| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 7 | g.55201205T>A | CA367582371 | EGFR | c.2805T>A (p.His935Gln) c.900-4142T>A n.708T>A n.633T>A c.2964T>A (p.His988Gln) c.*28+28277T>A (n.*28+28277T>A) c.2829T>A (p.His943Gln) c.2163T>A (p.His721Gln) | dbSNP |
| 7 | g.55201205T>C | CA454968509 | EGFR | c.2805T>C (p.His935=) c.900-4142T>C n.708T>C n.633T>C c.2964T>C (p.His988=) c.*28+28277T>C (n.*28+28277T>C) c.2829T>C (p.His943=) c.2163T>C (p.His721=) | dbSNP |
| 7 | g.55201205T>G | CA367582372 | EGFR | c.2805T>G (p.His935Gln) c.900-4142T>G n.708T>G n.633T>G c.2964T>G (p.His988Gln) c.*28+28277T>G (n.*28+28277T>G) c.2829T>G (p.His943Gln) c.2163T>G (p.His721Gln) | |
| 7 | g.55201206T>A | CA367582373 | EGFR | c.2806T>A (p.Leu936Met) c.900-4141T>A n.709T>A n.634T>A c.2965T>A (p.Leu989Met) c.*28+28278T>A (n.*28+28278T>A) c.2830T>A (p.Leu944Met) c.2164T>A (p.Leu722Met) | dbSNP |
| 7 | g.55201206T>C | CA454968510 | EGFR | c.2806T>C (p.Leu936=) c.900-4141T>C n.709T>C n.634T>C c.2965T>C (p.Leu989=) c.*28+28278T>C (n.*28+28278T>C) c.2830T>C (p.Leu944=) c.2164T>C (p.Leu722=) | dbSNP |
| 7 | g.55201206T>G | CA367582374 | EGFR | c.2806T>G (p.Leu936Val) c.900-4141T>G n.709T>G n.634T>G c.2965T>G (p.Leu989Val) c.*28+28278T>G (n.*28+28278T>G) c.2830T>G (p.Leu944Val) c.2164T>G (p.Leu722Val) | |
| 7 | g.55201207T>A | CA367582375 | EGFR | c.2807T>A (p.Leu936Ter) c.900-4140T>A n.710T>A n.635T>A c.2966T>A (p.Leu989Ter) c.*28+28279T>A (n.*28+28279T>A) c.2831T>A (p.Leu944Ter) c.2165T>A (p.Leu722Ter) | dbSNP |
| 7 | g.55201207T>C | CA367582376 | EGFR | c.2807T>C (p.Leu936Ser) c.900-4140T>C n.710T>C n.635T>C c.2966T>C (p.Leu989Ser) c.*28+28279T>C (n.*28+28279T>C) c.2831T>C (p.Leu944Ser) c.2165T>C (p.Leu722Ser) | |
| 7 | g.55201207T>G | CA367582377 | EGFR | c.2807T>G (p.Leu936Trp) c.900-4140T>G n.710T>G n.635T>G c.2966T>G (p.Leu989Trp) c.*28+28279T>G (n.*28+28279T>G) c.2831T>G (p.Leu944Trp) c.2165T>G (p.Leu722Trp) | |
| 7 | g.55201208G>A | CA454968511 | EGFR | c.2808G>A (p.Leu936=) c.900-4139G>A n.711G>A n.636G>A c.2967G>A (p.Leu989=) c.*28+28280G>A (n.*28+28280G>A) c.2832G>A (p.Leu944=) c.2166G>A (p.Leu722=) | dbSNP |
| 7 | g.55201208G>C | CA367582378 | EGFR | c.2808G>C (p.Leu936Phe) c.900-4139G>C n.711G>C n.636G>C c.2967G>C (p.Leu989Phe) c.*28+28280G>C (n.*28+28280G>C) c.2832G>C (p.Leu944Phe) c.2166G>C (p.Leu722Phe) | dbSNP |
| 7 | g.55201208G>T | CA367582379 | EGFR | c.2808G>T (p.Leu936Phe) c.900-4139G>T n.711G>T n.636G>T c.2967G>T (p.Leu989Phe) c.*28+28280G>T (n.*28+28280G>T) c.2832G>T (p.Leu944Phe) c.2166G>T (p.Leu722Phe) | dbSNP |
| 7 | g.55201209C>A | CA367582380 | EGFR | c.2809C>A (p.Pro937Thr) c.900-4138C>A n.712C>A n.637C>A c.2968C>A (p.Pro990Thr) c.*28+28281C>A (n.*28+28281C>A) c.2833C>A (p.Pro945Thr) c.2167C>A (p.Pro723Thr) | dbSNP |
| 7 | g.55201209C= | CA1708928413 | EGFR | c.2809C= (p.Pro937=) c.900-4138C= n.712C= n.637C= c.2968C= (p.Pro990=) c.*28+28281C= (n.*28+28281C=) c.2833C= (p.Pro945=) c.2167C= (p.Pro723=) | |
| 7 | g.55201209C>G | CA367582381 | EGFR | c.2809C>G (p.Pro937Ala) c.900-4138C>G n.712C>G n.637C>G c.2968C>G (p.Pro990Ala) c.*28+28281C>G (n.*28+28281C>G) c.2833C>G (p.Pro945Ala) c.2167C>G (p.Pro723Ala) | dbSNP |
| 7 | g.55201209C>T | CA4266229 | EGFR | c.2809C>T (p.Pro937Ser) c.900-4138C>T n.712C>T n.637C>T c.2968C>T (p.Pro990Ser) c.*28+28281C>T (n.*28+28281C>T) c.2833C>T (p.Pro945Ser) c.2167C>T (p.Pro723Ser) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 7 | g.55201210C>A | CA367582383 | EGFR | c.2810C>A (p.Pro937Gln) c.900-4137C>A n.713C>A n.638C>A c.2969C>A (p.Pro990Gln) c.*28+28282C>A (n.*28+28282C>A) c.2834C>A (p.Pro945Gln) c.2168C>A (p.Pro723Gln) | dbSNP |
| 7 | g.55201210C>G | CA367582382 | EGFR | c.2810C>G (p.Pro937Arg) c.900-4137C>G n.713C>G n.638C>G c.2969C>G (p.Pro990Arg) c.*28+28282C>G (n.*28+28282C>G) c.2834C>G (p.Pro945Arg) c.2168C>G (p.Pro723Arg) | dbSNP gnomAD v4 |
| 7 | g.55201210C>T | CA367582384 | EGFR | c.2810C>T (p.Pro937Leu) c.900-4137C>T n.713C>T n.638C>T c.2969C>T (p.Pro990Leu) c.*28+28282C>T (n.*28+28282C>T) c.2834C>T (p.Pro945Leu) c.2168C>T (p.Pro723Leu) | dbSNP |
| 7 | g.55201211A>C | CA454968515 | EGFR | c.2811A>C (p.Pro937=) c.900-4136A>C n.714A>C n.639A>C c.2970A>C (p.Pro990=) c.*28+28283A>C (n.*28+28283A>C) c.2835A>C (p.Pro945=) c.2169A>C (p.Pro723=) | |
| 7 | g.55201211A>G | CA454968516 | EGFR | c.2811A>G (p.Pro937=) c.900-4136A>G n.714A>G n.639A>G c.2970A>G (p.Pro990=) c.*28+28283A>G (n.*28+28283A>G) c.2835A>G (p.Pro945=) c.2169A>G (p.Pro723=) | dbSNP |
| 7 | g.55201211A>T | CA454968517 | EGFR | c.2811A>T (p.Pro937=) c.900-4136A>T n.714A>T n.639A>T c.2970A>T (p.Pro990=) c.*28+28283A>T (n.*28+28283A>T) c.2835A>T (p.Pro945=) c.2169A>T (p.Pro723=) | dbSNP |
| 7 | g.55201212A= | CA1708928414 | EGFR | c.2812A= (p.Ser938=) c.900-4135A= n.715A= n.640A= c.2971A= (p.Ser991=) c.*28+28284A= (n.*28+28284A=) c.2836A= (p.Ser946=) c.2170A= (p.Ser724=) | |
| 7 | g.55201212A>C | CA4266231 | EGFR | c.2812A>C (p.Ser938Arg) c.900-4135A>C n.715A>C n.640A>C c.2971A>C (p.Ser991Arg) c.*28+28284A>C (n.*28+28284A>C) c.2836A>C (p.Ser946Arg) c.2170A>C (p.Ser724Arg) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 7 | g.55201212A>G | CA4266230 | EGFR | c.2812A>G (p.Ser938Gly) c.900-4135A>G n.715A>G n.640A>G c.2971A>G (p.Ser991Gly) c.*28+28284A>G (n.*28+28284A>G) c.2836A>G (p.Ser946Gly) c.2170A>G (p.Ser724Gly) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 7 | g.55201212A>T | CA367582385 | EGFR | c.2812A>T (p.Ser938Cys) c.900-4135A>T n.715A>T n.640A>T c.2971A>T (p.Ser991Cys) c.*28+28284A>T (n.*28+28284A>T) c.2836A>T (p.Ser946Cys) c.2170A>T (p.Ser724Cys) | |
| 7 | g.55201213G>A | CA367582386 | EGFR | c.2813G>A (p.Ser938Asn) c.900-4134G>A n.716G>A n.641G>A c.2972G>A (p.Ser991Asn) c.*28+28285G>A (n.*28+28285G>A) c.2837G>A (p.Ser946Asn) c.2171G>A (p.Ser724Asn) | ClinVar dbSNP gnomAD v4 |
| 7 | g.55201213G>C | CA367582387 | EGFR | c.2813G>C (p.Ser938Thr) c.900-4134G>C n.716G>C n.641G>C c.2972G>C (p.Ser991Thr) c.*28+28285G>C (n.*28+28285G>C) c.2837G>C (p.Ser946Thr) c.2171G>C (p.Ser724Thr) | ClinVar dbSNP |
| 7 | g.55201213G= | CA1708928415 | EGFR | c.2813G= (p.Ser938=) c.900-4134G= n.716G= n.641G= c.2972G= (p.Ser991=) c.*28+28285G= (n.*28+28285G=) c.2837G= (p.Ser946=) c.2171G= (p.Ser724=) | |
| 7 | g.55201213G>T | CA367582388 | EGFR | c.2813G>T (p.Ser938Ile) c.900-4134G>T n.716G>T n.641G>T c.2972G>T (p.Ser991Ile) c.*28+28285G>T (n.*28+28285G>T) c.2837G>T (p.Ser946Ile) c.2171G>T (p.Ser724Ile) | |
| 7 | g.55201214T>A | CA367582390 | EGFR | c.2814T>A (p.Ser938Arg) c.900-4133T>A n.717T>A n.642T>A c.2973T>A (p.Ser991Arg) c.*28+28286T>A (n.*28+28286T>A) c.2838T>A (p.Ser946Arg) c.2172T>A (p.Ser724Arg) | dbSNP |
