C (p.Gly863=) c.*28+18910T>C (n.*28+18910T>C) c.2454T>C (p.Gly818=) c.1788T>C (p.Gly596=) | |
| 7 | g.55191838T>G | CA454965661 | EGFR | c.2430T>G (p.Gly810=) c.899+39T>G c.2589T>G (p.Gly863=) c.*28+18910T>G (n.*28+18910T>G) c.2454T>G (p.Gly818=) c.1788T>G (p.Gly596=) | dbSNP COSMIC |
| 7 | g.55191839G>A | CA367580302 | EGFR | c.2431G>A (p.Ala811Thr) c.899+40G>A c.2590G>A (p.Ala864Thr) c.*28+18911G>A (n.*28+18911G>A) c.2455G>A (p.Ala819Thr) c.1789G>A (p.Ala597Thr) | ClinVar dbSNP gnomAD v4 COSMIC |
| 7 | g.55191839G>C | CA367580303 | EGFR | c.2431G>C (p.Ala811Pro) c.899+40G>C c.2590G>C (p.Ala864Pro) c.*28+18911G>C (n.*28+18911G>C) c.2455G>C (p.Ala819Pro) c.1789G>C (p.Ala597Pro) | dbSNP |
| 7 | g.55191839G= | CA1708922678 | EGFR | c.2431G= (p.Ala811=) c.899+40G= c.2590G= (p.Ala864=) c.*28+18911G= (n.*28+18911G=) c.2455G= (p.Ala819=) c.1789G= (p.Ala597=) | |
| 7 | g.55191839G>T | CA367580304 | EGFR | c.2431G>T (p.Ala811Ser) c.899+40G>T c.2590G>T (p.Ala864Ser) c.*28+18911G>T (n.*28+18911G>T) c.2455G>T (p.Ala819Ser) c.1789G>T (p.Ala597Ser) | dbSNP |
| 7 | g.55191840C>A | CA367580305 | EGFR | c.2432C>A (p.Ala811Glu) c.899+41C>A c.2591C>A (p.Ala864Glu) c.*28+18912C>A (n.*28+18912C>A) c.2456C>A (p.Ala819Glu) c.1790C>A (p.Ala597Glu) | dbSNP COSMIC |
| 7 | g.55191840C>G | CA367580306 | EGFR | c.2432C>G (p.Ala811Gly) c.899+41C>G c.2591C>G (p.Ala864Gly) c.*28+18912C>G (n.*28+18912C>G) c.2456C>G (p.Ala819Gly) c.1790C>G (p.Ala597Gly) | gnomAD v4 |
| 7 | g.55191840C>T | CA367580307 | EGFR | c.2432C>T (p.Ala811Val) c.899+41C>T c.2591C>T (p.Ala864Val) c.*28+18912C>T (n.*28+18912C>T) c.2456C>T (p.Ala819Val) c.1790C>T (p.Ala597Val) | ClinVar dbSNP gnomAD v4 COSMIC |
| 7 | g.55191841G>A | CA135943 | EGFR | c.2433G>A (p.Ala811=) c.899+42G>A c.2592G>A (p.Ala864=) c.*28+18913G>A (n.*28+18913G>A) c.2457G>A (p.Ala819=) c.1791G>A (p.Ala597=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 7 | g.55191841G>C | CA454965665 | EGFR | c.2433G>C (p.Ala811=) c.899+42G>C c.2592G>C (p.Ala864=) c.*28+18913G>C (n.*28+18913G>C) c.2457G>C (p.Ala819=) c.1791G>C (p.Ala597=) | dbSNP |
| 7 | g.55191841G= | CA1708922684 | EGFR | c.2433G= (p.Ala811=) c.899+42G= c.2592G= (p.Ala864=) c.*28+18913G= (n.*28+18913G=) c.2457G= (p.Ala819=) c.1791G= (p.Ala597=) | |
| 7 | g.55191841G>T | CA454965664 | EGFR | c.2433G>T (p.Ala811=) c.899+42G>T c.2592G>T (p.Ala864=) c.*28+18913G>T (n.*28+18913G>T) c.2457G>T (p.Ala819=) c.1791G>T (p.Ala597=) | dbSNP gnomAD v4 |
| 7 | g.55191842G>A | CA367580309 | EGFR | c.2434G>A (p.Glu812Lys) c.899+43G>A c.2593G>A (p.Glu865Lys) c.*28+18914G>A (n.*28+18914G>A) c.2458G>A (p.Glu820Lys) c.1792G>A (p.Glu598Lys) | ClinVar dbSNP gnomAD v4 COSMIC |
