SUSPENSION NOTICE:2024-08-07T19:00:00-0500 — 2024-09-25T08:00:00-0500
New user registrations, changes to existing user profiles, and changes to user credentials will be suspended for several weeks.
This allows us to avoid multi-day, broad service outages as we continue to migrate off our current cloud hosting provider.
New user registrations, changes to existing user profiles, and changes to user credentials will be suspended for several weeks.
This allows us to avoid multi-day, broad service outages as we continue to migrate off our current cloud hosting provider.
| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 7 | g.55151258_55151275del | CA2714929928 | EGFR | c.401-36_401-19del (n.401-36_401-19del) n.750-36_750-19del c.560-36_560-19del (n.560-36_560-19del) c.425-36_425-19del (n.425-36_425-19del) c.89-4572_89-4555del (n.89-4572_89-4555del) | dbSNP |
| 7 | g.55151273T>A | CA4265262 | EGFR | c.401-21T>A (n.401-21T>A) n.750-21T>A c.560-21T>A (n.560-21T>A) c.425-21T>A (n.425-21T>A) c.89-4557T>A (n.89-4557T>A) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 7 | g.55151273T= | CA1708910278 | EGFR | c.401-21T= (n.401-21T=) n.750-21T= c.560-21T= (n.560-21T=) c.425-21T= (n.425-21T=) c.89-4557T= (n.89-4557T=) | |
| 7 | g.55151274C>G | CA2714930389 | EGFR | c.401-20C>G (n.401-20C>G) n.750-20C>G c.560-20C>G (n.560-20C>G) c.425-20C>G (n.425-20C>G) c.89-4556C>G (n.89-4556C>G) | dbSNP |
| 7 | g.55151274C>T | CA2573142252 | EGFR | c.401-20C>T (n.401-20C>T) n.750-20C>T c.560-20C>T (n.560-20C>T) c.425-20C>T (n.425-20C>T) c.89-4556C>T (n.89-4556C>T) | ClinVar dbSNP |
| 7 | g.55151275T>A | CA1708910283 | EGFR | c.401-19T>A (n.401-19T>A) n.750-19T>A c.560-19T>A (n.560-19T>A) c.425-19T>A (n.425-19T>A) c.89-4555T>A (n.89-4555T>A) | dbSNP |
| 7 | g.55151275T>C | CA1708910284 | EGFR | c.401-19T>C (n.401-19T>C) n.750-19T>C c.560-19T>C (n.560-19T>C) c.425-19T>C (n.425-19T>C) c.89-4555T>C (n.89-4555T>C) | ClinVar dbSNP |
| 7 | g.55151275T= | CA1708910282 | EGFR | c.401-19T= (n.401-19T=) n.750-19T= c.560-19T= (n.560-19T=) c.425-19T= (n.425-19T=) c.89-4555T= (n.89-4555T=) | |
| 7 | g.55151276A>T | CA2714930390 | EGFR | c.401-18A>T (n.401-18A>T) n.750-18A>T c.560-18A>T (n.560-18A>T) c.425-18A>T (n.425-18A>T) c.89-4554A>T (n.89-4554A>T) | dbSNP |
| 7 | g.55151276_55151282delinsATTACTT | CA1708910287 | EGFR | c.401-18_401-12delinsATTACTT (n.401-18_401-12delinsATTACTT) n.750-18_750-12delinsATTACTT c.560-18_560-12delinsATTACTT (n.560-18_560-12delinsATTACTT) c.425-18_425-12delinsATTACTT (n.425-18_425-12delinsATTACTT) c.89-4554_89-4548delinsATTACTT (n.89-4554_89-4548delinsATTACTT) | |
| 7 | g.55151277T>C | CA2573142253 | EGFR | c.401-17T>C (n.401-17T>C) n.750-17T>C c.560-17T>C (n.560-17T>C) c.425-17T>C (n.425-17T>C) c.89-4553T>C (n.89-4553T>C) | ClinVar dbSNP gnomAD v4 |
| 7 | g.55151277T>G | CA2682851566 | EGFR | c.401-17T>G (n.401-17T>G) n.750-17T>G c.560-17T>G (n.560-17T>G) c.425-17T>G (n.425-17T>G) c.89-4553T>G (n.89-4553T>G) | ClinVar gnomAD v4 |
| 7 | g.55151281_55151286del | CA4265263 | EGFR | c.401-13_401-8del (n.401-13_401-8del) n.750-13_750-8del c.560-13_560-8del (n.560-13_560-8del) c.425-13_425-8del (n.425-13_425-8del) c.89-4549_89-4544del (n.89-4549_89-4544del) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 7 | g.55151278T>A | CA2682851567 | EGFR | c.401-16T>A (n.401-16T>A) n.750-16T>A c.560-16T>A (n.560-16T>A) c.425-16T>A (n.425-16T>A) c.89-4552T>A (n.89-4552T>A) | gnomAD v4 |
| 7 | g.55151279A= | CA1708910290 | EGFR | c.401-15A= (n.401-15A=) n.750-15A= c.560-15A= (n.560-15A=) c.425-15A= (n.425-15A=) c.89-4551A= (n.89-4551A=) | |
| 7 | g.55151279A>G | CA158909400 | EGFR | c.401-15A>G (n.401-15A>G) n.750-15A>G c.560-15A>G (n.560-15A>G) c.425-15A>G (n.425-15A>G) c.89-4551A>G (n.89-4551A>G) | ClinVar dbSNP |
| 7 | g.55151279A>T | CA2714508298 | EGFR | c.401-15A>T (n.401-15A>T) n.750-15A>T c.560-15A>T (n.560-15A>T) c.425-15A>T (n.425-15A>T) c.89-4551A>T (n.89-4551A>T) | dbSNP |
| 7 | g.55151281T>A | CA2714930435 | EGFR | c.401-13T>A (n.401-13T>A) n.750-13T>A c.560-13T>A (n.560-13T>A) c.425-13T>A (n.425-13T>A) c.89-4549T>A (n.89-4549T>A) | dbSNP |
| 7 | g.55151281T>G | CA2578642750 | EGFR | c.401-13T>G (n.401-13T>G) n.750-13T>G c.560-13T>G (n.560-13T>G) c.425-13T>G (n.425-13T>G) c.89-4549T>G (n.89-4549T>G) | |
| 7 | g.55151282T>A | CA2714930464 | EGFR | c.401-12T>A (n.401-12T>A) n.750-12T>A c.560-12T>A (n.560-12T>A) c.425-12T>A (n.425-12T>A) c.89-4548T>A (n.89-4548T>A) | dbSNP |
| 7 | g.55151282T>C | CA2682851568 | EGFR | c.401-12T>C (n.401-12T>C) n.750-12T>C c.560-12T>C (n.560-12T>C) c.425-12T>C (n.425-12T>C) c.89-4548T>C (n.89-4548T>C) | gnomAD v4 |
| 7 | g.55151284T>C | CA2573142254 | EGFR | c.401-10T>C (n.401-10T>C) n.750-10T>C c.560-10T>C (n.560-10T>C) c.425-10T>C (n.425-10T>C) c.89-4546T>C (n.89-4546T>C) | ClinVar dbSNP gnomAD v4 |
| 7 | g.55151285A= | CA1708910294 | EGFR | c.401-9A= (n.401-9A=) n.750-9A= c.560-9A= (n.560-9A=) c.425-9A= (n.425-9A=) c.89-4545A= (n.89-4545A=) | |
| 7 | g.55151285A>G | CA4265264 | EGFR | c.401-9A>G (n.401-9A>G) n.750-9A>G c.560-9A>G (n.560-9A>G) c.425-9A>G (n.425-9A>G) c.89-4545A>G (n.89-4545A>G) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 7 | g.55151285A>T | CA2714512712 | EGFR | c.401-9A>T (n.401-9A>T) n.750-9A>T c.560-9A>T (n.560-9A>T) c.425-9A>T (n.425-9A>T) c.89-4545A>T (n.89-4545A>T) | dbSNP |
| 7 | g.55151286del | CA2499218910 | EGFR | c.401-8del (n.401-8del) n.750-8del c.560-8del (n.560-8del) c.425-8del (n.425-8del) c.89-4544del (n.89-4544del) | ClinVar dbSNP |
| 7 | g.55151286C>G | CA2714930480 | EGFR | c.401-8C>G (n.401-8C>G) n.750-8C>G c.560-8C>G (n.560-8C>G) c.425-8C>G (n.425-8C>G) c.89-4544C>G (n.89-4544C>G) | dbSNP |
| 7 | g.55151286C>T | CA2580077233 | EGFR | c.401-8C>T (n.401-8C>T) n.750-8C>T c.560-8C>T (n.560-8C>T) c.425-8C>T (n.425-8C>T) c.89-4544C>T (n.89-4544C>T) | ClinVar dbSNP |
| 7 | g.55151287A>G | CA2578642751 | EGFR | c.401-7A>G (n.401-7A>G) n.750-7A>G c.560-7A>G (n.560-7A>G) c.425-7A>G (n.425-7A>G) c.89-4543A>G (n.89-4543A>G) | |
| 7 | g.55151287A>T | CA2714931019 | EGFR | c.401-7A>T (n.401-7A>T) n.750-7A>T c.560-7A>T (n.560-7A>T) c.425-7A>T (n.425-7A>T) c.89-4543A>T (n.89-4543A>T) | dbSNP |