| 7 | g.55201214T>C | CA454968520 | EGFR | c.2814T>C (p.Ser938=) c.900-4133T>C n.717T>C n.642T>C c.2973T>C (p.Ser991=) c.*28+28286T>C (n.*28+28286T>C) c.2838T>C (p.Ser946=) c.2172T>C (p.Ser724=) | dbSNP |
| 7 | g.55201214T>G | CA367582389 | EGFR | c.2814T>G (p.Ser938Arg) c.900-4133T>G n.717T>G n.642T>G c.2973T>G (p.Ser991Arg) c.*28+28286T>G (n.*28+28286T>G) c.2838T>G (p.Ser946Arg) c.2172T>G (p.Ser724Arg) | dbSNP |
| 7 | g.55201215C>A | CA367582391 | EGFR | c.2815C>A (p.Pro939Thr) c.900-4132C>A n.718C>A n.643C>A c.2974C>A (p.Pro992Thr) c.*28+28287C>A (n.*28+28287C>A) c.2839C>A (p.Pro947Thr) c.2173C>A (p.Pro725Thr) | dbSNP |
| 7 | g.55201215C>G | CA367582392 | EGFR | c.2815C>G (p.Pro939Ala) c.900-4132C>G n.718C>G n.643C>G c.2974C>G (p.Pro992Ala) c.*28+28287C>G (n.*28+28287C>G) c.2839C>G (p.Pro947Ala) c.2173C>G (p.Pro725Ala) | dbSNP |
| 7 | g.55201215C>T | CA367582393 | EGFR | c.2815C>T (p.Pro939Ser) c.900-4132C>T n.718C>T n.643C>T c.2974C>T (p.Pro992Ser) c.*28+28287C>T (n.*28+28287C>T) c.2839C>T (p.Pro947Ser) c.2173C>T (p.Pro725Ser) | dbSNP |
| 7 | g.55201216C>A | CA367582394 | EGFR | c.2816C>A (p.Pro939His) c.900-4131C>A n.719C>A n.644C>A c.2975C>A (p.Pro992His) c.*28+28288C>A (n.*28+28288C>A) c.2840C>A (p.Pro947His) c.2174C>A (p.Pro725His) | dbSNP |
| 7 | g.55201216C>G | CA367582395 | EGFR | c.2816C>G (p.Pro939Arg) c.900-4131C>G n.719C>G n.644C>G c.2975C>G (p.Pro992Arg) c.*28+28288C>G (n.*28+28288C>G) c.2840C>G (p.Pro947Arg) c.2174C>G (p.Pro725Arg) | dbSNP |
| 7 | g.55201216C>T | CA367582396 | EGFR | c.2816C>T (p.Pro939Leu) c.900-4131C>T n.719C>T n.644C>T c.2975C>T (p.Pro992Leu) c.*28+28288C>T (n.*28+28288C>T) c.2840C>T (p.Pro947Leu) c.2174C>T (p.Pro725Leu) | dbSNP |
| 7 | g.55201217T>A | CA454968523 | EGFR | c.2817T>A (p.Pro939=) c.900-4130T>A n.720T>A n.645T>A c.2976T>A (p.Pro992=) c.*28+28289T>A (n.*28+28289T>A) c.2841T>A (p.Pro947=) c.2175T>A (p.Pro725=) | |
| 7 | g.55201217T>C | CA454968524 | EGFR | c.2817T>C (p.Pro939=) c.900-4130T>C n.720T>C n.645T>C c.2976T>C (p.Pro992=) c.*28+28289T>C (n.*28+28289T>C) c.2841T>C (p.Pro947=) c.2175T>C (p.Pro725=) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 7 | g.55201217T>G | CA454968522 | EGFR | c.2817T>G (p.Pro939=) c.900-4130T>G n.720T>G n.645T>G c.2976T>G (p.Pro992=) c.*28+28289T>G (n.*28+28289T>G) c.2841T>G (p.Pro947=) c.2175T>G (p.Pro725=) | ClinVar |
| 7 | g.55201217T= | CA1708928416 | EGFR | c.2817T= (p.Pro939=) c.900-4130T= n.720T= n.645T= c.2976T= (p.Pro992=) c.*28+28289T= (n.*28+28289T=) c.2841T= (p.Pro947=) c.2175T= (p.Pro725=) | |
| 7 | g.55201218A>C | CA367582397 | EGFR | c.2818A>C (p.Thr940Pro) c.900-4129A>C n.721A>C n.646A>C c.2977A>C (p.Thr993Pro) c.*28+28290A>C (n.*28+28290A>C) c.2842A>C (p.Thr948Pro) c.2176A>C (p.Thr726Pro) | ClinVar dbSNP |
| 7 | g.55201218A>G | CA367582399 | EGFR | c.2818A>G (p.Thr940Ala) c.900-4129A>G n.721A>G n.646A>G c.2977A>G (p.Thr993Ala) c.*28+28290A>G (n.*28+28290A>G) c.2842A>G (p.Thr948Ala) c.2176A>G (p.Thr726Ala) | ClinVar dbSNP gnomAD v4 |
| 7 | g.55201218A>T | CA367582398 | EGFR | c.2818A>T (p.Thr940Ser) c.900-4129A>T n.721A>T n.646A>T c.2977A>T (p.Thr993Ser) c.*28+28290A>T (n.*28+28290A>T) c.2842A>T (p.Thr948Ser) c.2176A>T (p.Thr726Ser) | dbSNP |
| 7 | g.55201219C>A | CA367582400 | EGFR | c.2819C>A (p.Thr940Lys) c.900-4128C>A n.722C>A n.647C>A c.2978C>A (p.Thr993Lys) c.*28+28291C>A (n.*28+28291C>A) c.2843C>A (p.Thr948Lys) c.2177C>A (p.Thr726Lys) | dbSNP |
| 7 | g.55201219C>G | CA367582401 | EGFR | c.2819C>G (p.Thr940Arg) c.900-4128C>G n.722C>G n.647C>G c.2978C>G (p.Thr993Arg) c.*28+28291C>G (n.*28+28291C>G) c.2843C>G (p.Thr948Arg) c.2177C>G (p.Thr726Arg) | dbSNP |
| 7 | g.55201219C>T | CA367582402 | EGFR | c.2819C>T (p.Thr940Ile) c.900-4128C>T n.722C>T n.647C>T c.2978C>T (p.Thr993Ile) c.*28+28291C>T (n.*28+28291C>T) c.2843C>T (p.Thr948Ile) c.2177C>T (p.Thr726Ile) | ClinVar dbSNP gnomAD v4 |
| 7 | g.55201220A>C | CA454968527 | EGFR | c.2820A>C (p.Thr940=) c.900-4127A>C n.723A>C n.648A>C c.2979A>C (p.Thr993=) c.*28+28292A>C (n.*28+28292A>C) c.2844A>C (p.Thr948=) c.2178A>C (p.Thr726=) | |
| 7 | g.55201220A>G | CA454968528 | EGFR | c.2820A>G (p.Thr940=) c.900-4127A>G n.723A>G n.648A>G c.2979A>G (p.Thr993=) c.*28+28292A>G (n.*28+28292A>G) c.2844A>G (p.Thr948=) c.2178A>G (p.Thr726=) | |
| 7 | g.55201220A>T | CA454968529 | EGFR | c.2820A>T (p.Thr940=) c.900-4127A>T n.723A>T n.648A>T c.2979A>T (p.Thr993=) c.*28+28292A>T (n.*28+28292A>T) c.2844A>T (p.Thr948=) c.2178A>T (p.Thr726=) | dbSNP |
| 7 | g.55201221G>A | CA367582403 | EGFR | c.2821G>A (p.Asp941Asn) c.900-4126G>A n.724G>A n.649G>A c.2980G>A (p.Asp994Asn) c.*28+28293G>A (n.*28+28293G>A) c.2845G>A (p.Asp949Asn) c.2179G>A (p.Asp727Asn) | ClinVar dbSNP gnomAD v4 |
| 7 | g.55201221G>C | CA367582404 | EGFR | c.2821G>C (p.Asp941His) c.900-4126G>C n.724G>C n.649G>C c.2980G>C (p.Asp994His) c.*28+28293G>C (n.*28+28293G>C) c.2845G>C (p.Asp949His) c.2179G>C (p.Asp727His) | |
| 7 | g.55201221G= | CA1708928417 | EGFR | c.2821G= (p.Asp941=) c.900-4126G= n.724G= n.649G= c.2980G= (p.Asp994=) c.*28+28293G= (n.*28+28293G=) c.2845G= (p.Asp949=) c.2179G= (p.Asp727=) | |
| 7 | g.55201221G>T | CA367582405 | EGFR | c.2821G>T (p.Asp941Tyr) c.900-4126G>T n.724G>T n.649G>T c.2980G>T (p.Asp994Tyr) c.*28+28293G>T (n.*28+28293G>T) c.2845G>T (p.Asp949Tyr) c.2179G>T (p.Asp727Tyr) | |
| 7 | g.55201222A>C | CA367582406 | EGFR | c.2822A>C (p.Asp941Ala) c.900-4125A>C n.725A>C n.650A>C c.2981A>C (p.Asp994Ala) c.*28+28294A>C (n.*28+28294A>C) c.2846A>C (p.Asp949Ala) c.2180A>C (p.Asp727Ala) | ClinVar dbSNP |
| 7 | g.55201222A>G | CA367582407 | EGFR | c.2822A>G (p.Asp941Gly) c.900-4125A>G n.725A>G n.650A>G c.2981A>G (p.Asp994Gly) c.*28+28294A>G (n.*28+28294A>G) c.2846A>G (p.Asp949Gly) c.2180A>G (p.Asp727Gly) | dbSNP |
| 7 | g.55201222A>T | CA367582408 | EGFR | c.2822A>T (p.Asp941Val) c.900-4125A>T n.725A>T n.650A>T c.2981A>T (p.Asp994Val) c.*28+28294A>T (n.*28+28294A>T) c.2846A>T (p.Asp949Val) c.2180A>T (p.Asp727Val) | dbSNP |
| 7 | g.55201222_55201224delinsACT | CA1708928418 | EGFR | c.2822_2824delinsACT (p.Asp941=) c.900-4125_900-4123delinsACT n.725_727delinsACT n.650_652delinsACT c.2981_2983delinsACT (p.Asp994=) c.*28+28294_*28+28296delinsACT (n.*28+28294_*28+28296delinsACT) c.2846_2848delinsACT (p.Asp949=) c.2180_2182delinsACT (p.Asp727=) | |
| 7 | g.55201222_55201224delinsGTG | CA158462 | EGFR | c.2822_2824delinsGTG (p.Asp941_Ser942delinsGlyAla) c.900-4125_900-4123delinsGTG n.725_727delinsGTG n.650_652delinsGTG c.2981_2983delinsGTG (p.Asp994_Ser995delinsGlyAla) c.*28+28294_*28+28296delinsGTG (n.*28+28294_*28+28296delinsGTG) c.2846_2848delinsGTG (p.Asp949_Ser950delinsGlyAla) c.2180_2182delinsGTG (p.Asp727_Ser728delinsGlyAla) | ClinVar dbSNP |