| 7 | g.55191842G>C | CA367580308 | EGFR | c.2434G>C (p.Glu812Gln) c.899+43G>C c.2593G>C (p.Glu865Gln) c.*28+18914G>C (n.*28+18914G>C) c.2458G>C (p.Glu820Gln) c.1792G>C (p.Glu598Gln) | dbSNP |
| 7 | g.55191842G>T | CA367580310 | EGFR | c.2434G>T (p.Glu812Ter) c.899+43G>T c.2593G>T (p.Glu865Ter) c.*28+18914G>T (n.*28+18914G>T) c.2458G>T (p.Glu820Ter) c.1792G>T (p.Glu598Ter) | |
| 7 | g.55191843A>C | CA367580311 | EGFR | c.2435A>C (p.Glu812Ala) c.899+44A>C c.2594A>C (p.Glu865Ala) c.*28+18915A>C (n.*28+18915A>C) c.2459A>C (p.Glu820Ala) c.1793A>C (p.Glu598Ala) | |
| 7 | g.55191843A>G | CA367580312 | EGFR | c.2435A>G (p.Glu812Gly) c.899+44A>G c.2594A>G (p.Glu865Gly) c.*28+18915A>G (n.*28+18915A>G) c.2459A>G (p.Glu820Gly) c.1793A>G (p.Glu598Gly) | dbSNP |
| 7 | g.55191843A>T | CA367580313 | EGFR | c.2435A>T (p.Glu812Val) c.899+44A>T c.2594A>T (p.Glu865Val) c.*28+18915A>T (n.*28+18915A>T) c.2459A>T (p.Glu820Val) c.1793A>T (p.Glu598Val) | dbSNP |
| 7 | g.55191844A>C | CA367580314 | EGFR | c.2436A>C (p.Glu812Asp) c.899+45A>C c.2595A>C (p.Glu865Asp) c.*28+18916A>C (n.*28+18916A>C) c.2460A>C (p.Glu820Asp) c.1794A>C (p.Glu598Asp) | |
| 7 | g.55191844A>G | CA454965666 | EGFR | c.2436A>G (p.Glu812=) c.899+45A>G c.2595A>G (p.Glu865=) c.*28+18916A>G (n.*28+18916A>G) c.2460A>G (p.Glu820=) c.1794A>G (p.Glu598=) | ClinVar dbSNP gnomAD v4 |
| 7 | g.55191844A>T | CA367580315 | EGFR | c.2436A>T (p.Glu812Asp) c.899+45A>T c.2595A>T (p.Glu865Asp) c.*28+18916A>T (n.*28+18916A>T) c.2460A>T (p.Glu820Asp) c.1794A>T (p.Glu598Asp) | dbSNP |
| 7 | g.55191845G>A | CA4266116 | EGFR | c.2437G>A (p.Glu813Lys) c.899+46G>A c.2596G>A (p.Glu866Lys) c.*28+18917G>A (n.*28+18917G>A) c.2461G>A (p.Glu821Lys) c.1795G>A (p.Glu599Lys) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC |
| 7 | g.55191845G>C | CA367580317 | EGFR | c.2437G>C (p.Glu813Gln) c.899+46G>C c.2596G>C (p.Glu866Gln) c.*28+18917G>C (n.*28+18917G>C) c.2461G>C (p.Glu821Gln) c.1795G>C (p.Glu599Gln) | COSMIC |
| 7 | g.55191845G= | CA1708922687 | EGFR | c.2437G= (p.Glu813=) c.899+46G= c.2596G= (p.Glu866=) c.*28+18917G= (n.*28+18917G=) c.2461G= (p.Glu821=) c.1795G= (p.Glu599=) | |
| 7 | g.55191845G>T | CA367580316 | EGFR | c.2437G>T (p.Glu813Ter) c.899+46G>T c.2596G>T (p.Glu866Ter) c.*28+18917G>T (n.*28+18917G>T) c.2461G>T (p.Glu821Ter) c.1795G>T (p.Glu599Ter) | |
| 7 | g.55191846A= | CA1708922693 | EGFR | c.2438A= (p.Glu813=) c.899+47A= c.2597A= (p.Glu866=) c.*28+18918A= (n.*28+18918A=) c.2462A= (p.Glu821=) c.1796A= (p.Glu599=) | |
| 7 | g.55191846A>C | CA367580318 | EGFR | c.2438A>C (p.Glu813Ala) c.899+47A>C c.2597A>C (p.Glu866Ala) c.*28+18918A>C (n.*28+18918A>C) c.2462A>C (p.Glu821Ala) c.1796A>C (p.Glu599Ala) | gnomAD v4 |