| 7 | g.55151288T>C | CA574329148 | EGFR | c.401-6T>C (n.401-6T>C) n.750-6T>C c.560-6T>C (n.560-6T>C) c.425-6T>C (n.425-6T>C) c.89-4542T>C (n.89-4542T>C) | dbSNP gnomAD v2 gnomAD v4 |
| 7 | g.55151288T= | CA1708910297 | EGFR | c.401-6T= (n.401-6T=) n.750-6T= c.560-6T= (n.560-6T=) c.425-6T= (n.425-6T=) c.89-4542T= (n.89-4542T=) | |
| 7 | g.55151290dup | CA2840245956 | EGFR | c.401-4dup (n.401-4dup) n.750-4dup c.560-4dup (n.560-4dup) c.425-4dup (n.425-4dup) c.89-4540dup (n.89-4540dup) | |
| 7 | g.55151291C>A | CA2714931104 | EGFR | c.401-3C>A (n.401-3C>A) n.750-3C>A c.560-3C>A (n.560-3C>A) c.425-3C>A (n.425-3C>A) c.89-4539C>A (n.89-4539C>A) | dbSNP |
| 7 | g.55151291C>G | CA2714931057 | EGFR | c.401-3C>G (n.401-3C>G) n.750-3C>G c.560-3C>G (n.560-3C>G) c.425-3C>G (n.425-3C>G) c.89-4539C>G (n.89-4539C>G) | dbSNP |
| 7 | g.55151291C>T | CA2569033719 | EGFR | c.401-3C>T (n.401-3C>T) n.750-3C>T c.560-3C>T (n.560-3C>T) c.425-3C>T (n.425-3C>T) c.89-4539C>T (n.89-4539C>T) | dbSNP |
| 7 | g.55151291_55151299delinsCAGGCCAAA | CA1708910298 | EGFR | c.401-3_406delinsCAGGCCAAA n.750-3_755delinsCAGGCCAAA c.560-3_565delinsCAGGCCAAA c.425-3_430delinsCAGGCCAAA c.89-4539_89-4531delinsCAGGCCAAA (n.89-4539_89-4531delinsCAGGCCAAA) | |
| 7 | g.55151292A>C | CA367576770 | EGFR | c.401-2A>C (n.401-2A>C) n.750-2A>C c.560-2A>C (n.560-2A>C) c.425-2A>C (n.425-2A>C) c.89-4538A>C (n.89-4538A>C) | |
| 7 | g.55151292A>G | CA367576771 | EGFR | c.401-2A>G (n.401-2A>G) n.750-2A>G c.560-2A>G (n.560-2A>G) c.425-2A>G (n.425-2A>G) c.89-4538A>G (n.89-4538A>G) | dbSNP |
| 7 | g.55151292A>T | CA367576772 | EGFR | c.401-2A>T (n.401-2A>T) n.750-2A>T c.560-2A>T (n.560-2A>T) c.425-2A>T (n.425-2A>T) c.89-4538A>T (n.89-4538A>T) | dbSNP |
| 7 | g.55151294_55151301del | CA454963228 | EGFR | c.401_408del n.750_757del c.560_567del c.425_432del c.89-4536_89-4529del (n.89-4536_89-4529del) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 7 | g.55151293G>A | CA367576775 | EGFR | c.401-1G>A (n.401-1G>A) n.750-1G>A c.560-1G>A (n.560-1G>A) c.425-1G>A (n.425-1G>A) c.89-4537G>A (n.89-4537G>A) | dbSNP |
| 7 | g.55151293G>C | CA367576774 | EGFR | c.401-1G>C (n.401-1G>C) n.750-1G>C c.560-1G>C (n.560-1G>C) c.425-1G>C (n.425-1G>C) c.89-4537G>C (n.89-4537G>C) | dbSNP |
| 7 | g.55151293G>T | CA367576773 | EGFR | c.401-1G>T (n.401-1G>T) n.750-1G>T c.560-1G>T (n.560-1G>T) c.425-1G>T (n.425-1G>T) c.89-4537G>T (n.89-4537G>T) | dbSNP |
| 7 | g.55151294G>A | CA367576776 | EGFR | c.401G>A (p.Cys134Tyr) n.750G>A c.560G>A (p.Cys187Tyr) c.425G>A (p.Gly142Asp) c.89-4536G>A (n.89-4536G>A) | dbSNP |
| 7 | g.55151294G>C | CA367576778 | EGFR | c.401G>C (p.Cys134Ser) n.750G>C c.560G>C (p.Cys187Ser) c.425G>C (p.Gly142Ala) c.89-4536G>C (n.89-4536G>C) | dbSNP |
| 7 | g.55151294G>T | CA367576777 | EGFR | c.401G>T (p.Cys134Phe) n.750G>T c.560G>T (p.Cys187Phe) c.425G>T (p.Gly142Val) c.89-4536G>T (n.89-4536G>T) | dbSNP |
| 7 | g.55151295C>A | CA367576779 | EGFR | c.402C>A (p.Cys134Ter) n.751C>A c.561C>A (p.Cys187Ter) c.426C>A (p.Gly142=) c.89-4535C>A (n.89-4535C>A) | dbSNP |
| 7 | g.55151295C= | CA1708910304 | EGFR | c.402C= (p.Cys134=) n.751C= c.561C= (p.Cys187=) c.426C= (p.Gly142=) c.89-4535C= (n.89-4535C=) | |
| 7 | g.55151295C>G | CA367576780 | EGFR | c.402C>G (p.Cys134Trp) n.751C>G c.561C>G (p.Cys187Trp) c.426C>G (p.Gly142=) c.89-4535C>G (n.89-4535C>G) | dbSNP |
| 7 | g.55151295C>T | CA4265265 | EGFR | c.402C>T (p.Cys134=) n.751C>T c.561C>T (p.Cys187=) c.426C>T (p.Gly142=) c.89-4535C>T (n.89-4535C>T) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC COSMIC COSMIC COSMIC |
| 7 | g.55151296C>A | CA367576781 | EGFR | c.403C>A (p.Gln135Lys) n.752C>A c.562C>A (p.Gln188Lys) c.427C>A (p.Gln143Lys) c.89-4534C>A (n.89-4534C>A) | dbSNP |
| 7 | g.55151296C>G | CA367576783 | EGFR | c.403C>G (p.Gln135Glu) n.752C>G c.562C>G (p.Gln188Glu) c.427C>G (p.Gln143Glu) c.89-4534C>G (n.89-4534C>G) | dbSNP |
| 7 | g.55151296C>T | CA367576782 | EGFR | c.403C>T (p.Gln135Ter) n.752C>T c.562C>T (p.Gln188Ter) c.427C>T (p.Gln143Ter) c.89-4534C>T (n.89-4534C>T) | |
| 7 | g.55151297A= | CA1708910307 | EGFR | c.404A= (p.Gln135=) n.753A= c.563A= (p.Gln188=) c.428A= (p.Gln143=) c.89-4533A= (n.89-4533A=) | |
| 7 | g.55151297A>C | CA367576784 | EGFR | c.404A>C (p.Gln135Pro) n.753A>C c.563A>C (p.Gln188Pro) c.428A>C (p.Gln143Pro) c.89-4533A>C (n.89-4533A>C) | dbSNP |
| 7 | g.55151297A>G | CA367576785 | EGFR | c.404A>G (p.Gln135Arg) n.753A>G c.563A>G (p.Gln188Arg) c.428A>G (p.Gln143Arg) c.89-4533A>G (n.89-4533A>G) | ClinVar dbSNP gnomAD v4 |
| 7 | g.55151297A>T | CA367576786 | EGFR | c.404A>T (p.Gln135Leu) n.753A>T c.563A>T (p.Gln188Leu) c.428A>T (p.Gln143Leu) c.89-4533A>T (n.89-4533A>T) | |
| 7 | g.55151298A>C | CA367576787 | EGFR | c.405A>C (p.Gln135His) n.754A>C c.564A>C (p.Gln188His) c.429A>C (p.Gln143His) c.89-4532A>C (n.89-4532A>C) | |
| 7 | g.55151298A>G | CA454963257 | EGFR | c.405A>G (p.Gln135=) n.754A>G c.564A>G (p.Gln188=) c.429A>G (p.Gln143=) c.89-4532A>G (n.89-4532A>G) | gnomAD v4 |
| 7 | g.55151298A>T | CA367576788 | EGFR | c.405A>T (p.Gln135His) n.754A>T c.564A>T (p.Gln188His) c.429A>T (p.Gln143His) c.89-4532A>T (n.89-4532A>T) | dbSNP |
| 7 | g.55151299A>C | CA367576791 | EGFR | c.406A>C (p.Lys136Gln) n.755A>C c.565A>C (p.Lys189Gln) c.430A>C (p.Lys144Gln) c.89-4531A>C (n.89-4531A>C) | |
| 7 | g.55151299A>G | CA367576790 | EGFR | c.406A>G (p.Lys136Glu) n.755A>G c.565A>G (p.Lys189Glu) c.430A>G (p.Lys144Glu) c.89-4531A>G (n.89-4531A>G) | |
| 7 | g.55151299A>T | CA367576789 | EGFR | c.406A>T (p.Lys136Ter) n.755A>T c.565A>T (p.Lys189Ter) c.430A>T (p.Lys144Ter) c.89-4531A>T (n.89-4531A>T) | dbSNP |
| 7 | g.55151300A>C | CA367576792 | EGFR | c.407A>C (p.Lys136Thr) n.756A>C c.566A>C (p.Lys189Thr) c.431A>C (p.Lys144Thr) c.89-4530A>C (n.89-4530A>C) | COSMIC COSMIC |
| 7 | g.55151300A>G | CA367576793 | EGFR | c.407A>G (p.Lys136Arg) n.756A>G c.566A>G (p.Lys189Arg) c.431A>G (p.Lys144Arg) c.89-4530A>G (n.89-4530A>G) | |
| 7 | g.55151300A>T | CA367576794 | EGFR | c.407A>T (p.Lys136Met) n.756A>T c.566A>T (p.Lys189Met) c.431A>T (p.Lys144Met) c.89-4530A>T (n.89-4530A>T) | dbSNP |