| 7 | g.55201223C>A | CA367582410 | EGFR | c.2823C>A (p.Asp941Glu) c.900-4124C>A n.726C>A n.651C>A c.2982C>A (p.Asp994Glu) c.*28+28295C>A (n.*28+28295C>A) c.2847C>A (p.Asp949Glu) c.2181C>A (p.Asp727Glu) | |
| 7 | g.55201223C= | CA1708928419 | EGFR | c.2823C= (p.Asp941=) c.900-4124C= n.726C= n.651C= c.2982C= (p.Asp994=) c.*28+28295C= (n.*28+28295C=) c.2847C= (p.Asp949=) c.2181C= (p.Asp727=) | |
| 7 | g.55201223C>G | CA367582409 | EGFR | c.2823C>G (p.Asp941Glu) c.900-4124C>G n.726C>G n.651C>G c.2982C>G (p.Asp994Glu) c.*28+28295C>G (n.*28+28295C>G) c.2847C>G (p.Asp949Glu) c.2181C>G (p.Asp727Glu) | dbSNP |
| 7 | g.55201223C>T | CA4266232 | EGFR | c.2823C>T (p.Asp941=) c.900-4124C>T n.726C>T n.651C>T c.2982C>T (p.Asp994=) c.*28+28295C>T (n.*28+28295C>T) c.2847C>T (p.Asp949=) c.2181C>T (p.Asp727=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 7 | g.55201224T>A | CA367582411 | EGFR | c.2824T>A (p.Ser942Thr) c.900-4123T>A n.727T>A n.652T>A c.2983T>A (p.Ser995Thr) c.*28+28296T>A (n.*28+28296T>A) c.2848T>A (p.Ser950Thr) c.2182T>A (p.Ser728Thr) | ClinVar dbSNP gnomAD v4 |
| 7 | g.55201224T>C | CA367582412 | EGFR | c.2824T>C (p.Ser942Pro) c.900-4123T>C n.727T>C n.652T>C c.2983T>C (p.Ser995Pro) c.*28+28296T>C (n.*28+28296T>C) c.2848T>C (p.Ser950Pro) c.2182T>C (p.Ser728Pro) | ClinVar dbSNP |
| 7 | g.55201224T>G | CA367582413 | EGFR | c.2824T>G (p.Ser942Ala) c.900-4123T>G n.727T>G n.652T>G c.2983T>G (p.Ser995Ala) c.*28+28296T>G (n.*28+28296T>G) c.2848T>G (p.Ser950Ala) c.2182T>G (p.Ser728Ala) | |
| 7 | g.55201225C>A | CA367582414 | EGFR | c.2825C>A (p.Ser942Tyr) c.900-4122C>A n.728C>A n.653C>A c.2984C>A (p.Ser995Tyr) c.*28+28297C>A (n.*28+28297C>A) c.2849C>A (p.Ser950Tyr) c.2183C>A (p.Ser728Tyr) | |
| 7 | g.55201225C= | CA1708928420 | EGFR | c.2825C= (p.Ser942=) c.900-4122C= n.728C= n.653C= c.2984C= (p.Ser995=) c.*28+28297C= (n.*28+28297C=) c.2849C= (p.Ser950=) c.2183C= (p.Ser728=) | |
| 7 | g.55201225C>G | CA158937832 | EGFR | c.2825C>G (p.Ser942Cys) c.900-4122C>G n.728C>G n.653C>G c.2984C>G (p.Ser995Cys) c.*28+28297C>G (n.*28+28297C>G) c.2849C>G (p.Ser950Cys) c.2183C>G (p.Ser728Cys) | dbSNP |
| 7 | g.55201225C>T | CA367582415 | EGFR | c.2825C>T (p.Ser942Phe) c.900-4122C>T n.728C>T n.653C>T c.2984C>T (p.Ser995Phe) c.*28+28297C>T (n.*28+28297C>T) c.2849C>T (p.Ser950Phe) c.2183C>T (p.Ser728Phe) | gnomAD v4 |
| 7 | g.55201226C>A | CA454968530 | EGFR | c.2826C>A (p.Ser942=) c.900-4121C>A n.729C>A n.654C>A c.2985C>A (p.Ser995=) c.*28+28298C>A (n.*28+28298C>A) c.2850C>A (p.Ser950=) c.2184C>A (p.Ser728=) | dbSNP |
| 7 | g.55201226C>G | CA454968531 | EGFR | c.2826C>G (p.Ser942=) c.900-4121C>G n.729C>G n.654C>G c.2985C>G (p.Ser995=) c.*28+28298C>G (n.*28+28298C>G) c.2850C>G (p.Ser950=) c.2184C>G (p.Ser728=) | dbSNP |
| 7 | g.55201226C>T | CA454968532 | EGFR | c.2826C>T (p.Ser942=) c.900-4121C>T n.729C>T n.654C>T c.2985C>T (p.Ser995=) c.*28+28298C>T (n.*28+28298C>T) c.2850C>T (p.Ser950=) c.2184C>T (p.Ser728=) | dbSNP |
| 7 | g.55201227A>C | CA367582418 | EGFR | c.2827A>C (p.Asn943His) c.900-4120A>C n.730A>C n.655A>C c.2986A>C (p.Asn996His) c.*28+28299A>C (n.*28+28299A>C) c.2851A>C (p.Asn951His) c.2185A>C (p.Asn729His) | |
| 7 | g.55201227A>G | CA367582416 | EGFR | c.2827A>G (p.Asn943Asp) c.900-4120A>G n.730A>G n.655A>G c.2986A>G (p.Asn996Asp) c.*28+28299A>G (n.*28+28299A>G) c.2851A>G (p.Asn951Asp) c.2185A>G (p.Asn729Asp) | dbSNP |
| 7 | g.55201227A>T | CA367582417 | EGFR | c.2827A>T (p.Asn943Tyr) c.900-4120A>T n.730A>T n.655A>T c.2986A>T (p.Asn996Tyr) c.*28+28299A>T (n.*28+28299A>T) c.2851A>T (p.Asn951Tyr) c.2185A>T (p.Asn729Tyr) | dbSNP |
| 7 | g.55201228A= | CA1708928421 | EGFR | c.2828A= (p.Asn943=) c.900-4119A= n.731A= n.656A= c.2987A= (p.Asn996=) c.*28+28300A= (n.*28+28300A=) c.2852A= (p.Asn951=) c.2186A= (p.Asn729=) | |
| 7 | g.55201228A>C | CA367582419 | EGFR | c.2828A>C (p.Asn943Thr) c.900-4119A>C n.731A>C n.656A>C c.2987A>C (p.Asn996Thr) c.*28+28300A>C (n.*28+28300A>C) c.2852A>C (p.Asn951Thr) c.2186A>C (p.Asn729Thr) | dbSNP |
| 7 | g.55201228A>G | CA4266233 | EGFR | c.2828A>G (p.Asn943Ser) c.900-4119A>G n.731A>G n.656A>G c.2987A>G (p.Asn996Ser) c.*28+28300A>G (n.*28+28300A>G) c.2852A>G (p.Asn951Ser) c.2186A>G (p.Asn729Ser) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 7 | g.55201228A>T | CA367582420 | EGFR | c.2828A>T (p.Asn943Ile) c.900-4119A>T n.731A>T n.656A>T c.2987A>T (p.Asn996Ile) c.*28+28300A>T (n.*28+28300A>T) c.2852A>T (p.Asn951Ile) c.2186A>T (p.Asn729Ile) | dbSNP |
| 7 | g.55201229C>A | CA4266234 | EGFR | c.2829C>A (p.Asn943Lys) c.900-4118C>A n.732C>A n.657C>A c.2988C>A (p.Asn996Lys) c.*28+28301C>A (n.*28+28301C>A) c.2853C>A (p.Asn951Lys) c.2187C>A (p.Asn729Lys) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 7 | g.55201229C= | CA1708928422 | EGFR | c.2829C= (p.Asn943=) c.900-4118C= n.732C= n.657C= c.2988C= (p.Asn996=) c.*28+28301C= (n.*28+28301C=) c.2853C= (p.Asn951=) c.2187C= (p.Asn729=) | |
| 7 | g.55201229C>G | CA367582421 | EGFR | c.2829C>G (p.Asn943Lys) c.900-4118C>G n.732C>G n.657C>G c.2988C>G (p.Asn996Lys) c.*28+28301C>G (n.*28+28301C>G) c.2853C>G (p.Asn951Lys) c.2187C>G (p.Asn729Lys) | dbSNP |
| 7 | g.55201229C>T | CA454968535 | EGFR | c.2829C>T (p.Asn943=) c.900-4118C>T n.732C>T n.657C>T c.2988C>T (p.Asn996=) c.*28+28301C>T (n.*28+28301C>T) c.2853C>T (p.Asn951=) c.2187C>T (p.Asn729=) | ClinVar dbSNP gnomAD v4 |
| 7 | g.55201230T>A | CA367582422 | EGFR | c.2830T>A (p.Phe944Ile) c.900-4117T>A n.733T>A n.658T>A c.2989T>A (p.Phe997Ile) c.*28+28302T>A (n.*28+28302T>A) c.2854T>A (p.Phe952Ile) c.2188T>A (p.Phe730Ile) | dbSNP |
| 7 | g.55201230T>C | CA367582424 | EGFR | c.2830T>C (p.Phe944Leu) c.900-4117T>C n.733T>C n.658T>C c.2989T>C (p.Phe997Leu) c.*28+28302T>C (n.*28+28302T>C) c.2854T>C (p.Phe952Leu) c.2188T>C (p.Phe730Leu) | |
| 7 | g.55201230T>G | CA367582423 | EGFR | c.2830T>G (p.Phe944Val) c.900-4117T>G n.733T>G n.658T>G c.2989T>G (p.Phe997Val) c.*28+28302T>G (n.*28+28302T>G) c.2854T>G (p.Phe952Val) c.2188T>G (p.Phe730Val) | COSMIC |
| 7 | g.55201231T>A | CA367582425 | EGFR | c.2831T>A (p.Phe944Tyr) c.900-4116T>A n.734T>A n.659T>A c.2990T>A (p.Phe997Tyr) c.*28+28303T>A (n.*28+28303T>A) c.2855T>A (p.Phe952Tyr) c.2189T>A (p.Phe730Tyr) | dbSNP |
| 7 | g.55201231T>C | CA367582426 | EGFR | c.2831T>C (p.Phe944Ser) c.900-4116T>C n.734T>C n.659T>C c.2990T>C (p.Phe997Ser) c.*28+28303T>C (n.*28+28303T>C) c.2855T>C (p.Phe952Ser) c.2189T>C (p.Phe730Ser) | |