| 7 | g.55191846A>G | CA367580319 | EGFR | c.2438A>G (p.Glu813Gly) c.899+47A>G c.2597A>G (p.Glu866Gly) c.*28+18918A>G (n.*28+18918A>G) c.2462A>G (p.Glu821Gly) c.1796A>G (p.Glu599Gly) | dbSNP COSMIC |
| 7 | g.55191846A>T | CA135946 | EGFR | c.2438A>T (p.Glu813Val) c.899+47A>T c.2597A>T (p.Glu866Val) c.*28+18918A>T (n.*28+18918A>T) c.2462A>T (p.Glu821Val) c.1796A>T (p.Glu599Val) | ClinVar dbSNP COSMIC |
| 7 | g.55191847G>A | CA135949 | EGFR | c.2439G>A (p.Glu813=) c.899+48G>A c.2598G>A (p.Glu866=) c.*28+18919G>A (n.*28+18919G>A) c.2463G>A (p.Glu821=) c.1797G>A (p.Glu599=) | ClinVar dbSNP |
| 7 | g.55191847G>C | CA367580320 | EGFR | c.2439G>C (p.Glu813Asp) c.899+48G>C c.2598G>C (p.Glu866Asp) c.*28+18919G>C (n.*28+18919G>C) c.2463G>C (p.Glu821Asp) c.1797G>C (p.Glu599Asp) | dbSNP COSMIC |
| 7 | g.55191847G= | CA1708922700 | EGFR | c.2439G= (p.Glu813=) c.899+48G= c.2598G= (p.Glu866=) c.*28+18919G= (n.*28+18919G=) c.2463G= (p.Glu821=) c.1797G= (p.Glu599=) | |
| 7 | g.55191847G>T | CA367580321 | EGFR | c.2439G>T (p.Glu813Asp) c.899+48G>T c.2598G>T (p.Glu866Asp) c.*28+18919G>T (n.*28+18919G>T) c.2463G>T (p.Glu821Asp) c.1797G>T (p.Glu599Asp) | COSMIC |
| 7 | g.55191848A>C | CA367580322 | EGFR | c.2440A>C (p.Lys814Gln) c.899+49A>C c.2599A>C (p.Lys867Gln) c.*28+18920A>C (n.*28+18920A>C) c.2464A>C (p.Lys822Gln) c.1798A>C (p.Lys600Gln) | |
| 7 | g.55191848A>G | CA367580324 | EGFR | c.2440A>G (p.Lys814Glu) c.899+49A>G c.2599A>G (p.Lys867Glu) c.*28+18920A>G (n.*28+18920A>G) c.2464A>G (p.Lys822Glu) c.1798A>G (p.Lys600Glu) | dbSNP |
| 7 | g.55191848A>T | CA367580323 | EGFR | c.2440A>T (p.Lys814Ter) c.899+49A>T c.2599A>T (p.Lys867Ter) c.*28+18920A>T (n.*28+18920A>T) c.2464A>T (p.Lys822Ter) c.1798A>T (p.Lys600Ter) | |
| 7 | g.55191849A>C | CA367580325 | EGFR | c.2441A>C (p.Lys814Thr) c.899+50A>C c.2600A>C (p.Lys867Thr) c.*28+18921A>C (n.*28+18921A>C) c.2465A>C (p.Lys822Thr) c.1799A>C (p.Lys600Thr) | |
| 7 | g.55191849A>G | CA367580326 | EGFR | c.2441A>G (p.Lys814Arg) c.899+50A>G c.2600A>G (p.Lys867Arg) c.*28+18921A>G (n.*28+18921A>G) c.2465A>G (p.Lys822Arg) c.1799A>G (p.Lys600Arg) | dbSNP gnomAD v4 |
| 7 | g.55191849A>T | CA367580327 | EGFR | c.2441A>T (p.Lys814Ile) c.899+50A>T c.2600A>T (p.Lys867Ile) c.*28+18921A>T (n.*28+18921A>T) c.2465A>T (p.Lys822Ile) c.1799A>T (p.Lys600Ile) | |
| 7 | g.55191850A>C | CA367580328 | EGFR | c.2442A>C (p.Lys814Asn) c.899+51A>C c.2601A>C (p.Lys867Asn) c.*28+18922A>C (n.*28+18922A>C) c.2466A>C (p.Lys822Asn) c.1800A>C (p.Lys600Asn) | dbSNP |
| 7 | g.55191850A>G | CA454965667 | EGFR | c.2442A>G (p.Lys814=) c.899+51A>G c.2601A>G (p.Lys867=) c.*28+18922A>G (n.*28+18922A>G) c.2466A>G (p.Lys822=) c.1800A>G (p.Lys600=) | dbSNP |