| 7 | g.55151301G>A | CA4265266 | EGFR | c.408G>A (p.Lys136=) n.757G>A c.567G>A (p.Lys189=) c.432G>A (p.Lys144=) c.89-4529G>A (n.89-4529G>A) | dbSNP ExAC gnomAD v2 |
| 7 | g.55151301G>C | CA367576795 | EGFR | c.408G>C (p.Lys136Asn) n.757G>C c.567G>C (p.Lys189Asn) c.432G>C (p.Lys144Asn) c.89-4529G>C (n.89-4529G>C) | dbSNP |
| 7 | g.55151301G= | CA1708910310 | EGFR | c.408G= (p.Lys136=) n.757G= c.567G= (p.Lys189=) c.432G= (p.Lys144=) c.89-4529G= (n.89-4529G=) | |
| 7 | g.55151301G>T | CA367576796 | EGFR | c.408G>T (p.Lys136Asn) n.757G>T c.567G>T (p.Lys189Asn) c.432G>T (p.Lys144Asn) c.89-4529G>T (n.89-4529G>T) | ClinVar |
| 7 | g.55151302T>A | CA367576797 | EGFR | c.409T>A (p.Cys137Ser) n.758T>A c.568T>A (p.Cys190Ser) c.433T>A (p.Cys145Ser) c.89-4528T>A (n.89-4528T>A) | dbSNP |
| 7 | g.55151302T>C | CA367576799 | EGFR | c.409T>C (p.Cys137Arg) n.758T>C c.568T>C (p.Cys190Arg) c.433T>C (p.Cys145Arg) c.89-4528T>C (n.89-4528T>C) | |
| 7 | g.55151302T>G | CA367576798 | EGFR | c.409T>G (p.Cys137Gly) n.758T>G c.568T>G (p.Cys190Gly) c.433T>G (p.Cys145Gly) c.89-4528T>G (n.89-4528T>G) | |
| 7 | g.55151303G>A | CA367576800 | EGFR | c.410G>A (p.Cys137Tyr) n.759G>A c.569G>A (p.Cys190Tyr) c.434G>A (p.Cys145Tyr) c.89-4527G>A (n.89-4527G>A) | |
| 7 | g.55151303G>C | CA367576801 | EGFR | c.410G>C (p.Cys137Ser) n.759G>C c.569G>C (p.Cys190Ser) c.434G>C (p.Cys145Ser) c.89-4527G>C (n.89-4527G>C) | |
| 7 | g.55151303G>T | CA367576802 | EGFR | c.410G>T (p.Cys137Phe) n.759G>T c.569G>T (p.Cys190Phe) c.434G>T (p.Cys145Phe) c.89-4527G>T (n.89-4527G>T) | |
| 7 | g.55151304T>A | CA367576803 | EGFR | c.411T>A (p.Cys137Ter) n.760T>A c.570T>A (p.Cys190Ter) c.435T>A (p.Cys145Ter) c.89-4526T>A (n.89-4526T>A) | dbSNP |
| 7 | g.55151304T>C | CA454963286 | EGFR | c.411T>C (p.Cys137=) n.760T>C c.570T>C (p.Cys190=) c.435T>C (p.Cys145=) c.89-4526T>C (n.89-4526T>C) | dbSNP gnomAD v4 |
| 7 | g.55151304T>G | CA367576804 | EGFR | c.411T>G (p.Cys137Trp) n.760T>G c.570T>G (p.Cys190Trp) c.435T>G (p.Cys145Trp) c.89-4526T>G (n.89-4526T>G) | |
| 7 | g.55151305G>A | CA367576805 | EGFR | c.412G>A (p.Asp138Asn) n.761G>A c.571G>A (p.Asp191Asn) c.436G>A (p.Asp146Asn) c.89-4525G>A (n.89-4525G>A) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 7 | g.55151305G>C | CA367576806 | EGFR | c.412G>C (p.Asp138His) n.761G>C c.571G>C (p.Asp191His) c.436G>C (p.Asp146His) c.89-4525G>C (n.89-4525G>C) | dbSNP |
| 7 | g.55151305G= | CA1708910315 | EGFR | c.412G= (p.Asp138=) n.761G= c.571G= (p.Asp191=) c.436G= (p.Asp146=) c.89-4525G= (n.89-4525G=) | |
| 7 | g.55151305G>T | CA367576807 | EGFR | c.412G>T (p.Asp138Tyr) n.761G>T c.571G>T (p.Asp191Tyr) c.436G>T (p.Asp146Tyr) c.89-4525G>T (n.89-4525G>T) | |
| 7 | g.55151306A>C | CA367576808 | EGFR | c.413A>C (p.Asp138Ala) n.762A>C c.572A>C (p.Asp191Ala) c.437A>C (p.Asp146Ala) c.89-4524A>C (n.89-4524A>C) | |
| 7 | g.55151306A>G | CA367576809 | EGFR | c.413A>G (p.Asp138Gly) n.762A>G c.572A>G (p.Asp191Gly) c.437A>G (p.Asp146Gly) c.89-4524A>G (n.89-4524A>G) | |
| 7 | g.55151306A>T | CA367576810 | EGFR | c.413A>T (p.Asp138Val) n.762A>T c.572A>T (p.Asp191Val) c.437A>T (p.Asp146Val) c.89-4524A>T (n.89-4524A>T) | dbSNP |
| 7 | g.55151307T>A | CA367576812 | EGFR | c.414T>A (p.Asp138Glu) n.763T>A c.573T>A (p.Asp191Glu) c.438T>A (p.Asp146Glu) c.89-4523T>A (n.89-4523T>A) | ClinVar dbSNP gnomAD v4 |
| 7 | g.55151307T>C | CA454963302 | EGFR | c.414T>C (p.Asp138=) n.763T>C c.573T>C (p.Asp191=) c.438T>C (p.Asp146=) c.89-4523T>C (n.89-4523T>C) | |
| 7 | g.55151307T>G | CA367576811 | EGFR | c.414T>G (p.Asp138Glu) n.763T>G c.573T>G (p.Asp191Glu) c.438T>G (p.Asp146Glu) c.89-4523T>G (n.89-4523T>G) | |
| 7 | g.55151308C>A | CA4265267 | EGFR | c.415C>A (p.Pro139Thr) n.764C>A c.574C>A (p.Pro192Thr) c.439C>A (p.Pro147Thr) c.89-4522C>A (n.89-4522C>A) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 7 | g.55151308C= | CA1708910322 | EGFR | c.415C= (p.Pro139=) n.764C= c.574C= (p.Pro192=) c.439C= (p.Pro147=) c.89-4522C= (n.89-4522C=) | |
| 7 | g.55151308C>G | CA367576813 | EGFR | c.415C>G (p.Pro139Ala) n.764C>G c.574C>G (p.Pro192Ala) c.439C>G (p.Pro147Ala) c.89-4522C>G (n.89-4522C>G) | dbSNP |
| 7 | g.55151308C>T | CA367576814 | EGFR | c.415C>T (p.Pro139Ser) n.764C>T c.574C>T (p.Pro192Ser) c.439C>T (p.Pro147Ser) c.89-4522C>T (n.89-4522C>T) | |
| 7 | g.55151309C>A | CA367576815 | EGFR | c.416C>A (p.Pro139Gln) n.765C>A c.575C>A (p.Pro192Gln) c.440C>A (p.Pro147Gln) c.89-4521C>A (n.89-4521C>A) | |
| 7 | g.55151309C>G | CA367576816 | EGFR | c.416C>G (p.Pro139Arg) n.765C>G c.575C>G (p.Pro192Arg) c.440C>G (p.Pro147Arg) c.89-4521C>G (n.89-4521C>G) | |
| 7 | g.55151309C>T | CA367576817 | EGFR | c.416C>T (p.Pro139Leu) n.765C>T c.575C>T (p.Pro192Leu) c.440C>T (p.Pro147Leu) c.89-4521C>T (n.89-4521C>T) | ClinVar |
| 7 | g.55151310A>C | CA454963314 | EGFR | c.417A>C (p.Pro139=) n.766A>C c.576A>C (p.Pro192=) c.441A>C (p.Pro147=) c.89-4520A>C (n.89-4520A>C) | |
| 7 | g.55151310A>G | CA454963316 | EGFR | c.417A>G (p.Pro139=) n.766A>G c.576A>G (p.Pro192=) c.441A>G (p.Pro147=) c.89-4520A>G (n.89-4520A>G) | |
| 7 | g.55151310A>T | CA454963318 | EGFR | c.417A>T (p.Pro139=) n.766A>T c.576A>T (p.Pro192=) c.441A>T (p.Pro147=) c.89-4520A>T (n.89-4520A>T) | dbSNP |
| 7 | g.55151311A>C | CA367576820 | EGFR | c.418A>C (p.Ser140Arg) n.767A>C c.577A>C (p.Ser193Arg) c.442A>C (p.Ser148Arg) c.89-4519A>C (n.89-4519A>C) | |
| 7 | g.55151311A>G | CA367576819 | EGFR | c.418A>G (p.Ser140Gly) n.767A>G c.577A>G (p.Ser193Gly) c.442A>G (p.Ser148Gly) c.89-4519A>G (n.89-4519A>G) | ClinVar dbSNP |
| 7 | g.55151311A>T | CA367576818 | EGFR | c.418A>T (p.Ser140Cys) n.767A>T c.577A>T (p.Ser193Cys) c.442A>T (p.Ser148Cys) c.89-4519A>T (n.89-4519A>T) | dbSNP |
| 7 | g.55151312G>A | CA367576821 | EGFR | c.419G>A (p.Ser140Asn) n.768G>A c.578G>A (p.Ser193Asn) c.443G>A (p.Ser148Asn) c.89-4518G>A (n.89-4518G>A) | dbSNP gnomAD v4 |
| 7 | g.55151312G>C | CA367576822 | EGFR | c.419G>C (p.Ser140Thr) n.768G>C c.578G>C (p.Ser193Thr) c.443G>C (p.Ser148Thr) c.89-4518G>C (n.89-4518G>C) | dbSNP |
| 7 | g.55151312G= | CA1708910329 | EGFR | c.419G= (p.Ser140=) n.768G= c.578G= (p.Ser193=) c.443G= (p.Ser148=) c.89-4518G= (n.89-4518G=) | |