| 7 | g.55201231T>G | CA367582427 | EGFR | c.2831T>G (p.Phe944Cys) c.900-4116T>G n.734T>G n.659T>G c.2990T>G (p.Phe997Cys) c.*28+28303T>G (n.*28+28303T>G) c.2855T>G (p.Phe952Cys) c.2189T>G (p.Phe730Cys) | |
| 7 | g.55201232C>A | CA367582428 | EGFR | c.2832C>A (p.Phe944Leu) c.900-4115C>A n.735C>A n.660C>A c.2991C>A (p.Phe997Leu) c.*28+28304C>A (n.*28+28304C>A) c.2856C>A (p.Phe952Leu) c.2190C>A (p.Phe730Leu) | dbSNP |
| 7 | g.55201232C>G | CA367582429 | EGFR | c.2832C>G (p.Phe944Leu) c.900-4115C>G n.735C>G n.660C>G c.2991C>G (p.Phe997Leu) c.*28+28304C>G (n.*28+28304C>G) c.2856C>G (p.Phe952Leu) c.2190C>G (p.Phe730Leu) | dbSNP |
| 7 | g.55201232C>T | CA454968536 | EGFR | c.2832C>T (p.Phe944=) c.900-4115C>T n.735C>T n.660C>T c.2991C>T (p.Phe997=) c.*28+28304C>T (n.*28+28304C>T) c.2856C>T (p.Phe952=) c.2190C>T (p.Phe730=) | dbSNP gnomAD v4 COSMIC |
| 7 | g.55201233T>A | CA367582430 | EGFR | c.2833T>A (p.Tyr945Asn) c.900-4114T>A n.736T>A n.661T>A c.2992T>A (p.Tyr998Asn) c.*28+28305T>A (n.*28+28305T>A) c.2857T>A (p.Tyr953Asn) c.2191T>A (p.Tyr731Asn) | dbSNP |
| 7 | g.55201233T>C | CA367582431 | EGFR | c.2833T>C (p.Tyr945His) c.900-4114T>C n.736T>C n.661T>C c.2992T>C (p.Tyr998His) c.*28+28305T>C (n.*28+28305T>C) c.2857T>C (p.Tyr953His) c.2191T>C (p.Tyr731His) | dbSNP gnomAD v4 |
| 7 | g.55201233T>G | CA367582432 | EGFR | c.2833T>G (p.Tyr945Asp) c.900-4114T>G n.736T>G n.661T>G c.2992T>G (p.Tyr998Asp) c.*28+28305T>G (n.*28+28305T>G) c.2857T>G (p.Tyr953Asp) c.2191T>G (p.Tyr731Asp) | |
| 7 | g.55201234A= | CA1708928423 | EGFR | c.2834A= (p.Tyr945=) c.900-4113A= n.737A= n.662A= c.2993A= (p.Tyr998=) c.*28+28306A= (n.*28+28306A=) c.2858A= (p.Tyr953=) c.2192A= (p.Tyr731=) | |
| 7 | g.55201234A>C | CA367582433 | EGFR | c.2834A>C (p.Tyr945Ser) c.900-4113A>C n.737A>C n.662A>C c.2993A>C (p.Tyr998Ser) c.*28+28306A>C (n.*28+28306A>C) c.2858A>C (p.Tyr953Ser) c.2192A>C (p.Tyr731Ser) | dbSNP |
| 7 | g.55201234A>G | CA367582434 | EGFR | c.2834A>G (p.Tyr945Cys) c.900-4113A>G n.737A>G n.662A>G c.2993A>G (p.Tyr998Cys) c.*28+28306A>G (n.*28+28306A>G) c.2858A>G (p.Tyr953Cys) c.2192A>G (p.Tyr731Cys) | ClinVar dbSNP |
| 7 | g.55201234A>T | CA367582435 | EGFR | c.2834A>T (p.Tyr945Phe) c.900-4113A>T n.737A>T n.662A>T c.2993A>T (p.Tyr998Phe) c.*28+28306A>T (n.*28+28306A>T) c.2858A>T (p.Tyr953Phe) c.2192A>T (p.Tyr731Phe) | dbSNP |
| 7 | g.55201235C>A | CA367582437 | EGFR | c.2835C>A (p.Tyr945Ter) c.900-4112C>A n.738C>A n.663C>A c.2994C>A (p.Tyr998Ter) c.*28+28307C>A (n.*28+28307C>A) c.2859C>A (p.Tyr953Ter) c.2193C>A (p.Tyr731Ter) | dbSNP |
| 7 | g.55201235C= | CA1708928424 | EGFR | c.2835C= (p.Tyr945=) c.900-4112C= n.738C= n.663C= c.2994C= (p.Tyr998=) c.*28+28307C= (n.*28+28307C=) c.2859C= (p.Tyr953=) c.2193C= (p.Tyr731=) | |
| 7 | g.55201235C>G | CA367582436 | EGFR | c.2835C>G (p.Tyr945Ter) c.900-4112C>G n.738C>G n.663C>G c.2994C>G (p.Tyr998Ter) c.*28+28307C>G (n.*28+28307C>G) c.2859C>G (p.Tyr953Ter) c.2193C>G (p.Tyr731Ter) | dbSNP |
| 7 | g.55201235C>T | CA454968538 | EGFR | c.2835C>T (p.Tyr945=) c.900-4112C>T n.738C>T n.663C>T c.2994C>T (p.Tyr998=) c.*28+28307C>T (n.*28+28307C>T) c.2859C>T (p.Tyr953=) c.2193C>T (p.Tyr731=) | ClinVar dbSNP |
| 7 | g.55201236C>A | CA367582438 | EGFR | c.2836C>A (p.Arg946Ser) c.900-4111C>A n.739C>A n.664C>A c.2995C>A (p.Arg999Ser) c.*28+28308C>A (n.*28+28308C>A) c.2860C>A (p.Arg954Ser) c.2194C>A (p.Arg732Ser) | dbSNP |
| 7 | g.55201236C= | CA1708928425 | EGFR | c.2836C= (p.Arg946=) c.900-4111C= n.739C= n.664C= c.2995C= (p.Arg999=) c.*28+28308C= (n.*28+28308C=) c.2860C= (p.Arg954=) c.2194C= (p.Arg732=) | |
| 7 | g.55201236C>G | CA367582439 | EGFR | c.2836C>G (p.Arg946Gly) c.900-4111C>G n.739C>G n.664C>G c.2995C>G (p.Arg999Gly) c.*28+28308C>G (n.*28+28308C>G) c.2860C>G (p.Arg954Gly) c.2194C>G (p.Arg732Gly) | dbSNP |
| 7 | g.55201236C>T | CA158937840 | EGFR | c.2836C>T (p.Arg946Cys) c.900-4111C>T n.739C>T n.664C>T c.2995C>T (p.Arg999Cys) c.*28+28308C>T (n.*28+28308C>T) c.2860C>T (p.Arg954Cys) c.2194C>T (p.Arg732Cys) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 7 | g.55201237G>A | CA4266235 | EGFR | c.2837G>A (p.Arg946His) c.900-4110G>A n.740G>A n.665G>A c.2996G>A (p.Arg999His) c.*28+28309G>A (n.*28+28309G>A) c.2861G>A (p.Arg954His) c.2195G>A (p.Arg732His) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 7 | g.55201237G>C | CA367582440 | EGFR | c.2837G>C (p.Arg946Pro) c.900-4110G>C n.740G>C n.665G>C c.2996G>C (p.Arg999Pro) c.*28+28309G>C (n.*28+28309G>C) c.2861G>C (p.Arg954Pro) c.2195G>C (p.Arg732Pro) | dbSNP |
| 7 | g.55201237G= | CA1708928426 | EGFR | c.2837G= (p.Arg946=) c.900-4110G= n.740G= n.665G= c.2996G= (p.Arg999=) c.*28+28309G= (n.*28+28309G=) c.2861G= (p.Arg954=) c.2195G= (p.Arg732=) | |
| 7 | g.55201237G>T | CA10624139 | EGFR | c.2837G>T (p.Arg946Leu) c.900-4110G>T n.740G>T n.665G>T c.2996G>T (p.Arg999Leu) c.*28+28309G>T (n.*28+28309G>T) c.2861G>T (p.Arg954Leu) c.2195G>T (p.Arg732Leu) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 7 | g.55201238T>A | CA454968542 | EGFR | c.2838T>A (p.Arg946=) c.900-4109T>A n.741T>A n.666T>A c.2997T>A (p.Arg999=) c.*28+28310T>A (n.*28+28310T>A) c.2862T>A (p.Arg954=) c.2196T>A (p.Arg732=) | dbSNP |
| 7 | g.55201238T>C | CA4266236 | EGFR | c.2838T>C (p.Arg946=) c.900-4109T>C n.741T>C n.666T>C c.2997T>C (p.Arg999=) c.*28+28310T>C (n.*28+28310T>C) c.2862T>C (p.Arg954=) c.2196T>C (p.Arg732=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 7 | g.55201238T>G | CA454968540 | EGFR | c.2838T>G (p.Arg946=) c.900-4109T>G n.741T>G n.666T>G c.2997T>G (p.Arg999=) c.*28+28310T>G (n.*28+28310T>G) c.2862T>G (p.Arg954=) c.2196T>G (p.Arg732=) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 7 | g.55201238T= | CA1708928427 | EGFR | c.2838T= (p.Arg946=) c.900-4109T= n.741T= n.666T= c.2997T= (p.Arg999=) c.*28+28310T= (n.*28+28310T=) c.2862T= (p.Arg954=) c.2196T= (p.Arg732=) | |
| 7 | g.55201239G>A | CA367582441 | EGFR | c.2839G>A (p.Ala947Thr) c.900-4108G>A n.742G>A n.667G>A c.2998G>A (p.Ala1000Thr) c.*28+28311G>A (n.*28+28311G>A) c.2863G>A (p.Ala955Thr) c.2197G>A (p.Ala733Thr) | ClinVar dbSNP gnomAD v4 |
| 7 | g.55201239G>C | CA367582442 | EGFR | c.2839G>C (p.Ala947Pro) c.900-4108G>C n.742G>C n.667G>C c.2998G>C (p.Ala1000Pro) c.*28+28311G>C (n.*28+28311G>C) c.2863G>C (p.Ala955Pro) c.2197G>C (p.Ala733Pro) | dbSNP |
| 7 | g.55201239G>T | CA367582443 | EGFR | c.2839G>T (p.Ala947Ser) c.900-4108G>T n.742G>T n.667G>T c.2998G>T (p.Ala1000Ser) c.*28+28311G>T (n.*28+28311G>T) c.2863G>T (p.Ala955Ser) c.2197G>T (p.Ala733Ser) | dbSNP |
| 7 | g.55201240C>A | CA367582444 | EGFR | c.2840C>A (p.Ala947Asp) c.900-4107C>A n.743C>A n.668C>A c.2999C>A (p.Ala1000Asp) c.*28+28312C>A (n.*28+28312C>A) c.2864C>A (p.Ala955Asp) c.2198C>A (p.Ala733Asp) | ClinVar dbSNP |