| 7 | g.55191850A>T | CA367580329 | EGFR | c.2442A>T (p.Lys814Asn) c.899+51A>T c.2601A>T (p.Lys867Asn) c.*28+18922A>T (n.*28+18922A>T) c.2466A>T (p.Lys822Asn) c.1800A>T (p.Lys600Asn) | dbSNP |
| 7 | g.55191851G>A | CA269859 | EGFR | c.2443G>A (p.Glu815Lys) c.899+52G>A c.2602G>A (p.Glu868Lys) c.*28+18923G>A (n.*28+18923G>A) c.2467G>A (p.Glu823Lys) c.1801G>A (p.Glu601Lys) | ClinVar dbSNP gnomAD v3 gnomAD v4 COSMIC |
| 7 | g.55191851G>C | CA367580330 | EGFR | c.2443G>C (p.Glu815Gln) c.899+52G>C c.2602G>C (p.Glu868Gln) c.*28+18923G>C (n.*28+18923G>C) c.2467G>C (p.Glu823Gln) c.1801G>C (p.Glu601Gln) | dbSNP gnomAD v2 |
| 7 | g.55191851G= | CA1708922712 | EGFR | c.2443G= (p.Glu815=) c.899+52G= c.2602G= (p.Glu868=) c.*28+18923G= (n.*28+18923G=) c.2467G= (p.Glu823=) c.1801G= (p.Glu601=) | |
| 7 | g.55191851G>T | CA367580331 | EGFR | c.2443G>T (p.Glu815Ter) c.899+52G>T c.2602G>T (p.Glu868Ter) c.*28+18923G>T (n.*28+18923G>T) c.2467G>T (p.Glu823Ter) c.1801G>T (p.Glu601Ter) | |
| 7 | g.55191852A>C | CA367580332 | EGFR | c.2444A>C (p.Glu815Ala) c.899+53A>C c.2603A>C (p.Glu868Ala) c.*28+18924A>C (n.*28+18924A>C) c.2468A>C (p.Glu823Ala) c.1802A>C (p.Glu601Ala) | |
| 7 | g.55191852A>G | CA367580333 | EGFR | c.2444A>G (p.Glu815Gly) c.899+53A>G c.2603A>G (p.Glu868Gly) c.*28+18924A>G (n.*28+18924A>G) c.2468A>G (p.Glu823Gly) c.1802A>G (p.Glu601Gly) | dbSNP COSMIC |
| 7 | g.55191852A>T | CA367580334 | EGFR | c.2444A>T (p.Glu815Val) c.899+53A>T c.2603A>T (p.Glu868Val) c.*28+18924A>T (n.*28+18924A>T) c.2468A>T (p.Glu823Val) c.1802A>T (p.Glu601Val) | dbSNP COSMIC |
| 7 | g.55191853A>C | CA367580336 | EGFR | c.2445A>C (p.Glu815Asp) c.899+54A>C c.2604A>C (p.Glu868Asp) c.*28+18925A>C (n.*28+18925A>C) c.2469A>C (p.Glu823Asp) c.1803A>C (p.Glu601Asp) | dbSNP |
| 7 | g.55191853A>G | CA454965668 | EGFR | c.2445A>G (p.Glu815=) c.899+54A>G c.2604A>G (p.Glu868=) c.*28+18925A>G (n.*28+18925A>G) c.2469A>G (p.Glu823=) c.1803A>G (p.Glu601=) | ClinVar dbSNP gnomAD v4 |
| 7 | g.55191853A>T | CA367580335 | EGFR | c.2445A>T (p.Glu815Asp) c.899+54A>T c.2604A>T (p.Glu868Asp) c.*28+18925A>T (n.*28+18925A>T) c.2469A>T (p.Glu823Asp) c.1803A>T (p.Glu601Asp) | COSMIC |
| 7 | g.55191854T>A | CA367580337 | EGFR | c.2446T>A (p.Tyr816Asn) c.899+55T>A c.2605T>A (p.Tyr869Asn) c.*28+18926T>A (n.*28+18926T>A) c.2470T>A (p.Tyr824Asn) c.1804T>A (p.Tyr602Asn) | dbSNP |
| 7 | g.55191854T>C | CA367580338 | EGFR | c.2446T>C (p.Tyr816His) c.899+55T>C c.2605T>C (p.Tyr869His) c.*28+18926T>C (n.*28+18926T>C) c.2470T>C (p.Tyr824His) c.1804T>C (p.Tyr602His) | ClinVar |
| 7 | g.55191854T>G | CA367580339 | EGFR | c.2446T>G (p.Tyr816Asp) c.899+55T>G c.2605T>G (p.Tyr869Asp) c.*28+18926T>G (n.*28+18926T>G) c.2470T>G (p.Tyr824Asp) c.1804T>G (p.Tyr602Asp) | |