| 7 | g.55151312G>T | CA367576823 | EGFR | c.419G>T (p.Ser140Ile) n.768G>T c.578G>T (p.Ser193Ile) c.443G>T (p.Ser148Ile) c.89-4518G>T (n.89-4518G>T) | dbSNP |
| 7 | g.55151313C>A | CA367576824 | EGFR | c.420C>A (p.Ser140Arg) n.769C>A c.579C>A (p.Ser193Arg) c.444C>A (p.Ser148Arg) c.89-4517C>A (n.89-4517C>A) | dbSNP gnomAD v4 |
| 7 | g.55151313C= | CA1708910336 | EGFR | c.420C= (p.Ser140=) n.769C= c.579C= (p.Ser193=) c.444C= (p.Ser148=) c.89-4517C= (n.89-4517C=) | |
| 7 | g.55151313C>G | CA367576825 | EGFR | c.420C>G (p.Ser140Arg) n.769C>G c.579C>G (p.Ser193Arg) c.444C>G (p.Ser148Arg) c.89-4517C>G (n.89-4517C>G) | dbSNP |
| 7 | g.55151313C>T | CA4265268 | EGFR | c.420C>T (p.Ser140=) n.769C>T c.579C>T (p.Ser193=) c.444C>T (p.Ser148=) c.89-4517C>T (n.89-4517C>T) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 7 | g.55151314T>A | CA367576826 | EGFR | c.421T>A (p.Cys141Ser) n.770T>A c.580T>A (p.Cys194Ser) c.445T>A (p.Cys149Ser) c.89-4516T>A (n.89-4516T>A) | dbSNP |
| 7 | g.55151314T>C | CA367576828 | EGFR | c.421T>C (p.Cys141Arg) n.770T>C c.580T>C (p.Cys194Arg) c.445T>C (p.Cys149Arg) c.89-4516T>C (n.89-4516T>C) | |
| 7 | g.55151314T>G | CA367576827 | EGFR | c.421T>G (p.Cys141Gly) n.770T>G c.580T>G (p.Cys194Gly) c.445T>G (p.Cys149Gly) c.89-4516T>G (n.89-4516T>G) | |
| 7 | g.55151315G>A | CA367576829 | EGFR | c.422G>A (p.Cys141Tyr) n.771G>A c.581G>A (p.Cys194Tyr) c.446G>A (p.Cys149Tyr) c.89-4515G>A (n.89-4515G>A) | dbSNP |
| 7 | g.55151315G>C | CA367576830 | EGFR | c.422G>C (p.Cys141Ser) n.771G>C c.581G>C (p.Cys194Ser) c.446G>C (p.Cys149Ser) c.89-4515G>C (n.89-4515G>C) | ClinVar dbSNP gnomAD v4 |
| 7 | g.55151315G>T | CA367576831 | EGFR | c.422G>T (p.Cys141Phe) n.771G>T c.581G>T (p.Cys194Phe) c.446G>T (p.Cys149Phe) c.89-4515G>T (n.89-4515G>T) | |
| 7 | g.55151316T>A | CA367576832 | EGFR | c.423T>A (p.Cys141Ter) n.772T>A c.582T>A (p.Cys194Ter) c.447T>A (p.Cys149Ter) c.89-4514T>A (n.89-4514T>A) | gnomAD v4 |
| 7 | g.55151316T>C | CA4265269 | EGFR | c.423T>C (p.Cys141=) n.772T>C c.582T>C (p.Cys194=) c.447T>C (p.Cys149=) c.89-4514T>C (n.89-4514T>C) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 7 | g.55151316T>G | CA367576833 | EGFR | c.423T>G (p.Cys141Trp) n.772T>G c.582T>G (p.Cys194Trp) c.447T>G (p.Cys149Trp) c.89-4514T>G (n.89-4514T>G) | |
| 7 | g.55151316T= | CA1708910342 | EGFR | c.423T= (p.Cys141=) n.772T= c.582T= (p.Cys194=) c.447T= (p.Cys149=) c.89-4514T= (n.89-4514T=) | |
| 7 | g.55151317C>A | CA367576834 | EGFR | c.424C>A (p.Pro142Thr) n.773C>A c.583C>A (p.Pro195Thr) c.448C>A (p.Pro150Thr) c.89-4513C>A (n.89-4513C>A) | ClinVar dbSNP |
| 7 | g.55151317C>G | CA367576835 | EGFR | c.424C>G (p.Pro142Ala) n.773C>G c.583C>G (p.Pro195Ala) c.448C>G (p.Pro150Ala) c.89-4513C>G (n.89-4513C>G) | dbSNP |
| 7 | g.55151317C>T | CA367576836 | EGFR | c.424C>T (p.Pro142Ser) n.773C>T c.583C>T (p.Pro195Ser) c.448C>T (p.Pro150Ser) c.89-4513C>T (n.89-4513C>T) | dbSNP |
| 7 | g.55151318C>A | CA367576837 | EGFR | c.425C>A (p.Pro142His) n.774C>A c.584C>A (p.Pro195His) c.449C>A (p.Pro150His) c.89-4512C>A (n.89-4512C>A) | dbSNP gnomAD v4 |
| 7 | g.55151318C>G | CA367576838 | EGFR | c.425C>G (p.Pro142Arg) n.774C>G c.584C>G (p.Pro195Arg) c.449C>G (p.Pro150Arg) c.89-4512C>G (n.89-4512C>G) | dbSNP gnomAD v4 |
| 7 | g.55151318C>T | CA367576839 | EGFR | c.425C>T (p.Pro142Leu) n.774C>T c.584C>T (p.Pro195Leu) c.449C>T (p.Pro150Leu) c.89-4512C>T (n.89-4512C>T) | ClinVar dbSNP gnomAD v4 COSMIC COSMIC |
| 7 | g.55151319C>A | CA454963358 | EGFR | c.426C>A (p.Pro142=) n.775C>A c.585C>A (p.Pro195=) c.450C>A (p.Pro150=) c.89-4511C>A (n.89-4511C>A) | dbSNP |
| 7 | g.55151319C>G | CA454963363 | EGFR | c.426C>G (p.Pro142=) n.775C>G c.585C>G (p.Pro195=) c.450C>G (p.Pro150=) c.89-4511C>G (n.89-4511C>G) | |
| 7 | g.55151319C>T | CA454963360 | EGFR | c.426C>T (p.Pro142=) n.775C>T c.585C>T (p.Pro195=) c.450C>T (p.Pro150=) c.89-4511C>T (n.89-4511C>T) | dbSNP gnomAD v4 |
| 7 | g.55151320A= | CA1708910349 | EGFR | c.427A= (p.Asn143=) n.776A= c.586A= (p.Asn196=) c.451A= (p.Asn151=) c.89-4510A= (n.89-4510A=) | |
| 7 | g.55151320A>C | CA367576840 | EGFR | c.427A>C (p.Asn143His) n.776A>C c.586A>C (p.Asn196His) c.451A>C (p.Asn151His) c.89-4510A>C (n.89-4510A>C) | |
| 7 | g.55151320A>G | CA367576842 | EGFR | c.427A>G (p.Asn143Asp) n.776A>G c.586A>G (p.Asn196Asp) c.451A>G (p.Asn151Asp) c.89-4510A>G (n.89-4510A>G) | dbSNP gnomAD v3 gnomAD v4 |
| 7 | g.55151320A>T | CA367576841 | EGFR | c.427A>T (p.Asn143Tyr) n.776A>T c.586A>T (p.Asn196Tyr) c.451A>T (p.Asn151Tyr) c.89-4510A>T (n.89-4510A>T) | |
| 7 | g.55151321A= | CA1708910359 | EGFR | c.428A= (p.Asn143=) n.777A= c.587A= (p.Asn196=) c.452A= (p.Asn151=) c.89-4509A= (n.89-4509A=) | |
| 7 | g.55151321A>C | CA367576843 | EGFR | c.428A>C (p.Asn143Thr) n.777A>C c.587A>C (p.Asn196Thr) c.452A>C (p.Asn151Thr) c.89-4509A>C (n.89-4509A>C) | |
| 7 | g.55151321A>G | CA4265270 | EGFR | c.428A>G (p.Asn143Ser) n.777A>G c.587A>G (p.Asn196Ser) c.452A>G (p.Asn151Ser) c.89-4509A>G (n.89-4509A>G) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 7 | g.55151321A>T | CA367576844 | EGFR | c.428A>T (p.Asn143Ile) n.777A>T c.587A>T (p.Asn196Ile) c.452A>T (p.Asn151Ile) c.89-4509A>T (n.89-4509A>T) | |
| 7 | g.55151322T>A | CA367576845 | EGFR | c.429T>A (p.Asn143Lys) n.778T>A c.588T>A (p.Asn196Lys) c.453T>A (p.Asn151Lys) c.89-4508T>A (n.89-4508T>A) | |
| 7 | g.55151322T>C | CA454963380 | EGFR | c.429T>C (p.Asn143=) n.778T>C c.588T>C (p.Asn196=) c.453T>C (p.Asn151=) c.89-4508T>C (n.89-4508T>C) | |
| 7 | g.55151322T>G | CA367576846 | EGFR | c.429T>G (p.Asn143Lys) n.778T>G c.588T>G (p.Asn196Lys) c.453T>G (p.Asn151Lys) c.89-4508T>G (n.89-4508T>G) | |
| 7 | g.55151323G>A | CA367576847 | EGFR | c.430G>A (p.Gly144Arg) n.779G>A c.589G>A (p.Gly197Arg) c.454G>A (p.Gly152Arg) c.89-4507G>A (n.89-4507G>A) | dbSNP |
| 7 | g.55151323G>C | CA367576848 | EGFR | c.430G>C (p.Gly144Arg) n.779G>C c.589G>C (p.Gly197Arg) c.454G>C (p.Gly152Arg) c.89-4507G>C (n.89-4507G>C) | dbSNP |
| 7 | g.55151323G>T | CA367576849 | EGFR | c.430G>T (p.Gly144Trp) n.779G>T c.589G>T (p.Gly197Trp) c.454G>T (p.Gly152Trp) c.89-4507G>T (n.89-4507G>T) | |