| 7 | g.55201240C= | CA1708928428 | EGFR | c.2840C= (p.Ala947=) c.900-4107C= n.743C= n.668C= c.2999C= (p.Ala1000=) c.*28+28312C= (n.*28+28312C=) c.2864C= (p.Ala955=) c.2198C= (p.Ala733=) | |
| 7 | g.55201240C>G | CA367582445 | EGFR | c.2840C>G (p.Ala947Gly) c.900-4107C>G n.743C>G n.668C>G c.2999C>G (p.Ala1000Gly) c.*28+28312C>G (n.*28+28312C>G) c.2864C>G (p.Ala955Gly) c.2198C>G (p.Ala733Gly) | dbSNP |
| 7 | g.55201240C>T | CA367582446 | EGFR | c.2840C>T (p.Ala947Val) c.900-4107C>T n.743C>T n.668C>T c.2999C>T (p.Ala1000Val) c.*28+28312C>T (n.*28+28312C>T) c.2864C>T (p.Ala955Val) c.2198C>T (p.Ala733Val) | dbSNP gnomAD v4 |
| 7 | g.55201241C>A | CA454968546 | EGFR | c.2841C>A (p.Ala947=) c.900-4106C>A n.744C>A n.669C>A c.3000C>A (p.Ala1000=) c.*28+28313C>A (n.*28+28313C>A) c.2865C>A (p.Ala955=) c.2199C>A (p.Ala733=) | dbSNP |
| 7 | g.55201241C= | CA1708928429 | EGFR | c.2841C= (p.Ala947=) c.900-4106C= n.744C= n.669C= c.3000C= (p.Ala1000=) c.*28+28313C= (n.*28+28313C=) c.2865C= (p.Ala955=) c.2199C= (p.Ala733=) | |
| 7 | g.55201241C>G | CA454968544 | EGFR | c.2841C>G (p.Ala947=) c.900-4106C>G n.744C>G n.669C>G c.3000C>G (p.Ala1000=) c.*28+28313C>G (n.*28+28313C>G) c.2865C>G (p.Ala955=) c.2199C>G (p.Ala733=) | dbSNP |
| 7 | g.55201241C>T | CA454968545 | EGFR | c.2841C>T (p.Ala947=) c.900-4106C>T n.744C>T n.669C>T c.3000C>T (p.Ala1000=) c.*28+28313C>T (n.*28+28313C>T) c.2865C>T (p.Ala955=) c.2199C>T (p.Ala733=) | dbSNP |
| 7 | g.55201242C>A | CA367582447 | EGFR | c.2842C>A (p.Leu948Met) c.900-4105C>A n.745C>A n.670C>A c.3001C>A (p.Leu1001Met) c.*28+28314C>A (n.*28+28314C>A) c.2866C>A (p.Leu956Met) c.2200C>A (p.Leu734Met) | dbSNP |
| 7 | g.55201242C>G | CA367582448 | EGFR | c.2842C>G (p.Leu948Val) c.900-4105C>G n.745C>G n.670C>G c.3001C>G (p.Leu1001Val) c.*28+28314C>G (n.*28+28314C>G) c.2866C>G (p.Leu956Val) c.2200C>G (p.Leu734Val) | dbSNP |
| 7 | g.55201242C>T | CA454968547 | EGFR | c.2842C>T (p.Leu948=) c.900-4105C>T n.745C>T n.670C>T c.3001C>T (p.Leu1001=) c.*28+28314C>T (n.*28+28314C>T) c.2866C>T (p.Leu956=) c.2200C>T (p.Leu734=) | dbSNP |
| 7 | g.55201243T>A | CA367582451 | EGFR | c.2843T>A (p.Leu948Gln) c.900-4104T>A n.746T>A n.671T>A c.3002T>A (p.Leu1001Gln) c.*28+28315T>A (n.*28+28315T>A) c.2867T>A (p.Leu956Gln) c.2201T>A (p.Leu734Gln) | |
| 7 | g.55201243T>C | CA367582450 | EGFR | c.2843T>C (p.Leu948Pro) c.900-4104T>C n.746T>C n.671T>C c.3002T>C (p.Leu1001Pro) c.*28+28315T>C (n.*28+28315T>C) c.2867T>C (p.Leu956Pro) c.2201T>C (p.Leu734Pro) | |
| 7 | g.55201243T>G | CA367582449 | EGFR | c.2843T>G (p.Leu948Arg) c.900-4104T>G n.746T>G n.671T>G c.3002T>G (p.Leu1001Arg) c.*28+28315T>G (n.*28+28315T>G) c.2867T>G (p.Leu956Arg) c.2201T>G (p.Leu734Arg) | |
| 7 | g.55201244G>A | CA454968548 | EGFR | c.2844G>A (p.Leu948=) c.900-4103G>A n.747G>A n.672G>A c.3003G>A (p.Leu1001=) c.*28+28316G>A (n.*28+28316G>A) c.2868G>A (p.Leu956=) c.2202G>A (p.Leu734=) | ClinVar dbSNP |
| 7 | g.55201244G>C | CA454968550 | EGFR | c.2844G>C (p.Leu948=) c.900-4103G>C n.747G>C n.672G>C c.3003G>C (p.Leu1001=) c.*28+28316G>C (n.*28+28316G>C) c.2868G>C (p.Leu956=) c.2202G>C (p.Leu734=) | dbSNP |
| 7 | g.55201244G= | CA1708928430 | EGFR | c.2844G= (p.Leu948=) c.900-4103G= n.747G= n.672G= c.3003G= (p.Leu1001=) c.*28+28316G= (n.*28+28316G=) c.2868G= (p.Leu956=) c.2202G= (p.Leu734=) | |
| 7 | g.55201244G>T | CA454968549 | EGFR | c.2844G>T (p.Leu948=) c.900-4103G>T n.747G>T n.672G>T c.3003G>T (p.Leu1001=) c.*28+28316G>T (n.*28+28316G>T) c.2868G>T (p.Leu956=) c.2202G>T (p.Leu734=) | |
| 7 | g.55201245A= | CA1708928431 | EGFR | c.2845A= (p.Met949=) c.900-4102A= n.748A= n.673A= c.3004A= (p.Met1002=) c.*28+28317A= (n.*28+28317A=) c.2869A= (p.Met957=) c.2203A= (p.Met735=) | |
| 7 | g.55201245A>C | CA367582452 | EGFR | c.2845A>C (p.Met949Leu) c.900-4102A>C n.748A>C n.673A>C c.3004A>C (p.Met1002Leu) c.*28+28317A>C (n.*28+28317A>C) c.2869A>C (p.Met957Leu) c.2203A>C (p.Met735Leu) | |
| 7 | g.55201245A>G | CA367582453 | EGFR | c.2845A>G (p.Met949Val) c.900-4102A>G n.748A>G n.673A>G c.3004A>G (p.Met1002Val) c.*28+28317A>G (n.*28+28317A>G) c.2869A>G (p.Met957Val) c.2203A>G (p.Met735Val) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 7 | g.55201245A>T | CA367582454 | EGFR | c.2845A>T (p.Met949Leu) c.900-4102A>T n.748A>T n.673A>T c.3004A>T (p.Met1002Leu) c.*28+28317A>T (n.*28+28317A>T) c.2869A>T (p.Met957Leu) c.2203A>T (p.Met735Leu) | dbSNP |
| 7 | g.55201246T>A | CA367582455 | EGFR | c.2846T>A (p.Met949Lys) c.900-4101T>A n.749T>A n.674T>A c.3005T>A (p.Met1002Lys) c.*28+28318T>A (n.*28+28318T>A) c.2870T>A (p.Met957Lys) c.2204T>A (p.Met735Lys) | |
| 7 | g.55201246T>C | CA367582456 | EGFR | c.2846T>C (p.Met949Thr) c.900-4101T>C n.749T>C n.674T>C c.3005T>C (p.Met1002Thr) c.*28+28318T>C (n.*28+28318T>C) c.2870T>C (p.Met957Thr) c.2204T>C (p.Met735Thr) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 7 | g.55201246T>G | CA367582457 | EGFR | c.2846T>G (p.Met949Arg) c.900-4101T>G n.749T>G n.674T>G c.3005T>G (p.Met1002Arg) c.*28+28318T>G (n.*28+28318T>G) c.2870T>G (p.Met957Arg) c.2204T>G (p.Met735Arg) | |
| 7 | g.55201246T= | CA1708928432 | EGFR | c.2846T= (p.Met949=) c.900-4101T= n.749T= n.674T= c.3005T= (p.Met1002=) c.*28+28318T= (n.*28+28318T=) c.2870T= (p.Met957=) c.2204T= (p.Met735=) | |
| 7 | g.55201247G>A | CA367582458 | EGFR | c.2847G>A (p.Met949Ile) c.900-4100G>A n.750G>A n.675G>A c.3006G>A (p.Met1002Ile) c.*28+28319G>A (n.*28+28319G>A) c.2871G>A (p.Met957Ile) c.2205G>A (p.Met735Ile) | ClinVar dbSNP |
| 7 | g.55201247G>C | CA367582459 | EGFR | c.2847G>C (p.Met949Ile) c.900-4100G>C n.750G>C n.675G>C c.3006G>C (p.Met1002Ile) c.*28+28319G>C (n.*28+28319G>C) c.2871G>C (p.Met957Ile) c.2205G>C (p.Met735Ile) | dbSNP |
| 7 | g.55201247G>T | CA367582460 | EGFR | c.2847G>T (p.Met949Ile) c.900-4100G>T n.750G>T n.675G>T c.3006G>T (p.Met1002Ile) c.*28+28319G>T (n.*28+28319G>T) c.2871G>T (p.Met957Ile) c.2205G>T (p.Met735Ile) | dbSNP COSMIC |
| 7 | g.55201247_55201248insCTCCTC | CA2682856341 | EGFR | c.2847_2848insCTCCTC (p.Met949_Asp950insLeuLeu) c.900-4100_900-4099insCTCCTC n.750_751insCTCCTC n.675_676insCTCCTC c.3006_3007insCTCCTC (p.Met1002_Asp1003insLeuLeu) c.*28+28319_*28+28320insCTCCTC (n.*28+28319_*28+28320insCTCCTC) c.2871_2872insCTCCTC (p.Met957_Asp958insLeuLeu) c.2205_2206insCTCCTC (p.Met735_Asp736insLeuLeu) | gnomAD v4 |
| 7 | g.55201248G>A | CA367582461 | EGFR | c.2848G>A (p.Asp950Asn) c.900-4099G>A n.751G>A n.676G>A c.3007G>A (p.Asp1003Asn) c.*28+28320G>A (n.*28+28320G>A) c.2872G>A (p.Asp958Asn) c.2206G>A (p.Asp736Asn) | dbSNP gnomAD v2 gnomAD v4 |