| 7 | g.55191855A= | CA1708922717 | EGFR | c.2447A= (p.Tyr816=) c.899+56A= c.2606A= (p.Tyr869=) c.*28+18927A= (n.*28+18927A=) c.2471A= (p.Tyr824=) c.1805A= (p.Tyr602=) | |
| 7 | g.55191855A>C | CA367580340 | EGFR | c.2447A>C (p.Tyr816Ser) c.899+56A>C c.2606A>C (p.Tyr869Ser) c.*28+18927A>C (n.*28+18927A>C) c.2471A>C (p.Tyr824Ser) c.1805A>C (p.Tyr602Ser) | |
| 7 | g.55191855A>G | CA367580341 | EGFR | c.2447A>G (p.Tyr816Cys) c.899+56A>G c.2606A>G (p.Tyr869Cys) c.*28+18927A>G (n.*28+18927A>G) c.2471A>G (p.Tyr824Cys) c.1805A>G (p.Tyr602Cys) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 7 | g.55191855A>T | CA367580342 | EGFR | c.2447A>T (p.Tyr816Phe) c.899+56A>T c.2606A>T (p.Tyr869Phe) c.*28+18927A>T (n.*28+18927A>T) c.2471A>T (p.Tyr824Phe) c.1805A>T (p.Tyr602Phe) | |
| 7 | g.55191856C>A | CA367580343 | EGFR | c.2448C>A (p.Tyr816Ter) c.899+57C>A c.2607C>A (p.Tyr869Ter) c.*28+18928C>A (n.*28+18928C>A) c.2472C>A (p.Tyr824Ter) c.1806C>A (p.Tyr602Ter) | |
| 7 | g.55191856C>G | CA367580344 | EGFR | c.2448C>G (p.Tyr816Ter) c.899+57C>G c.2607C>G (p.Tyr869Ter) c.*28+18928C>G (n.*28+18928C>G) c.2472C>G (p.Tyr824Ter) c.1806C>G (p.Tyr602Ter) | |
| 7 | g.55191856C>T | CA454965669 | EGFR | c.2448C>T (p.Tyr816=) c.899+57C>T c.2607C>T (p.Tyr869=) c.*28+18928C>T (n.*28+18928C>T) c.2472C>T (p.Tyr824=) c.1806C>T (p.Tyr602=) | ClinVar dbSNP |
| 7 | g.55191857C>A | CA367580345 | EGFR | c.2449C>A (p.His817Asn) c.899+58C>A c.2608C>A (p.His870Asn) c.*28+18929C>A (n.*28+18929C>A) c.2473C>A (p.His825Asn) c.1807C>A (p.His603Asn) | dbSNP |
| 7 | g.55191857C>G | CA367580346 | EGFR | c.2449C>G (p.His817Asp) c.899+58C>G c.2608C>G (p.His870Asp) c.*28+18929C>G (n.*28+18929C>G) c.2473C>G (p.His825Asp) c.1807C>G (p.His603Asp) | dbSNP |
| 7 | g.55191857C>T | CA367580347 | EGFR | c.2449C>T (p.His817Tyr) c.899+58C>T c.2608C>T (p.His870Tyr) c.*28+18929C>T (n.*28+18929C>T) c.2473C>T (p.His825Tyr) c.1807C>T (p.His603Tyr) | dbSNP COSMIC |
| 7 | g.55191858A= | CA1708922720 | EGFR | c.2450A= (p.His817=) c.899+59A= c.2609A= (p.His870=) c.*28+18930A= (n.*28+18930A=) c.2474A= (p.His825=) c.1808A= (p.His603=) | |
| 7 | g.55191858A>C | CA367580348 | EGFR | c.2450A>C (p.His817Pro) c.899+59A>C c.2609A>C (p.His870Pro) c.*28+18930A>C (n.*28+18930A>C) c.2474A>C (p.His825Pro) c.1808A>C (p.His603Pro) | dbSNP |
| 7 | g.55191858A>G | CA367580349 | EGFR | c.2450A>G (p.His817Arg) c.899+59A>G c.2609A>G (p.His870Arg) c.*28+18930A>G (n.*28+18930A>G) c.2474A>G (p.His825Arg) c.1808A>G (p.His603Arg) | ClinVar dbSNP COSMIC |