| 7 | g.55151325del | CA2714933281 | EGFR | c.432del (p.Ser145AlafsTer13) n.781del c.591del (p.Ser198AlafsTer13) c.456del (p.Ser153AlafsTer13) c.89-4505del (n.89-4505del) | dbSNP |
| 7 | g.55151324G>A | CA367576850 | EGFR | c.431G>A (p.Gly144Glu) n.780G>A c.590G>A (p.Gly197Glu) c.455G>A (p.Gly152Glu) c.89-4506G>A (n.89-4506G>A) | dbSNP |
| 7 | g.55151324G>C | CA367576851 | EGFR | c.431G>C (p.Gly144Ala) n.780G>C c.590G>C (p.Gly197Ala) c.455G>C (p.Gly152Ala) c.89-4506G>C (n.89-4506G>C) | dbSNP |
| 7 | g.55151324G>T | CA367576852 | EGFR | c.431G>T (p.Gly144Val) n.780G>T c.590G>T (p.Gly197Val) c.455G>T (p.Gly152Val) c.89-4506G>T (n.89-4506G>T) | dbSNP |
| 7 | g.55151325G>A | CA454963390 | EGFR | c.432G>A (p.Gly144=) n.781G>A c.591G>A (p.Gly197=) c.456G>A (p.Gly152=) c.89-4505G>A (n.89-4505G>A) | ClinVar dbSNP gnomAD v4 COSMIC COSMIC |
| 7 | g.55151325G>C | CA454963392 | EGFR | c.432G>C (p.Gly144=) n.781G>C c.591G>C (p.Gly197=) c.456G>C (p.Gly152=) c.89-4505G>C (n.89-4505G>C) | dbSNP |
| 7 | g.55151325G>T | CA454963395 | EGFR | c.432G>T (p.Gly144=) n.781G>T c.591G>T (p.Gly197=) c.456G>T (p.Gly152=) c.89-4505G>T (n.89-4505G>T) | dbSNP |
| 7 | g.55151326A>C | CA367576853 | EGFR | c.433A>C (p.Ser145Arg) n.782A>C c.592A>C (p.Ser198Arg) c.457A>C (p.Ser153Arg) c.89-4504A>C (n.89-4504A>C) | |
| 7 | g.55151326A>G | CA367576854 | EGFR | c.433A>G (p.Ser145Gly) n.782A>G c.592A>G (p.Ser198Gly) c.457A>G (p.Ser153Gly) c.89-4504A>G (n.89-4504A>G) | ClinVar dbSNP gnomAD v4 |
| 7 | g.55151326A>T | CA367576855 | EGFR | c.433A>T (p.Ser145Cys) n.782A>T c.592A>T (p.Ser198Cys) c.457A>T (p.Ser153Cys) c.89-4504A>T (n.89-4504A>T) | dbSNP |
| 7 | g.55151327G>A | CA367576858 | EGFR | c.434G>A (p.Ser145Asn) n.783G>A c.593G>A (p.Ser198Asn) c.458G>A (p.Ser153Asn) c.89-4503G>A (n.89-4503G>A) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 7 | g.55151327G>C | CA367576856 | EGFR | c.434G>C (p.Ser145Thr) n.783G>C c.593G>C (p.Ser198Thr) c.458G>C (p.Ser153Thr) c.89-4503G>C (n.89-4503G>C) | dbSNP |
| 7 | g.55151327G= | CA1708910375 | EGFR | c.434G= (p.Ser145=) n.783G= c.593G= (p.Ser198=) c.458G= (p.Ser153=) c.89-4503G= (n.89-4503G=) | |
| 7 | g.55151327G>T | CA367576857 | EGFR | c.434G>T (p.Ser145Ile) n.783G>T c.593G>T (p.Ser198Ile) c.458G>T (p.Ser153Ile) c.89-4503G>T (n.89-4503G>T) | |
| 7 | g.55151328C>A | CA367576859 | EGFR | c.435C>A (p.Ser145Arg) n.784C>A c.594C>A (p.Ser198Arg) c.459C>A (p.Ser153Arg) c.89-4502C>A (n.89-4502C>A) | dbSNP COSMIC COSMIC |
| 7 | g.55151328C= | CA1708910384 | EGFR | c.435C= (p.Ser145=) n.784C= c.594C= (p.Ser198=) c.459C= (p.Ser153=) c.89-4502C= (n.89-4502C=) | |
| 7 | g.55151328C>G | CA367576860 | EGFR | c.435C>G (p.Ser145Arg) n.784C>G c.594C>G (p.Ser198Arg) c.459C>G (p.Ser153Arg) c.89-4502C>G (n.89-4502C>G) | dbSNP |
| 7 | g.55151328C>T | CA4265271 | EGFR | c.435C>T (p.Ser145=) n.784C>T c.594C>T (p.Ser198=) c.459C>T (p.Ser153=) c.89-4502C>T (n.89-4502C>T) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC |
| 7 | g.55151329T>A | CA367576861 | EGFR | c.436T>A (p.Cys146Ser) n.785T>A c.595T>A (p.Cys199Ser) c.460T>A (p.Cys154Ser) c.89-4501T>A (n.89-4501T>A) | dbSNP |
| 7 | g.55151329T>C | CA367576862 | EGFR | c.436T>C (p.Cys146Arg) n.785T>C c.595T>C (p.Cys199Arg) c.460T>C (p.Cys154Arg) c.89-4501T>C (n.89-4501T>C) | |
| 7 | g.55151329T>G | CA367576863 | EGFR | c.436T>G (p.Cys146Gly) n.785T>G c.595T>G (p.Cys199Gly) c.460T>G (p.Cys154Gly) c.89-4501T>G (n.89-4501T>G) | |
| 7 | g.55151330G>A | CA367576864 | EGFR | c.437G>A (p.Cys146Tyr) n.786G>A c.596G>A (p.Cys199Tyr) c.461G>A (p.Cys154Tyr) c.89-4500G>A (n.89-4500G>A) | dbSNP |
| 7 | g.55151330G>C | CA367576865 | EGFR | c.437G>C (p.Cys146Ser) n.786G>C c.596G>C (p.Cys199Ser) c.461G>C (p.Cys154Ser) c.89-4500G>C (n.89-4500G>C) | dbSNP COSMIC COSMIC COSMIC COSMIC |
| 7 | g.55151330G>T | CA367576866 | EGFR | c.437G>T (p.Cys146Phe) n.786G>T c.596G>T (p.Cys199Phe) c.461G>T (p.Cys154Phe) c.89-4500G>T (n.89-4500G>T) | gnomAD v4 |
| 7 | g.55151331C>A | CA367576867 | EGFR | c.438C>A (p.Cys146Ter) n.787C>A c.597C>A (p.Cys199Ter) c.462C>A (p.Cys154Ter) c.89-4499C>A (n.89-4499C>A) | |
| 7 | g.55151331C>G | CA367576868 | EGFR | c.438C>G (p.Cys146Trp) n.787C>G c.597C>G (p.Cys199Trp) c.462C>G (p.Cys154Trp) c.89-4499C>G (n.89-4499C>G) | dbSNP |
| 7 | g.55151331C>T | CA454963425 | EGFR | c.438C>T (p.Cys146=) n.787C>T c.597C>T (p.Cys199=) c.462C>T (p.Cys154=) c.89-4499C>T (n.89-4499C>T) | ClinVar dbSNP |
| 7 | g.55151332T>A | CA367576870 | EGFR | c.439T>A (p.Trp147Arg) n.788T>A c.598T>A (p.Trp200Arg) c.463T>A (p.Trp155Arg) c.89-4498T>A (n.89-4498T>A) | gnomAD v4 |
| 7 | g.55151332T>C | CA367576871 | EGFR | c.439T>C (p.Trp147Arg) n.788T>C c.598T>C (p.Trp200Arg) c.463T>C (p.Trp155Arg) c.89-4498T>C (n.89-4498T>C) | |
| 7 | g.55151332T>G | CA367576869 | EGFR | c.439T>G (p.Trp147Gly) n.788T>G c.598T>G (p.Trp200Gly) c.463T>G (p.Trp155Gly) c.89-4498T>G (n.89-4498T>G) | gnomAD v4 |
| 7 | g.55151333G>A | CA367576872 | EGFR | c.440G>A (p.Trp147Ter) n.789G>A c.599G>A (p.Trp200Ter) c.464G>A (p.Trp155Ter) c.89-4497G>A (n.89-4497G>A) | dbSNP COSMIC COSMIC |
| 7 | g.55151333G>C | CA367576873 | EGFR | c.440G>C (p.Trp147Ser) n.789G>C c.599G>C (p.Trp200Ser) c.464G>C (p.Trp155Ser) c.89-4497G>C (n.89-4497G>C) | |
| 7 | g.55151333G>T | CA367576874 | EGFR | c.440G>T (p.Trp147Leu) n.789G>T c.599G>T (p.Trp200Leu) c.464G>T (p.Trp155Leu) c.89-4497G>T (n.89-4497G>T) | dbSNP |
| 7 | g.55151334G>A | CA367576875 | EGFR | c.441G>A (p.Trp147Ter) n.790G>A c.600G>A (p.Trp200Ter) c.465G>A (p.Trp155Ter) c.89-4496G>A (n.89-4496G>A) | dbSNP |
| 7 | g.55151334G>C | CA367576876 | EGFR | c.441G>C (p.Trp147Cys) n.790G>C c.600G>C (p.Trp200Cys) c.465G>C (p.Trp155Cys) c.89-4496G>C (n.89-4496G>C) | dbSNP |
| 7 | g.55151334G>T | CA367576877 | EGFR | c.441G>T (p.Trp147Cys) n.790G>T c.600G>T (p.Trp200Cys) c.465G>T (p.Trp155Cys) c.89-4496G>T (n.89-4496G>T) | dbSNP gnomAD v4 |
| 7 | g.55151335G>A | CA367576878 | EGFR | c.442G>A (p.Gly148Ser) n.791G>A c.601G>A (p.Gly201Ser) c.466G>A (p.Gly156Ser) c.89-4495G>A (n.89-4495G>A) | dbSNP |