| 7 | g.55201248G>C | CA367582462 | EGFR | c.2848G>C (p.Asp950His) c.900-4099G>C n.751G>C n.676G>C c.3007G>C (p.Asp1003His) c.*28+28320G>C (n.*28+28320G>C) c.2872G>C (p.Asp958His) c.2206G>C (p.Asp736His) | dbSNP |
| 7 | g.55201248G= | CA1708928433 | EGFR | c.2848G= (p.Asp950=) c.900-4099G= n.751G= n.676G= c.3007G= (p.Asp1003=) c.*28+28320G= (n.*28+28320G=) c.2872G= (p.Asp958=) c.2206G= (p.Asp736=) | |
| 7 | g.55201248G>T | CA367582463 | EGFR | c.2848G>T (p.Asp950Tyr) c.900-4099G>T n.751G>T n.676G>T c.3007G>T (p.Asp1003Tyr) c.*28+28320G>T (n.*28+28320G>T) c.2872G>T (p.Asp958Tyr) c.2206G>T (p.Asp736Tyr) | ClinVar dbSNP |
| 7 | g.55201249A>C | CA367582466 | EGFR | c.2849A>C (p.Asp950Ala) c.900-4098A>C n.752A>C n.677A>C c.3008A>C (p.Asp1003Ala) c.*28+28321A>C (n.*28+28321A>C) c.2873A>C (p.Asp958Ala) c.2207A>C (p.Asp736Ala) | |
| 7 | g.55201249A>G | CA367582465 | EGFR | c.2849A>G (p.Asp950Gly) c.900-4098A>G n.752A>G n.677A>G c.3008A>G (p.Asp1003Gly) c.*28+28321A>G (n.*28+28321A>G) c.2873A>G (p.Asp958Gly) c.2207A>G (p.Asp736Gly) | dbSNP |
| 7 | g.55201249A>T | CA367582464 | EGFR | c.2849A>T (p.Asp950Val) c.900-4098A>T n.752A>T n.677A>T c.3008A>T (p.Asp1003Val) c.*28+28321A>T (n.*28+28321A>T) c.2873A>T (p.Asp958Val) c.2207A>T (p.Asp736Val) | dbSNP |
| 7 | g.55201250T>A | CA367582467 | EGFR | c.2850T>A (p.Asp950Glu) c.900-4097T>A n.753T>A n.678T>A c.3009T>A (p.Asp1003Glu) c.*28+28322T>A (n.*28+28322T>A) c.2874T>A (p.Asp958Glu) c.2208T>A (p.Asp736Glu) | |
| 7 | g.55201250T>C | CA454968554 | EGFR | c.2850T>C (p.Asp950=) c.900-4097T>C n.753T>C n.678T>C c.3009T>C (p.Asp1003=) c.*28+28322T>C (n.*28+28322T>C) c.2874T>C (p.Asp958=) c.2208T>C (p.Asp736=) | gnomAD v4 |
| 7 | g.55201250T>G | CA367582468 | EGFR | c.2850T>G (p.Asp950Glu) c.900-4097T>G n.753T>G n.678T>G c.3009T>G (p.Asp1003Glu) c.*28+28322T>G (n.*28+28322T>G) c.2874T>G (p.Asp958Glu) c.2208T>G (p.Asp736Glu) | |
| 7 | g.55201250_55201253delinsTGAA | CA1708928434 | EGFR | c.2850_2853delinsTGAA (p.Asp950=) c.900-4097_900-4094delinsTGAA n.753_756delinsTGAA n.678_681delinsTGAA c.3009_3012delinsTGAA (p.Asp1003=) c.*28+28322_*28+28325delinsTGAA (n.*28+28322_*28+28325delinsTGAA) c.2874_2877delinsTGAA (p.Asp958=) c.2208_2211delinsTGAA (p.Asp736=) | |
| 7 | g.55201251G>A | CA367582469 | EGFR | c.2851G>A (p.Glu951Lys) c.900-4096G>A n.754G>A n.679G>A c.3010G>A (p.Glu1004Lys) c.*28+28323G>A (n.*28+28323G>A) c.2875G>A (p.Glu959Lys) c.2209G>A (p.Glu737Lys) | ClinVar dbSNP gnomAD v4 |
| 7 | g.55201251G>C | CA367582470 | EGFR | c.2851G>C (p.Glu951Gln) c.900-4096G>C n.754G>C n.679G>C c.3010G>C (p.Glu1004Gln) c.*28+28323G>C (n.*28+28323G>C) c.2875G>C (p.Glu959Gln) c.2209G>C (p.Glu737Gln) | dbSNP |
| 7 | g.55201251G>T | CA367582471 | EGFR | c.2851G>T (p.Glu951Ter) c.900-4096G>T n.754G>T n.679G>T c.3010G>T (p.Glu1004Ter) c.*28+28323G>T (n.*28+28323G>T) c.2875G>T (p.Glu959Ter) c.2209G>T (p.Glu737Ter) | |
| 7 | g.55201256_55201258dup | CA2739266427 | EGFR | c.2856_2858dup (p.Glu952_Asp953insGlu) c.900-4091_900-4089dup n.759_761dup n.684_686dup c.3015_3017dup (p.Glu1005_Asp1006insGlu) c.*28+28328_*28+28330dup (n.*28+28328_*28+28330dup) c.2880_2882dup (p.Glu960_Asp961insGlu) c.2214_2216dup (p.Glu738_Asp739insGlu) | ClinVar |
| 7 | g.55201256_55201258del | CA4266237 | EGFR | c.2856_2858del (p.Glu952del) c.900-4091_900-4089del n.759_761del n.684_686del c.3015_3017del (p.Glu1005del) c.*28+28328_*28+28330del (n.*28+28328_*28+28330del) c.2880_2882del (p.Glu960del) c.2214_2216del (p.Glu738del) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 7 | g.55201252A>C | CA367582474 | EGFR | c.2852A>C (p.Glu951Ala) c.900-4095A>C n.755A>C n.680A>C c.3011A>C (p.Glu1004Ala) c.*28+28324A>C (n.*28+28324A>C) c.2876A>C (p.Glu959Ala) c.2210A>C (p.Glu737Ala) | |
| 7 | g.55201252A>G | CA367582472 | EGFR | c.2852A>G (p.Glu951Gly) c.900-4095A>G n.755A>G n.680A>G c.3011A>G (p.Glu1004Gly) c.*28+28324A>G (n.*28+28324A>G) c.2876A>G (p.Glu959Gly) c.2210A>G (p.Glu737Gly) | dbSNP |
| 7 | g.55201252A>T | CA367582473 | EGFR | c.2852A>T (p.Glu951Val) c.900-4095A>T n.755A>T n.680A>T c.3011A>T (p.Glu1004Val) c.*28+28324A>T (n.*28+28324A>T) c.2876A>T (p.Glu959Val) c.2210A>T (p.Glu737Val) | dbSNP |
| 7 | g.55201253A>C | CA367582475 | EGFR | c.2853A>C (p.Glu951Asp) c.900-4094A>C n.756A>C n.681A>C c.3012A>C (p.Glu1004Asp) c.*28+28325A>C (n.*28+28325A>C) c.2877A>C (p.Glu959Asp) c.2211A>C (p.Glu737Asp) | |
| 7 | g.55201253A>G | CA454968558 | EGFR | c.2853A>G (p.Glu951=) c.900-4094A>G n.756A>G n.681A>G c.3012A>G (p.Glu1004=) c.*28+28325A>G (n.*28+28325A>G) c.2877A>G (p.Glu959=) c.2211A>G (p.Glu737=) | dbSNP |
| 7 | g.55201253A>T | CA367582476 | EGFR | c.2853A>T (p.Glu951Asp) c.900-4094A>T n.756A>T n.681A>T c.3012A>T (p.Glu1004Asp) c.*28+28325A>T (n.*28+28325A>T) c.2877A>T (p.Glu959Asp) c.2211A>T (p.Glu737Asp) | dbSNP |
| 7 | g.55201254G>A | CA367582477 | EGFR | c.2854G>A (p.Glu952Lys) c.900-4093G>A n.757G>A n.682G>A c.3013G>A (p.Glu1005Lys) c.*28+28326G>A (n.*28+28326G>A) c.2878G>A (p.Glu960Lys) c.2212G>A (p.Glu738Lys) | dbSNP gnomAD v4 |
| 7 | g.55201254G>C | CA367582478 | EGFR | c.2854G>C (p.Glu952Gln) c.900-4093G>C n.757G>C n.682G>C c.3013G>C (p.Glu1005Gln) c.*28+28326G>C (n.*28+28326G>C) c.2878G>C (p.Glu960Gln) c.2212G>C (p.Glu738Gln) | ClinVar dbSNP gnomAD v4 |
| 7 | g.55201254G>T | CA367582479 | EGFR | c.2854G>T (p.Glu952Ter) c.900-4093G>T n.757G>T n.682G>T c.3013G>T (p.Glu1005Ter) c.*28+28326G>T (n.*28+28326G>T) c.2878G>T (p.Glu960Ter) c.2212G>T (p.Glu738Ter) | dbSNP |
| 7 | g.55201255A= | CA1708928435 | EGFR | c.2855A= (p.Glu952=) c.900-4092A= n.758A= n.683A= c.3014A= (p.Glu1005=) c.*28+28327A= (n.*28+28327A=) c.2879A= (p.Glu960=) c.2213A= (p.Glu738=) | |
| 7 | g.55201255A>C | CA367582480 | EGFR | c.2855A>C (p.Glu952Ala) c.900-4092A>C n.758A>C n.683A>C c.3014A>C (p.Glu1005Ala) c.*28+28327A>C (n.*28+28327A>C) c.2879A>C (p.Glu960Ala) c.2213A>C (p.Glu738Ala) | |
| 7 | g.55201255A>G | CA367582482 | EGFR | c.2855A>G (p.Glu952Gly) c.900-4092A>G n.758A>G n.683A>G c.3014A>G (p.Glu1005Gly) c.*28+28327A>G (n.*28+28327A>G) c.2879A>G (p.Glu960Gly) c.2213A>G (p.Glu738Gly) | |
| 7 | g.55201255A>T | CA367582481 | EGFR | c.2855A>T (p.Glu952Val) c.900-4092A>T n.758A>T n.683A>T c.3014A>T (p.Glu1005Val) c.*28+28327A>T (n.*28+28327A>T) c.2879A>T (p.Glu960Val) c.2213A>T (p.Glu738Val) | ClinVar dbSNP |
| 7 | g.55201256A= | CA1708928436 | EGFR | c.2856A= (p.Glu952=) c.900-4091A= n.759A= n.684A= c.3015A= (p.Glu1005=) c.*28+28328A= (n.*28+28328A=) c.2880A= (p.Glu960=) c.2214A= (p.Glu738=) | |
| 7 | g.55201256A>C | CA367582483 | EGFR | c.2856A>C (p.Glu952Asp) c.900-4091A>C n.759A>C n.684A>C c.3015A>C (p.Glu1005Asp) c.*28+28328A>C (n.*28+28328A>C) c.2880A>C (p.Glu960Asp) c.2214A>C (p.Glu738Asp) | |