| 7 | g.55191858A>T | CA367580350 | EGFR | c.2450A>T (p.His817Leu) c.899+59A>T c.2609A>T (p.His870Leu) c.*28+18930A>T (n.*28+18930A>T) c.2474A>T (p.His825Leu) c.1808A>T (p.His603Leu) | dbSNP |
| 7 | g.55191859T>A | CA367580352 | EGFR | c.2451T>A (p.His817Gln) c.899+60T>A c.2610T>A (p.His870Gln) c.*28+18931T>A (n.*28+18931T>A) c.2475T>A (p.His825Gln) c.1809T>A (p.His603Gln) | |
| 7 | g.55191859T>C | CA454965670 | EGFR | c.2451T>C (p.His817=) c.899+60T>C c.2610T>C (p.His870=) c.*28+18931T>C (n.*28+18931T>C) c.2475T>C (p.His825=) c.1809T>C (p.His603=) | ClinVar dbSNP gnomAD v4 |
| 7 | g.55191859T>G | CA367580351 | EGFR | c.2451T>G (p.His817Gln) c.899+60T>G c.2610T>G (p.His870Gln) c.*28+18931T>G (n.*28+18931T>G) c.2475T>G (p.His825Gln) c.1809T>G (p.His603Gln) | |
| 7 | g.55191859T= | CA1708922723 | EGFR | c.2451T= (p.His817=) c.899+60T= c.2610T= (p.His870=) c.*28+18931T= (n.*28+18931T=) c.2475T= (p.His825=) c.1809T= (p.His603=) | |
| 7 | g.55191860G>A | CA367580353 | EGFR | c.2452G>A (p.Ala818Thr) c.899+61G>A c.2611G>A (p.Ala871Thr) c.*28+18932G>A (n.*28+18932G>A) c.2476G>A (p.Ala826Thr) c.1810G>A (p.Ala604Thr) | dbSNP COSMIC |
| 7 | g.55191860G>C | CA367580354 | EGFR | c.2452G>C (p.Ala818Pro) c.899+61G>C c.2611G>C (p.Ala871Pro) c.*28+18932G>C (n.*28+18932G>C) c.2476G>C (p.Ala826Pro) c.1810G>C (p.Ala604Pro) | dbSNP |
| 7 | g.55191860G>T | CA367580355 | EGFR | c.2452G>T (p.Ala818Ser) c.899+61G>T c.2611G>T (p.Ala871Ser) c.*28+18932G>T (n.*28+18932G>T) c.2476G>T (p.Ala826Ser) c.1810G>T (p.Ala604Ser) | |
| 7 | g.55191861C>A | CA367580356 | EGFR | c.2453C>A (p.Ala818Glu) c.899+62C>A c.2612C>A (p.Ala871Glu) c.*28+18933C>A (n.*28+18933C>A) c.2477C>A (p.Ala826Glu) c.1811C>A (p.Ala604Glu) | dbSNP |
| 7 | g.55191861C= | CA1708922729 | EGFR | c.2453C= (p.Ala818=) c.899+62C= c.2612C= (p.Ala871=) c.*28+18933C= (n.*28+18933C=) c.2477C= (p.Ala826=) c.1811C= (p.Ala604=) | |
| 7 | g.55191861C>G | CA135952 | EGFR | c.2453C>G (p.Ala818Gly) c.899+62C>G c.2612C>G (p.Ala871Gly) c.*28+18933C>G (n.*28+18933C>G) c.2477C>G (p.Ala826Gly) c.1811C>G (p.Ala604Gly) | ClinVar dbSNP COSMIC |
| 7 | g.55191861C>T | CA367580357 | EGFR | c.2453C>T (p.Ala818Val) c.899+62C>T c.2612C>T (p.Ala871Val) c.*28+18933C>T (n.*28+18933C>T) c.2477C>T (p.Ala826Val) c.1811C>T (p.Ala604Val) | dbSNP COSMIC |
| 7 | g.55191862A>C | CA454965671 | EGFR | c.2454A>C (p.Ala818=) c.899+63A>C c.2613A>C (p.Ala871=) c.*28+18934A>C (n.*28+18934A>C) c.2478A>C (p.Ala826=) c.1812A>C (p.Ala604=) | |
| 7 | g.55191862A>G | CA454965673 | EGFR | c.2454A>G (p.Ala818=) c.899+63A>G c.2613A>G (p.Ala871=) c.*28+18934A>G (n.*28+18934A>G) c.2478A>G (p.Ala826=) c.1812A>G (p.Ala604=) | ClinVar dbSNP gnomAD v4 |
| 7 | g.55191862A>T | CA454965672 | EGFR | c.2454A>T (p.Ala818=) c.899+63A>T c.2613A>T (p.Ala871=) c.*28+18934A>T (n.*28+18934A>T) c.2478A>T (p.Ala826=) c.1812A>T (p.Ala604=) | dbSNP |