| 7 | g.55151335G>C | CA367576879 | EGFR | c.442G>C (p.Gly148Arg) n.791G>C c.601G>C (p.Gly201Arg) c.466G>C (p.Gly156Arg) c.89-4495G>C (n.89-4495G>C) | dbSNP |
| 7 | g.55151335G>T | CA367576880 | EGFR | c.442G>T (p.Gly148Cys) n.791G>T c.601G>T (p.Gly201Cys) c.466G>T (p.Gly156Cys) c.89-4495G>T (n.89-4495G>T) | |
| 7 | g.55151336G>A | CA367576881 | EGFR | c.443G>A (p.Gly148Asp) n.792G>A c.602G>A (p.Gly201Asp) c.467G>A (p.Gly156Asp) c.89-4494G>A (n.89-4494G>A) | dbSNP |
| 7 | g.55151336G>C | CA367576882 | EGFR | c.443G>C (p.Gly148Ala) n.792G>C c.602G>C (p.Gly201Ala) c.467G>C (p.Gly156Ala) c.89-4494G>C (n.89-4494G>C) | dbSNP |
| 7 | g.55151336G>T | CA367576884 | EGFR | c.443G>T (p.Gly148Val) n.792G>T c.602G>T (p.Gly201Val) c.467G>T (p.Gly156Val) c.89-4494G>T (n.89-4494G>T) | dbSNP |
| 7 | g.55151337T>A | CA454963455 | EGFR | c.444T>A (p.Gly148=) n.793T>A c.603T>A (p.Gly201=) c.468T>A (p.Gly156=) c.89-4493T>A (n.89-4493T>A) | dbSNP |
| 7 | g.55151337T>C | CA454963451 | EGFR | c.444T>C (p.Gly148=) n.793T>C c.603T>C (p.Gly201=) c.468T>C (p.Gly156=) c.89-4493T>C (n.89-4493T>C) | |
| 7 | g.55151337T>G | CA454963453 | EGFR | c.444T>G (p.Gly148=) n.793T>G c.603T>G (p.Gly201=) c.468T>G (p.Gly156=) c.89-4493T>G (n.89-4493T>G) | dbSNP |
| 7 | g.55151338G>A | CA367576886 | EGFR | c.445G>A (p.Ala149Thr) n.794G>A c.604G>A (p.Ala202Thr) c.469G>A (p.Ala157Thr) c.89-4492G>A (n.89-4492G>A) | dbSNP |
| 7 | g.55151338G>C | CA367576887 | EGFR | c.445G>C (p.Ala149Pro) n.794G>C c.604G>C (p.Ala202Pro) c.469G>C (p.Ala157Pro) c.89-4492G>C (n.89-4492G>C) | |
| 7 | g.55151338G>T | CA367576885 | EGFR | c.445G>T (p.Ala149Ser) n.794G>T c.604G>T (p.Ala202Ser) c.469G>T (p.Ala157Ser) c.89-4492G>T (n.89-4492G>T) | |
| 7 | g.55151339C>A | CA367576888 | EGFR | c.446C>A (p.Ala149Glu) n.795C>A c.605C>A (p.Ala202Glu) c.470C>A (p.Ala157Glu) c.89-4491C>A (n.89-4491C>A) | |
| 7 | g.55151339C>G | CA367576889 | EGFR | c.446C>G (p.Ala149Gly) n.795C>G c.605C>G (p.Ala202Gly) c.470C>G (p.Ala157Gly) c.89-4491C>G (n.89-4491C>G) | dbSNP |
| 7 | g.55151339C>T | CA367576890 | EGFR | c.446C>T (p.Ala149Val) n.795C>T c.605C>T (p.Ala202Val) c.470C>T (p.Ala157Val) c.89-4491C>T (n.89-4491C>T) | dbSNP |
| 7 | g.55151340A= | CA1708910400 | EGFR | c.447A= (p.Ala149=) n.796A= c.606A= (p.Ala202=) c.471A= (p.Ala157=) c.89-4490A= (n.89-4490A=) | |
| 7 | g.55151340A>C | CA4265272 | EGFR | c.447A>C (p.Ala149=) n.796A>C c.606A>C (p.Ala202=) c.471A>C (p.Ala157=) c.89-4490A>C (n.89-4490A>C) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 7 | g.55151340A>G | CA454963469 | EGFR | c.447A>G (p.Ala149=) n.796A>G c.606A>G (p.Ala202=) c.471A>G (p.Ala157=) c.89-4490A>G (n.89-4490A>G) | dbSNP COSMIC COSMIC COSMIC COSMIC |
| 7 | g.55151340A>T | CA454963472 | EGFR | c.447A>T (p.Ala149=) n.796A>T c.606A>T (p.Ala202=) c.471A>T (p.Ala157=) c.89-4490A>T (n.89-4490A>T) | dbSNP |
| 7 | g.55151341G>A | CA367576893 | EGFR | c.448G>A (p.Gly150Arg) n.797G>A c.607G>A (p.Gly203Arg) c.472G>A (p.Gly158Arg) c.89-4489G>A (n.89-4489G>A) | ClinVar dbSNP COSMIC COSMIC |
| 7 | g.55151341G>C | CA367576892 | EGFR | c.448G>C (p.Gly150Arg) n.797G>C c.607G>C (p.Gly203Arg) c.472G>C (p.Gly158Arg) c.89-4489G>C (n.89-4489G>C) | |
| 7 | g.55151341G= | CA1708910406 | EGFR | c.448G= (p.Gly150=) n.797G= c.607G= (p.Gly203=) c.472G= (p.Gly158=) c.89-4489G= (n.89-4489G=) | |
| 7 | g.55151341G>T | CA367576891 | EGFR | c.448G>T (p.Gly150Ter) n.797G>T c.607G>T (p.Gly203Ter) c.472G>T (p.Gly158Ter) c.89-4489G>T (n.89-4489G>T) | |
| 7 | g.55151342G>A | CA367576894 | EGFR | c.449G>A (p.Gly150Glu) n.798G>A c.608G>A (p.Gly203Glu) c.473G>A (p.Gly158Glu) c.89-4488G>A (n.89-4488G>A) | dbSNP COSMIC COSMIC |
| 7 | g.55151342G>C | CA367576895 | EGFR | c.449G>C (p.Gly150Ala) n.798G>C c.608G>C (p.Gly203Ala) c.473G>C (p.Gly158Ala) c.89-4488G>C (n.89-4488G>C) | dbSNP |
| 7 | g.55151342G>T | CA367576896 | EGFR | c.449G>T (p.Gly150Val) n.798G>T c.608G>T (p.Gly203Val) c.473G>T (p.Gly158Val) c.89-4488G>T (n.89-4488G>T) | |
| 7 | g.55151343A>C | CA454963488 | EGFR | c.450A>C (p.Gly150=) n.799A>C c.609A>C (p.Gly203=) c.474A>C (p.Gly158=) c.89-4487A>C (n.89-4487A>C) | ClinVar |
| 7 | g.55151343A>G | CA454963483 | EGFR | c.450A>G (p.Gly150=) n.799A>G c.609A>G (p.Gly203=) c.474A>G (p.Gly158=) c.89-4487A>G (n.89-4487A>G) | |
| 7 | g.55151343A>T | CA454963485 | EGFR | c.450A>T (p.Gly150=) n.799A>T c.609A>T (p.Gly203=) c.474A>T (p.Gly158=) c.89-4487A>T (n.89-4487A>T) | gnomAD v4 |
| 7 | g.55151343_55151346delinsAGAG | CA1708910408 | EGFR | c.450_453delinsAGAG (p.Gly150=) n.799_802delinsAGAG c.609_612delinsAGAG (p.Gly203=) c.474_477delinsAGAG (p.Gly158=) c.89-4487_89-4484delinsAGAG (n.89-4487_89-4484delinsAGAG) | |
| 7 | g.55151344G>A | CA4265273 | EGFR | c.451G>A (p.Glu151Lys) n.800G>A c.610G>A (p.Glu204Lys) c.475G>A (p.Glu159Lys) c.89-4486G>A (n.89-4486G>A) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC |
| 7 | g.55151344G>C | CA367576899 | EGFR | c.451G>C (p.Glu151Gln) n.800G>C c.610G>C (p.Glu204Gln) c.475G>C (p.Glu159Gln) c.89-4486G>C (n.89-4486G>C) | dbSNP |
| 7 | g.55151344G= | CA1708910416 | EGFR | c.451G= (p.Glu151=) n.800G= c.610G= (p.Glu204=) c.475G= (p.Glu159=) c.89-4486G= (n.89-4486G=) | |
| 7 | g.55151344G>T | CA367576901 | EGFR | c.451G>T (p.Glu151Ter) n.800G>T c.610G>T (p.Glu204Ter) c.475G>T (p.Glu159Ter) c.89-4486G>T (n.89-4486G>T) | |
| 7 | g.55151347_55151349del | CA1708910410 | EGFR | c.454_456del (p.Glu152del) n.803_805del c.613_615del (p.Glu205del) c.478_480del (p.Glu160del) c.89-4483_89-4481del (n.89-4483_89-4481del) | ClinVar dbSNP |
| 7 | g.55151345A>C | CA367577255 | EGFR | c.452A>C (p.Glu151Ala) n.801A>C c.611A>C (p.Glu204Ala) c.476A>C (p.Glu159Ala) c.89-4485A>C (n.89-4485A>C) | |
| 7 | g.55151345A>G | CA367577257 | EGFR | c.452A>G (p.Glu151Gly) n.801A>G c.611A>G (p.Glu204Gly) c.476A>G (p.Glu159Gly) c.89-4485A>G (n.89-4485A>G) | dbSNP |
| 7 | g.55151345A>T | CA367577256 | EGFR | c.452A>T (p.Glu151Val) n.801A>T c.611A>T (p.Glu204Val) c.476A>T (p.Glu159Val) c.89-4485A>T (n.89-4485A>T) | |
| 7 | g.55151346G>A | CA454963888 | EGFR | c.453G>A (p.Glu151=) n.802G>A c.612G>A (p.Glu204=) c.477G>A (p.Glu159=) c.89-4484G>A (n.89-4484G>A) | ClinVar dbSNP |