| 7 | g.55201256A>G | CA4266238 | EGFR | c.2856A>G (p.Glu952=) c.900-4091A>G n.759A>G n.684A>G c.3015A>G (p.Glu1005=) c.*28+28328A>G (n.*28+28328A>G) c.2880A>G (p.Glu960=) c.2214A>G (p.Glu738=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 7 | g.55201256A>T | CA367582484 | EGFR | c.2856A>T (p.Glu952Asp) c.900-4091A>T n.759A>T n.684A>T c.3015A>T (p.Glu1005Asp) c.*28+28328A>T (n.*28+28328A>T) c.2880A>T (p.Glu960Asp) c.2214A>T (p.Glu738Asp) | dbSNP |
| 7 | g.55201257G>A | CA367582485 | EGFR | c.2857G>A (p.Asp953Asn) c.900-4090G>A n.760G>A n.685G>A c.3016G>A (p.Asp1006Asn) c.*28+28329G>A (n.*28+28329G>A) c.2881G>A (p.Asp961Asn) c.2215G>A (p.Asp739Asn) | dbSNP |
| 7 | g.55201257G>C | CA367582486 | EGFR | c.2857G>C (p.Asp953His) c.900-4090G>C n.760G>C n.685G>C c.3016G>C (p.Asp1006His) c.*28+28329G>C (n.*28+28329G>C) c.2881G>C (p.Asp961His) c.2215G>C (p.Asp739His) | ClinVar dbSNP |
| 7 | g.55201257G= | CA1708928437 | EGFR | c.2857G= (p.Asp953=) c.900-4090G= n.760G= n.685G= c.3016G= (p.Asp1006=) c.*28+28329G= (n.*28+28329G=) c.2881G= (p.Asp961=) c.2215G= (p.Asp739=) | |
| 7 | g.55201257G>T | CA367582487 | EGFR | c.2857G>T (p.Asp953Tyr) c.900-4090G>T n.760G>T n.685G>T c.3016G>T (p.Asp1006Tyr) c.*28+28329G>T (n.*28+28329G>T) c.2881G>T (p.Asp961Tyr) c.2215G>T (p.Asp739Tyr) | |
| 7 | g.55201258A= | CA1708928438 | EGFR | c.2858A= (p.Asp953=) c.900-4089A= n.761A= n.686A= c.3017A= (p.Asp1006=) c.*28+28330A= (n.*28+28330A=) c.2882A= (p.Asp961=) c.2216A= (p.Asp739=) | |
| 7 | g.55201258A>C | CA4266239 | EGFR | c.2858A>C (p.Asp953Ala) c.900-4089A>C n.761A>C n.686A>C c.3017A>C (p.Asp1006Ala) c.*28+28330A>C (n.*28+28330A>C) c.2882A>C (p.Asp961Ala) c.2216A>C (p.Asp739Ala) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 7 | g.55201258A>G | CA367582488 | EGFR | c.2858A>G (p.Asp953Gly) c.900-4089A>G n.761A>G n.686A>G c.3017A>G (p.Asp1006Gly) c.*28+28330A>G (n.*28+28330A>G) c.2882A>G (p.Asp961Gly) c.2216A>G (p.Asp739Gly) | dbSNP gnomAD v4 |
| 7 | g.55201258A>T | CA367582489 | EGFR | c.2858A>T (p.Asp953Val) c.900-4089A>T n.761A>T n.686A>T c.3017A>T (p.Asp1006Val) c.*28+28330A>T (n.*28+28330A>T) c.2882A>T (p.Asp961Val) c.2216A>T (p.Asp739Val) | dbSNP gnomAD v4 |
| 7 | g.55201259C>A | CA367582490 | EGFR | c.2859C>A (p.Asp953Glu) c.900-4088C>A n.762C>A n.687C>A c.3018C>A (p.Asp1006Glu) c.*28+28331C>A (n.*28+28331C>A) c.2883C>A (p.Asp961Glu) c.2217C>A (p.Asp739Glu) | dbSNP |
| 7 | g.55201259C= | CA1708928439 | EGFR | c.2859C= (p.Asp953=) c.900-4088C= n.762C= n.687C= c.3018C= (p.Asp1006=) c.*28+28331C= (n.*28+28331C=) c.2883C= (p.Asp961=) c.2217C= (p.Asp739=) | |
| 7 | g.55201259C>G | CA367582491 | EGFR | c.2859C>G (p.Asp953Glu) c.900-4088C>G n.762C>G n.687C>G c.3018C>G (p.Asp1006Glu) c.*28+28331C>G (n.*28+28331C>G) c.2883C>G (p.Asp961Glu) c.2217C>G (p.Asp739Glu) | dbSNP |
| 7 | g.55201259C>T | CA454968561 | EGFR | c.2859C>T (p.Asp953=) c.900-4088C>T n.762C>T n.687C>T c.3018C>T (p.Asp1006=) c.*28+28331C>T (n.*28+28331C>T) c.2883C>T (p.Asp961=) c.2217C>T (p.Asp739=) | ClinVar dbSNP gnomAD v4 |
| 7 | g.55201260A= | CA1708928440 | EGFR | c.2860A= (p.Met954=) c.900-4087A= n.763A= n.688A= c.3019A= (p.Met1007=) c.*28+28332A= (n.*28+28332A=) c.2884A= (p.Met962=) c.2218A= (p.Met740=) | |
| 7 | g.55201260A>C | CA367582494 | EGFR | c.2860A>C (p.Met954Leu) c.900-4087A>C n.763A>C n.688A>C c.3019A>C (p.Met1007Leu) c.*28+28332A>C (n.*28+28332A>C) c.2884A>C (p.Met962Leu) c.2218A>C (p.Met740Leu) | |
| 7 | g.55201260A>G | CA367582493 | EGFR | c.2860A>G (p.Met954Val) c.900-4087A>G n.763A>G n.688A>G c.3019A>G (p.Met1007Val) c.*28+28332A>G (n.*28+28332A>G) c.2884A>G (p.Met962Val) c.2218A>G (p.Met740Val) | ClinVar dbSNP |
| 7 | g.55201260A>T | CA367582492 | EGFR | c.2860A>T (p.Met954Leu) c.900-4087A>T n.763A>T n.688A>T c.3019A>T (p.Met1007Leu) c.*28+28332A>T (n.*28+28332A>T) c.2884A>T (p.Met962Leu) c.2218A>T (p.Met740Leu) | ClinVar dbSNP |
| 7 | g.55201261T>A | CA367582495 | EGFR | c.2861T>A (p.Met954Lys) c.900-4086T>A n.764T>A n.689T>A c.3020T>A (p.Met1007Lys) c.*28+28333T>A (n.*28+28333T>A) c.2885T>A (p.Met962Lys) c.2219T>A (p.Met740Lys) | |
| 7 | g.55201261T>C | CA367582497 | EGFR | c.2861T>C (p.Met954Thr) c.900-4086T>C n.764T>C n.689T>C c.3020T>C (p.Met1007Thr) c.*28+28333T>C (n.*28+28333T>C) c.2885T>C (p.Met962Thr) c.2219T>C (p.Met740Thr) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 7 | g.55201261T>G | CA367582496 | EGFR | c.2861T>G (p.Met954Arg) c.900-4086T>G n.764T>G n.689T>G c.3020T>G (p.Met1007Arg) c.*28+28333T>G (n.*28+28333T>G) c.2885T>G (p.Met962Arg) c.2219T>G (p.Met740Arg) | |
| 7 | g.55201261T= | CA1708928441 | EGFR | c.2861T= (p.Met954=) c.900-4086T= n.764T= n.689T= c.3020T= (p.Met1007=) c.*28+28333T= (n.*28+28333T=) c.2885T= (p.Met962=) c.2219T= (p.Met740=) | |
| 7 | g.55201262G>A | CA367582498 | EGFR | c.2862G>A (p.Met954Ile) c.900-4085G>A n.765G>A n.690G>A c.3021G>A (p.Met1007Ile) c.*28+28334G>A (n.*28+28334G>A) c.2886G>A (p.Met962Ile) c.2220G>A (p.Met740Ile) | |
| 7 | g.55201262G>C | CA367582500 | EGFR | c.2862G>C (p.Met954Ile) c.900-4085G>C n.765G>C n.690G>C c.3021G>C (p.Met1007Ile) c.*28+28334G>C (n.*28+28334G>C) c.2886G>C (p.Met962Ile) c.2220G>C (p.Met740Ile) | |
| 7 | g.55201262G>T | CA367582499 | EGFR | c.2862G>T (p.Met954Ile) c.900-4085G>T n.765G>T n.690G>T c.3021G>T (p.Met1007Ile) c.*28+28334G>T (n.*28+28334G>T) c.2886G>T (p.Met962Ile) c.2220G>T (p.Met740Ile) | |
| 7 | g.55201263G>A | CA367582501 | EGFR | c.2863G>A (p.Asp955Asn) c.900-4084G>A n.766G>A n.691G>A c.3022G>A (p.Asp1008Asn) c.*28+28335G>A (n.*28+28335G>A) c.2887G>A (p.Asp963Asn) c.2221G>A (p.Asp741Asn) | ClinVar dbSNP |
| 7 | g.55201263G>C | CA367582503 | EGFR | c.2863G>C (p.Asp955His) c.900-4084G>C n.766G>C n.691G>C c.3022G>C (p.Asp1008His) c.*28+28335G>C (n.*28+28335G>C) c.2887G>C (p.Asp963His) c.2221G>C (p.Asp741His) | dbSNP |
| 7 | g.55201263G= | CA1708928442 | EGFR | c.2863G= (p.Asp955=) c.900-4084G= n.766G= n.691G= c.3022G= (p.Asp1008=) c.*28+28335G= (n.*28+28335G=) c.2887G= (p.Asp963=) c.2221G= (p.Asp741=) | |
| 7 | g.55201263G>T | CA367582502 | EGFR | c.2863G>T (p.Asp955Tyr) c.900-4084G>T n.766G>T n.691G>T c.3022G>T (p.Asp1008Tyr) c.*28+28335G>T (n.*28+28335G>T) c.2887G>T (p.Asp963Tyr) c.2221G>T (p.Asp741Tyr) | dbSNP |
| 7 | g.55201264A= | CA1708928443 | EGFR | c.2864A= (p.Asp955=) c.900-4083A= n.767A= n.692A= c.3023A= (p.Asp1008=) c.*28+28336A= (n.*28+28336A=) c.2888A= (p.Asp963=) c.2222A= (p.Asp741=) | |
| 7 | g.55201264A>C | CA367582504 | EGFR | c.2864A>C (p.Asp955Ala) c.900-4083A>C n.767A>C n.692A>C c.3023A>C (p.Asp1008Ala) c.*28+28336A>C (n.*28+28336A>C) c.2888A>C (p.Asp963Ala) c.2222A>C (p.Asp741Ala) | dbSNP |