| 7 | g.55191864_55191866del | CA2573142251 | EGFR | c.2456_2458del (p.Glu819del) c.899+65_899+67del c.2615_2617del (p.Glu872del) c.*28+18936_*28+18938del (n.*28+18936_*28+18938del) c.2480_2482del (p.Glu827del) c.1814_1816del (p.Glu605del) | ClinVar dbSNP |
| 7 | g.55191863G>A | CA367580360 | EGFR | c.2455G>A (p.Glu819Lys) c.899+64G>A c.2614G>A (p.Glu872Lys) c.*28+18935G>A (n.*28+18935G>A) c.2479G>A (p.Glu827Lys) c.1813G>A (p.Glu605Lys) | COSMIC |
| 7 | g.55191863G>C | CA367580358 | EGFR | c.2455G>C (p.Glu819Gln) c.899+64G>C c.2614G>C (p.Glu872Gln) c.*28+18935G>C (n.*28+18935G>C) c.2479G>C (p.Glu827Gln) c.1813G>C (p.Glu605Gln) | ClinVar dbSNP |
| 7 | g.55191863G>T | CA367580359 | EGFR | c.2455G>T (p.Glu819Ter) c.899+64G>T c.2614G>T (p.Glu872Ter) c.*28+18935G>T (n.*28+18935G>T) c.2479G>T (p.Glu827Ter) c.1813G>T (p.Glu605Ter) | COSMIC |
| 7 | g.55191864A>C | CA367580361 | EGFR | c.2456A>C (p.Glu819Ala) c.899+65A>C c.2615A>C (p.Glu872Ala) c.*28+18936A>C (n.*28+18936A>C) c.2480A>C (p.Glu827Ala) c.1814A>C (p.Glu605Ala) | |
| 7 | g.55191864A>G | CA367580362 | EGFR | c.2456A>G (p.Glu819Gly) c.899+65A>G c.2615A>G (p.Glu872Gly) c.*28+18936A>G (n.*28+18936A>G) c.2480A>G (p.Glu827Gly) c.1814A>G (p.Glu605Gly) | COSMIC |
| 7 | g.55191864A>T | CA367580363 | EGFR | c.2456A>T (p.Glu819Val) c.899+65A>T c.2615A>T (p.Glu872Val) c.*28+18936A>T (n.*28+18936A>T) c.2480A>T (p.Glu827Val) c.1814A>T (p.Glu605Val) | |
| 7 | g.55191865A>C | CA367580364 | EGFR | c.2457A>C (p.Glu819Asp) c.899+66A>C c.2616A>C (p.Glu872Asp) c.*28+18937A>C (n.*28+18937A>C) c.2481A>C (p.Glu827Asp) c.1815A>C (p.Glu605Asp) | |
| 7 | g.55191865A>G | CA454965674 | EGFR | c.2457A>G (p.Glu819=) c.899+66A>G c.2616A>G (p.Glu872=) c.*28+18937A>G (n.*28+18937A>G) c.2481A>G (p.Glu827=) c.1815A>G (p.Glu605=) | dbSNP |
| 7 | g.55191865A>T | CA367580365 | EGFR | c.2457A>T (p.Glu819Asp) c.899+66A>T c.2616A>T (p.Glu872Asp) c.*28+18937A>T (n.*28+18937A>T) c.2481A>T (p.Glu827Asp) c.1815A>T (p.Glu605Asp) | dbSNP |
| 7 | g.55191866G>A | CA367580366 | EGFR | c.2458G>A (p.Gly820Arg) c.899+67G>A c.2617G>A (p.Gly873Arg) c.*28+18938G>A (n.*28+18938G>A) c.2482G>A (p.Gly828Arg) c.1816G>A (p.Gly606Arg) | dbSNP gnomAD v4 |
| 7 | g.55191866G>C | CA367580368 | EGFR | c.2458G>C (p.Gly820Arg) c.899+67G>C c.2617G>C (p.Gly873Arg) c.*28+18938G>C (n.*28+18938G>C) c.2482G>C (p.Gly828Arg) c.1816G>C (p.Gly606Arg) | |
| 7 | g.55191866G>T | CA367580367 | EGFR | c.2458G>T (p.Gly820Ter) c.899+67G>T c.2617G>T (p.Gly873Ter) c.*28+18938G>T (n.*28+18938G>T) c.2482G>T (p.Gly828Ter) c.1816G>T (p.Gly606Ter) | dbSNP |