| 7 | g.55151346G>C | CA367577258 | EGFR | c.453G>C (p.Glu151Asp) n.802G>C c.612G>C (p.Glu204Asp) c.477G>C (p.Glu159Asp) c.89-4484G>C (n.89-4484G>C) | |
| 7 | g.55151346G>T | CA367577259 | EGFR | c.453G>T (p.Glu151Asp) n.802G>T c.612G>T (p.Glu204Asp) c.477G>T (p.Glu159Asp) c.89-4484G>T (n.89-4484G>T) | dbSNP |
| 7 | g.55151347G>A | CA367577260 | EGFR | c.454G>A (p.Glu152Lys) n.803G>A c.613G>A (p.Glu205Lys) c.478G>A (p.Glu160Lys) c.89-4483G>A (n.89-4483G>A) | ClinVar dbSNP |
| 7 | g.55151347G>C | CA367577262 | EGFR | c.454G>C (p.Glu152Gln) n.803G>C c.613G>C (p.Glu205Gln) c.478G>C (p.Glu160Gln) c.89-4483G>C (n.89-4483G>C) | dbSNP |
| 7 | g.55151347G>T | CA367577261 | EGFR | c.454G>T (p.Glu152Ter) n.803G>T c.613G>T (p.Glu205Ter) c.478G>T (p.Glu160Ter) c.89-4483G>T (n.89-4483G>T) | |
| 7 | g.55151348A>C | CA367577263 | EGFR | c.455A>C (p.Glu152Ala) n.804A>C c.614A>C (p.Glu205Ala) c.479A>C (p.Glu160Ala) c.89-4482A>C (n.89-4482A>C) | |
| 7 | g.55151348A>G | CA367577264 | EGFR | c.455A>G (p.Glu152Gly) n.804A>G c.614A>G (p.Glu205Gly) c.479A>G (p.Glu160Gly) c.89-4482A>G (n.89-4482A>G) | dbSNP |
| 7 | g.55151348A>T | CA367577265 | EGFR | c.455A>T (p.Glu152Val) n.804A>T c.614A>T (p.Glu205Val) c.479A>T (p.Glu160Val) c.89-4482A>T (n.89-4482A>T) | dbSNP |
| 7 | g.55151349G>A | CA454963907 | EGFR | c.456G>A (p.Glu152=) n.805G>A c.615G>A (p.Glu205=) c.480G>A (p.Glu160=) c.89-4481G>A (n.89-4481G>A) | dbSNP |
| 7 | g.55151349G>C | CA367577266 | EGFR | c.456G>C (p.Glu152Asp) n.805G>C c.615G>C (p.Glu205Asp) c.480G>C (p.Glu160Asp) c.89-4481G>C (n.89-4481G>C) | ClinVar dbSNP |
| 7 | g.55151349G= | CA1708910420 | EGFR | c.456G= (p.Glu152=) n.805G= c.615G= (p.Glu205=) c.480G= (p.Glu160=) c.89-4481G= (n.89-4481G=) | |
| 7 | g.55151349G>T | CA367577267 | EGFR | c.456G>T (p.Glu152Asp) n.805G>T c.615G>T (p.Glu205Asp) c.480G>T (p.Glu160Asp) c.89-4481G>T (n.89-4481G>T) | gnomAD v4 |
| 7 | g.55151350A>C | CA367577268 | EGFR | c.457A>C (p.Asn153His) n.806A>C c.616A>C (p.Asn206His) c.481A>C (p.Asn161His) c.89-4480A>C (n.89-4480A>C) | |
| 7 | g.55151350A>G | CA367577269 | EGFR | c.457A>G (p.Asn153Asp) n.806A>G c.616A>G (p.Asn206Asp) c.481A>G (p.Asn161Asp) c.89-4480A>G (n.89-4480A>G) | |
| 7 | g.55151350A>T | CA367577270 | EGFR | c.457A>T (p.Asn153Tyr) n.806A>T c.616A>T (p.Asn206Tyr) c.481A>T (p.Asn161Tyr) c.89-4480A>T (n.89-4480A>T) | |
| 7 | g.55151351A>C | CA367577271 | EGFR | c.458A>C (p.Asn153Thr) n.807A>C c.617A>C (p.Asn206Thr) c.482A>C (p.Asn161Thr) c.89-4479A>C (n.89-4479A>C) | |
| 7 | g.55151351A>G | CA367577272 | EGFR | c.458A>G (p.Asn153Ser) n.807A>G c.617A>G (p.Asn206Ser) c.482A>G (p.Asn161Ser) c.89-4479A>G (n.89-4479A>G) | |
| 7 | g.55151351A>T | CA367577273 | EGFR | c.458A>T (p.Asn153Ile) n.807A>T c.617A>T (p.Asn206Ile) c.482A>T (p.Asn161Ile) c.89-4479A>T (n.89-4479A>T) | dbSNP |
| 7 | g.55151352C>A | CA367577275 | EGFR | c.459C>A (p.Asn153Lys) n.808C>A c.618C>A (p.Asn206Lys) c.483C>A (p.Asn161Lys) c.89-4478C>A (n.89-4478C>A) | dbSNP |
| 7 | g.55151352C>G | CA367577274 | EGFR | c.459C>G (p.Asn153Lys) n.808C>G c.618C>G (p.Asn206Lys) c.483C>G (p.Asn161Lys) c.89-4478C>G (n.89-4478C>G) | dbSNP |
| 7 | g.55151352C>T | CA454963926 | EGFR | c.459C>T (p.Asn153=) n.808C>T c.618C>T (p.Asn206=) c.483C>T (p.Asn161=) c.89-4478C>T (n.89-4478C>T) | dbSNP |
| 7 | g.55151353T>A | CA367577276 | EGFR | c.460T>A (p.Cys154Ser) n.809T>A c.619T>A (p.Cys207Ser) c.484T>A (p.Cys162Ser) c.89-4477T>A (n.89-4477T>A) | dbSNP |
| 7 | g.55151353T>C | CA367577277 | EGFR | c.460T>C (p.Cys154Arg) n.809T>C c.619T>C (p.Cys207Arg) c.484T>C (p.Cys162Arg) c.89-4477T>C (n.89-4477T>C) | gnomAD v4 |
| 7 | g.55151353T>G | CA367577278 | EGFR | c.460T>G (p.Cys154Gly) n.809T>G c.619T>G (p.Cys207Gly) c.484T>G (p.Cys162Gly) c.89-4477T>G (n.89-4477T>G) | |
| 7 | g.55151354G>A | CA367577279 | EGFR | c.461G>A (p.Cys154Tyr) n.810G>A c.620G>A (p.Cys207Tyr) c.485G>A (p.Cys162Tyr) c.89-4476G>A (n.89-4476G>A) | |
| 7 | g.55151354G>C | CA367577280 | EGFR | c.461G>C (p.Cys154Ser) n.810G>C c.620G>C (p.Cys207Ser) c.485G>C (p.Cys162Ser) c.89-4476G>C (n.89-4476G>C) | |
| 7 | g.55151354G>T | CA367577281 | EGFR | c.461G>T (p.Cys154Phe) n.810G>T c.620G>T (p.Cys207Phe) c.485G>T (p.Cys162Phe) c.89-4476G>T (n.89-4476G>T) | gnomAD v4 |
| 7 | g.55151355C>A | CA367577282 | EGFR | c.462C>A (p.Cys154Ter) n.811C>A c.621C>A (p.Cys207Ter) c.486C>A (p.Cys162Ter) c.89-4475C>A (n.89-4475C>A) | dbSNP |
| 7 | g.55151355C>G | CA367577283 | EGFR | c.462C>G (p.Cys154Trp) n.811C>G c.621C>G (p.Cys207Trp) c.486C>G (p.Cys162Trp) c.89-4475C>G (n.89-4475C>G) | dbSNP |
| 7 | g.55151355C>T | CA454963942 | EGFR | c.462C>T (p.Cys154=) n.811C>T c.621C>T (p.Cys207=) c.486C>T (p.Cys162=) c.89-4475C>T (n.89-4475C>T) | dbSNP |
| 7 | g.55151356C>A | CA367577284 | EGFR | c.463C>A (p.Gln155Lys) n.812C>A c.622C>A (p.Gln208Lys) c.487C>A (p.Gln163Lys) c.89-4474C>A (n.89-4474C>A) | |
| 7 | g.55151356C>G | CA367577285 | EGFR | c.463C>G (p.Gln155Glu) n.812C>G c.622C>G (p.Gln208Glu) c.487C>G (p.Gln163Glu) c.89-4474C>G (n.89-4474C>G) | dbSNP |
| 7 | g.55151356C>T | CA367577286 | EGFR | c.463C>T (p.Gln155Ter) n.812C>T c.622C>T (p.Gln208Ter) c.487C>T (p.Gln163Ter) c.89-4474C>T (n.89-4474C>T) | dbSNP COSMIC COSMIC COSMIC COSMIC |
| 7 | g.55151357A>C | CA367577288 | EGFR | c.464A>C (p.Gln155Pro) n.813A>C c.623A>C (p.Gln208Pro) c.488A>C (p.Gln163Pro) c.89-4473A>C (n.89-4473A>C) | |
| 7 | g.55151357A>G | CA367577289 | EGFR | c.464A>G (p.Gln155Arg) n.813A>G c.623A>G (p.Gln208Arg) c.488A>G (p.Gln163Arg) c.89-4473A>G (n.89-4473A>G) | |
| 7 | g.55151357A>T | CA367577287 | EGFR | c.464A>T (p.Gln155Leu) n.813A>T c.623A>T (p.Gln208Leu) c.488A>T (p.Gln163Leu) c.89-4473A>T (n.89-4473A>T) | |
| 7 | g.55151358G>A | CA4265274 | EGFR | c.465G>A (p.Gln155=) n.814G>A c.624G>A (p.Gln208=) c.489G>A (p.Gln163=) c.89-4472G>A (n.89-4472G>A) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 7 | g.55151358G>C | CA367577290 | EGFR | c.465G>C (p.Gln155His) n.814G>C c.624G>C (p.Gln208His) c.489G>C (p.Gln163His) c.89-4472G>C (n.89-4472G>C) | |
| 7 | g.55151358G= | CA1708910424 | EGFR | c.465G= (p.Gln155=) n.814G= c.624G= (p.Gln208=) c.489G= (p.Gln163=) c.89-4472G= (n.89-4472G=) | |
| 7 | g.55151358G>T | CA367577291 | EGFR | c.465G>T (p.Gln155His) n.814G>T c.624G>T (p.Gln208His) c.489G>T (p.Gln163His) c.89-4472G>T (n.89-4472G>T) | |
| 7 | g.55151359A>C | CA367577292 | EGFR | c.466A>C (p.Lys156Gln) n.815A>C c.625A>C (p.Lys209Gln) c.490A>C (p.Lys164Gln) c.89-4471A>C (n.89-4471A>C) | |
| 7 | g.55151359A>G | CA367577293 | EGFR | c.466A>G (p.Lys156Glu) n.815A>G c.625A>G (p.Lys209Glu) c.490A>G (p.Lys164Glu) c.89-4471A>G (n.89-4471A>G) | |
| 7 | g.55151359A>T | CA367577294 | EGFR | c.466A>T (p.Lys156Ter) n.815A>T c.625A>T (p.Lys209Ter) c.490A>T (p.Lys164Ter) c.89-4471A>T (n.89-4471A>T) | |
| 7 | g.55151360A>C | CA367577295 | EGFR | c.467A>C (p.Lys156Thr) n.816A>C c.626A>C (p.Lys209Thr) c.491A>C (p.Lys164Thr) c.89-4470A>C (n.89-4470A>C) | |
| 7 | g.55151360A>G | CA367577296 | EGFR | c.467A>G (p.Lys156Arg) n.816A>G c.626A>G (p.Lys209Arg) c.491A>G (p.Lys164Arg) c.89-4470A>G (n.89-4470A>G) | |
| 7 | g.55151360A>T | CA367577297 | EGFR | c.467A>T (p.Lys156Ile) n.816A>T c.626A>T (p.Lys209Ile) c.491A>T (p.Lys164Ile) c.89-4470A>T (n.89-4470A>T) | |
| 7 | g.55151361A>C | CA367577298 | EGFR | c.468A>C (p.Lys156Asn) n.817A>C c.627A>C (p.Lys209Asn) c.492A>C (p.Lys164Asn) c.89-4469A>C (n.89-4469A>C) | COSMIC COSMIC |
| 7 | g.55151361A>G | CA454963969 | EGFR | c.468A>G (p.Lys156=) n.817A>G c.627A>G (p.Lys209=) c.492A>G (p.Lys164=) c.89-4469A>G (n.89-4469A>G) | gnomAD v4 |
| 7 | g.55151361A>T | CA367577299 | EGFR | c.468A>T (p.Lys156Asn) n.817A>T c.627A>T (p.Lys209Asn) c.492A>T (p.Lys164Asn) c.89-4469A>T (n.89-4469A>T) | dbSNP |
| 7 | g.55151362C>A | CA367577300 | EGFR | c.469C>A (p.Leu157Met) n.818C>A c.628C>A (p.Leu210Met) c.493C>A (p.Leu165Met) c.89-4468C>A (n.89-4468C>A) | dbSNP |
| 7 | g.55151362C= | CA1708910433 | EGFR | c.469C= (p.Leu157=) n.818C= c.628C= (p.Leu210=) c.493C= (p.Leu165=) c.89-4468C= (n.89-4468C=) | |
| 7 | g.55151362C>G | CA367577301 | EGFR | c.469C>G (p.Leu157Val) n.818C>G c.628C>G (p.Leu210Val) c.493C>G (p.Leu165Val) c.89-4468C>G (n.89-4468C>G) | dbSNP |
| 7 | g.55151362C>T | CA454963977 | EGFR | c.469C>T (p.Leu157=) n.818C>T c.628C>T (p.Leu210=) c.493C>T (p.Leu165=) c.89-4468C>T (n.89-4468C>T) | ClinVar dbSNP gnomAD v4 COSMIC COSMIC COSMIC COSMIC |
| 7 | g.55151363G>A | CA367577304 | EGFR | c.469+1G>A (n.469+1G>A) n.818+1G>A c.628+1G>A (n.628+1G>A) c.493+1G>A (n.493+1G>A) c.89-4467G>A (n.89-4467G>A) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 7 | g.55151363G>C | CA367577303 | EGFR | c.469+1G>C (n.469+1G>C) n.818+1G>C c.628+1G>C (n.628+1G>C) c.493+1G>C (n.493+1G>C) c.89-4467G>C (n.89-4467G>C) | dbSNP gnomAD v4 |
| 7 | g.55151363G= | CA1708910439 | EGFR | c.469+1G= (n.469+1G=) n.818+1G= c.628+1G= (n.628+1G=) c.493+1G= (n.493+1G=) c.89-4467G= (n.89-4467G=) | |
| 7 | g.55151363G>T | CA367577302 | EGFR | c.469+1G>T (n.469+1G>T) n.818+1G>T c.628+1G>T (n.628+1G>T) c.493+1G>T (n.493+1G>T) c.89-4467G>T (n.89-4467G>T) | ClinVar dbSNP |
| 7 | g.55151364del | CA2682851569 | EGFR | c.469+2del (n.469+2del) n.818+2del c.628+2del (n.628+2del) c.493+2del (n.493+2del) c.89-4466del (n.89-4466del) | gnomAD v4 |
| 7 | g.55151364T>A | CA367577305 | EGFR | c.469+2T>A (n.469+2T>A) n.818+2T>A c.628+2T>A (n.628+2T>A) c.493+2T>A (n.493+2T>A) c.89-4466T>A (n.89-4466T>A) | dbSNP |
| 7 | g.55151364T>C | CA367577306 | EGFR | c.469+2T>C (n.469+2T>C) n.818+2T>C c.628+2T>C (n.628+2T>C) c.493+2T>C (n.493+2T>C) c.89-4466T>C (n.89-4466T>C) | |
| 7 | g.55151364T>G | CA367577307 | EGFR | c.469+2T>G (n.469+2T>G) n.818+2T>G c.628+2T>G (n.628+2T>G) c.493+2T>G (n.493+2T>G) c.89-4466T>G (n.89-4466T>G) | |
| 7 | g.55151364dup | CA2580077235 | EGFR | c.469+2dup (n.469+2dup) n.818+2dup c.628+2dup (n.628+2dup) c.493+2dup (n.493+2dup) c.89-4466dup (n.89-4466dup) | ClinVar |
| 7 | g.55151365A>G | CA2714936124 | EGFR | c.469+3A>G (n.469+3A>G) n.818+3A>G c.628+3A>G (n.628+3A>G) c.493+3A>G (n.493+3A>G) c.89-4465A>G (n.89-4465A>G) | ClinVar dbSNP |
| 7 | g.55151367G>C | CA2714936126 | EGFR | c.469+5G>C (n.469+5G>C) n.818+5G>C c.628+5G>C (n.628+5G>C) c.493+5G>C (n.493+5G>C) c.89-4463G>C (n.89-4463G>C) | dbSNP |
| 7 | g.55151368T>A | CA1708910452 | EGFR | c.469+6T>A (n.469+6T>A) n.818+6T>A c.628+6T>A (n.628+6T>A) c.493+6T>A (n.493+6T>A) c.89-4462T>A (n.89-4462T>A) | ClinVar dbSNP |
| 7 | g.55151368T= | CA1708910448 | EGFR | c.469+6T= (n.469+6T=) n.818+6T= c.628+6T= (n.628+6T=) c.493+6T= (n.493+6T=) c.89-4462T= (n.89-4462T=) | |
| 7 | g.55151369C>G | CA2714936359 | EGFR | c.469+7C>G (n.469+7C>G) n.818+7C>G c.628+7C>G (n.628+7C>G) c.493+7C>G (n.493+7C>G) c.89-4461C>G (n.89-4461C>G) | dbSNP |
| 7 | g.55151369C>T | CA2714936373 | EGFR | c.469+7C>T (n.469+7C>T) n.818+7C>T c.628+7C>T (n.628+7C>T) c.493+7C>T (n.493+7C>T) c.89-4461C>T (n.89-4461C>T) | dbSNP |
| 7 | g.55151371G>A | CA1708910459 | EGFR | c.469+9G>A (n.469+9G>A) n.818+9G>A c.628+9G>A (n.628+9G>A) c.493+9G>A (n.493+9G>A) c.89-4459G>A (n.89-4459G>A) | ClinVar dbSNP |
| 7 | g.55151371G>C | CA2714587087 | EGFR | c.469+9G>C (n.469+9G>C) n.818+9G>C c.628+9G>C (n.628+9G>C) c.493+9G>C (n.493+9G>C) c.89-4459G>C (n.89-4459G>C) | dbSNP |
| 7 | g.55151371G= | CA1708910457 | EGFR | c.469+9G= (n.469+9G=) n.818+9G= c.628+9G= (n.628+9G=) c.493+9G= (n.493+9G=) c.89-4459G= (n.89-4459G=) | |
| 7 | g.55151372T>A | CA2714936578 | EGFR | c.469+10T>A (n.469+10T>A) n.818+10T>A c.628+10T>A (n.628+10T>A) c.493+10T>A (n.493+10T>A) c.89-4458T>A (n.89-4458T>A) | dbSNP |
| 7 | g.55151372T>C | CA2580077237 | EGFR | c.469+10T>C (n.469+10T>C) n.818+10T>C c.628+10T>C (n.628+10T>C) c.493+10T>C (n.493+10T>C) c.89-4458T>C (n.89-4458T>C) | ClinVar gnomAD v4 |
| 7 | g.55151372T>G | CA2682851570 | EGFR | c.469+10T>G (n.469+10T>G) n.818+10T>G c.628+10T>G (n.628+10T>G) c.493+10T>G (n.493+10T>G) c.89-4458T>G (n.89-4458T>G) | ClinVar gnomAD v4 |
| 7 | g.55151373G>A | CA2714936583 | EGFR | c.469+11G>A (n.469+11G>A) n.818+11G>A c.628+11G>A (n.628+11G>A) c.493+11G>A (n.493+11G>A) c.89-4457G>A (n.89-4457G>A) | dbSNP |
| 7 | g.55151373G>C | CA2714936589 | EGFR | c.469+11G>C (n.469+11G>C) n.818+11G>C c.628+11G>C (n.628+11G>C) c.493+11G>C (n.493+11G>C) c.89-4457G>C (n.89-4457G>C) | dbSNP |