| 7 | g.55191867G>A | CA367580369 | EGFR | c.2459G>A (p.Gly820Glu) c.899+68G>A c.2618G>A (p.Gly873Glu) c.*28+18939G>A (n.*28+18939G>A) c.2483G>A (p.Gly828Glu) c.1817G>A (p.Gly606Glu) | ClinVar dbSNP gnomAD v4 COSMIC |
| 7 | g.55191867G>C | CA367580371 | EGFR | c.2459G>C (p.Gly820Ala) c.899+68G>C c.2618G>C (p.Gly873Ala) c.*28+18939G>C (n.*28+18939G>C) c.2483G>C (p.Gly828Ala) c.1817G>C (p.Gly606Ala) | dbSNP |
| 7 | g.55191867G>T | CA367580370 | EGFR | c.2459G>T (p.Gly820Val) c.899+68G>T c.2618G>T (p.Gly873Val) c.*28+18939G>T (n.*28+18939G>T) c.2483G>T (p.Gly828Val) c.1817G>T (p.Gly606Val) | gnomAD v4 |
| 7 | g.55191868A= | CA1708922734 | EGFR | c.2460A= (p.Gly820=) c.899+69A= c.2619A= (p.Gly873=) c.*28+18940A= (n.*28+18940A=) c.2484A= (p.Gly828=) c.1818A= (p.Gly606=) | |
| 7 | g.55191868A>C | CA454965675 | EGFR | c.2460A>C (p.Gly820=) c.899+69A>C c.2619A>C (p.Gly873=) c.*28+18940A>C (n.*28+18940A>C) c.2484A>C (p.Gly828=) c.1818A>C (p.Gly606=) | |
| 7 | g.55191868A>G | CA454965676 | EGFR | c.2460A>G (p.Gly820=) c.899+69A>G c.2619A>G (p.Gly873=) c.*28+18940A>G (n.*28+18940A>G) c.2484A>G (p.Gly828=) c.1818A>G (p.Gly606=) | dbSNP |
| 7 | g.55191868A>T | CA4266117 | EGFR | c.2460A>T (p.Gly820=) c.899+69A>T c.2619A>T (p.Gly873=) c.*28+18940A>T (n.*28+18940A>T) c.2484A>T (p.Gly828=) c.1818A>T (p.Gly606=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC |
| 7 | g.55191869G>A | CA367580372 | EGFR | c.2461G>A (p.Gly821Ser) c.899+70G>A c.2620G>A (p.Gly874Ser) c.*28+18941G>A (n.*28+18941G>A) c.2485G>A (p.Gly829Ser) c.1819G>A (p.Gly607Ser) | dbSNP COSMIC |
| 7 | g.55191869G>C | CA367580373 | EGFR | c.2461G>C (p.Gly821Arg) c.899+70G>C c.2620G>C (p.Gly874Arg) c.*28+18941G>C (n.*28+18941G>C) c.2485G>C (p.Gly829Arg) c.1819G>C (p.Gly607Arg) | dbSNP |
| 7 | g.55191869G>T | CA367580374 | EGFR | c.2461G>T (p.Gly821Cys) c.899+70G>T c.2620G>T (p.Gly874Cys) c.*28+18941G>T (n.*28+18941G>T) c.2485G>T (p.Gly829Cys) c.1819G>T (p.Gly607Cys) | |
| 7 | g.55191870G>A | CA367580375 | EGFR | c.2462G>A (p.Gly821Asp) c.899+71G>A c.2621G>A (p.Gly874Asp) c.*28+18942G>A (n.*28+18942G>A) c.2486G>A (p.Gly829Asp) c.1820G>A (p.Gly607Asp) | dbSNP |
| 7 | g.55191870G>C | CA367580376 | EGFR | c.2462G>C (p.Gly821Ala) c.899+71G>C c.2621G>C (p.Gly874Ala) c.*28+18942G>C (n.*28+18942G>C) c.2486G>C (p.Gly829Ala) c.1820G>C (p.Gly607Ala) | dbSNP |
| 7 | g.55191870G= | CA1708922738 | EGFR | c.2462G= (p.Gly821=) c.899+71G= c.2621G= (p.Gly874=) c.*28+18942G= (n.*28+18942G=) c.2486G= (p.Gly829=) c.1820G= (p.Gly607=) | |
| 7 | g.55191870G>T | CA367580377 | EGFR | c.2462G>T (p.Gly821Val) c.899+71G>T c.2621G>T (p.Gly874Val) c.*28+18942G>T (n.*28+18942G>T) c.2486G>T (p.Gly829Val) c.1820G>T (p.Gly607Val) | dbSNP |