| 7 | g.55201264A>G | CA367582506 | EGFR | c.2864A>G (p.Asp955Gly) c.900-4083A>G n.767A>G n.692A>G c.3023A>G (p.Asp1008Gly) c.*28+28336A>G (n.*28+28336A>G) c.2888A>G (p.Asp963Gly) c.2222A>G (p.Asp741Gly) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 7 | g.55201264A>T | CA367582505 | EGFR | c.2864A>T (p.Asp955Val) c.900-4083A>T n.767A>T n.692A>T c.3023A>T (p.Asp1008Val) c.*28+28336A>T (n.*28+28336A>T) c.2888A>T (p.Asp963Val) c.2222A>T (p.Asp741Val) | dbSNP |
| 7 | g.55201265C>A | CA4266240 | EGFR | c.2865C>A (p.Asp955Glu) c.900-4082C>A n.768C>A n.693C>A c.3024C>A (p.Asp1008Glu) c.*28+28337C>A (n.*28+28337C>A) c.2889C>A (p.Asp963Glu) c.2223C>A (p.Asp741Glu) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 7 | g.55201265C= | CA1708928444 | EGFR | c.2865C= (p.Asp955=) c.900-4082C= n.768C= n.693C= c.3024C= (p.Asp1008=) c.*28+28337C= (n.*28+28337C=) c.2889C= (p.Asp963=) c.2223C= (p.Asp741=) | |
| 7 | g.55201265C>G | CA367582507 | EGFR | c.2865C>G (p.Asp955Glu) c.900-4082C>G n.768C>G n.693C>G c.3024C>G (p.Asp1008Glu) c.*28+28337C>G (n.*28+28337C>G) c.2889C>G (p.Asp963Glu) c.2223C>G (p.Asp741Glu) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 7 | g.55201265C>T | CA158937860 | EGFR | c.2865C>T (p.Asp955=) c.900-4082C>T n.768C>T n.693C>T c.3024C>T (p.Asp1008=) c.*28+28337C>T (n.*28+28337C>T) c.2889C>T (p.Asp963=) c.2223C>T (p.Asp741=) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 7 | g.55201266G>A | CA4266241 | EGFR | c.2866G>A (p.Asp956Asn) c.900-4081G>A n.769G>A n.694G>A c.3025G>A (p.Asp1009Asn) c.*28+28338G>A (n.*28+28338G>A) c.2890G>A (p.Asp964Asn) c.2224G>A (p.Asp742Asn) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 7 | g.55201266G>C | CA367582508 | EGFR | c.2866G>C (p.Asp956His) c.900-4081G>C n.769G>C n.694G>C c.3025G>C (p.Asp1009His) c.*28+28338G>C (n.*28+28338G>C) c.2890G>C (p.Asp964His) c.2224G>C (p.Asp742His) | dbSNP |
| 7 | g.55201266G= | CA1708928445 | EGFR | c.2866G= (p.Asp956=) c.900-4081G= n.769G= n.694G= c.3025G= (p.Asp1009=) c.*28+28338G= (n.*28+28338G=) c.2890G= (p.Asp964=) c.2224G= (p.Asp742=) | |
| 7 | g.55201266G>T | CA367582509 | EGFR | c.2866G>T (p.Asp956Tyr) c.900-4081G>T n.769G>T n.694G>T c.3025G>T (p.Asp1009Tyr) c.*28+28338G>T (n.*28+28338G>T) c.2890G>T (p.Asp964Tyr) c.2224G>T (p.Asp742Tyr) | |
| 7 | g.55201267A>C | CA367582510 | EGFR | c.2867A>C (p.Asp956Ala) c.900-4080A>C n.770A>C n.695A>C c.3026A>C (p.Asp1009Ala) c.*28+28339A>C (n.*28+28339A>C) c.2891A>C (p.Asp964Ala) c.2225A>C (p.Asp742Ala) | dbSNP |
| 7 | g.55201267A>G | CA367582511 | EGFR | c.2867A>G (p.Asp956Gly) c.900-4080A>G n.770A>G n.695A>G c.3026A>G (p.Asp1009Gly) c.*28+28339A>G (n.*28+28339A>G) c.2891A>G (p.Asp964Gly) c.2225A>G (p.Asp742Gly) | dbSNP |
| 7 | g.55201267A>T | CA367582512 | EGFR | c.2867A>T (p.Asp956Val) c.900-4080A>T n.770A>T n.695A>T c.3026A>T (p.Asp1009Val) c.*28+28339A>T (n.*28+28339A>T) c.2891A>T (p.Asp964Val) c.2225A>T (p.Asp742Val) | dbSNP |
| 7 | g.55201268C>A | CA367582513 | EGFR | c.2868C>A (p.Asp956Glu) c.900-4079C>A n.771C>A n.696C>A c.3027C>A (p.Asp1009Glu) c.*28+28340C>A (n.*28+28340C>A) c.2892C>A (p.Asp964Glu) c.2226C>A (p.Asp742Glu) | |
| 7 | g.55201268C= | CA1708928446 | EGFR | c.2868C= (p.Asp956=) c.900-4079C= n.771C= n.696C= c.3027C= (p.Asp1009=) c.*28+28340C= (n.*28+28340C=) c.2892C= (p.Asp964=) c.2226C= (p.Asp742=) | |
| 7 | g.55201268C>G | CA367582514 | EGFR | c.2868C>G (p.Asp956Glu) c.900-4079C>G n.771C>G n.696C>G c.3027C>G (p.Asp1009Glu) c.*28+28340C>G (n.*28+28340C>G) c.2892C>G (p.Asp964Glu) c.2226C>G (p.Asp742Glu) | |
| 7 | g.55201268C>T | CA4266242 | EGFR | c.2868C>T (p.Asp956=) c.900-4079C>T n.771C>T n.696C>T c.3027C>T (p.Asp1009=) c.*28+28340C>T (n.*28+28340C>T) c.2892C>T (p.Asp964=) c.2226C>T (p.Asp742=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 7 | g.55201269G>A | CA4266243 | EGFR | c.2869G>A (p.Val957Met) c.900-4078G>A n.772G>A n.697G>A c.3028G>A (p.Val1010Met) c.*28+28341G>A (n.*28+28341G>A) c.2893G>A (p.Val965Met) c.2227G>A (p.Val743Met) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 7 | g.55201269G>C | CA367582516 | EGFR | c.2869G>C (p.Val957Leu) c.900-4078G>C n.772G>C n.697G>C c.3028G>C (p.Val1010Leu) c.*28+28341G>C (n.*28+28341G>C) c.2893G>C (p.Val965Leu) c.2227G>C (p.Val743Leu) | dbSNP gnomAD v2 gnomAD v4 |
| 7 | g.55201269G= | CA1708928447 | EGFR | c.2869G= (p.Val957=) c.900-4078G= n.772G= n.697G= c.3028G= (p.Val1010=) c.*28+28341G= (n.*28+28341G=) c.2893G= (p.Val965=) c.2227G= (p.Val743=) | |
| 7 | g.55201269G>T | CA367582515 | EGFR | c.2869G>T (p.Val957Leu) c.900-4078G>T n.772G>T n.697G>T c.3028G>T (p.Val1010Leu) c.*28+28341G>T (n.*28+28341G>T) c.2893G>T (p.Val965Leu) c.2227G>T (p.Val743Leu) | |
| 7 | g.55201270T>A | CA367582517 | EGFR | c.2870T>A (p.Val957Glu) c.900-4077T>A n.773T>A n.698T>A c.3029T>A (p.Val1010Glu) c.*28+28342T>A (n.*28+28342T>A) c.2894T>A (p.Val965Glu) c.2228T>A (p.Val743Glu) | |
| 7 | g.55201270T>C | CA367582518 | EGFR | c.2870T>C (p.Val957Ala) c.900-4077T>C n.773T>C n.698T>C c.3029T>C (p.Val1010Ala) c.*28+28342T>C (n.*28+28342T>C) c.2894T>C (p.Val965Ala) c.2228T>C (p.Val743Ala) | |
| 7 | g.55201270T>G | CA367582519 | EGFR | c.2870T>G (p.Val957Gly) c.900-4077T>G n.773T>G n.698T>G c.3029T>G (p.Val1010Gly) c.*28+28342T>G (n.*28+28342T>G) c.2894T>G (p.Val965Gly) c.2228T>G (p.Val743Gly) | |
| 7 | g.55201271G>A | CA454968571 | EGFR | c.2871G>A (p.Val957=) c.900-4076G>A n.774G>A n.699G>A c.3030G>A (p.Val1010=) c.*28+28343G>A (n.*28+28343G>A) c.2895G>A (p.Val965=) c.2229G>A (p.Val743=) | dbSNP gnomAD v4 |
| 7 | g.55201271G>C | CA454968568 | EGFR | c.2871G>C (p.Val957=) c.900-4076G>C n.774G>C n.699G>C c.3030G>C (p.Val1010=) c.*28+28343G>C (n.*28+28343G>C) c.2895G>C (p.Val965=) c.2229G>C (p.Val743=) | ClinVar dbSNP |
| 7 | g.55201271G>T | CA454968569 | EGFR | c.2871G>T (p.Val957=) c.900-4076G>T n.774G>T n.699G>T c.3030G>T (p.Val1010=) c.*28+28343G>T (n.*28+28343G>T) c.2895G>T (p.Val965=) c.2229G>T (p.Val743=) | dbSNP |
| 7 | g.55201272G>A | CA367582520 | EGFR | c.2872G>A (p.Val958Met) c.900-4075G>A n.775G>A n.700G>A c.3031G>A (p.Val1011Met) c.*28+28344G>A (n.*28+28344G>A) c.2896G>A (p.Val966Met) c.2230G>A (p.Val744Met) | dbSNP |
| 7 | g.55201272G>C | CA367582521 | EGFR | c.2872G>C (p.Val958Leu) c.900-4075G>C n.775G>C n.700G>C c.3031G>C (p.Val1011Leu) c.*28+28344G>C (n.*28+28344G>C) c.2896G>C (p.Val966Leu) c.2230G>C (p.Val744Leu) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 7 | g.55201272G= | CA1708928448 | EGFR | c.2872G= (p.Val958=) c.900-4075G= n.775G= n.700G= c.3031G= (p.Val1011=) c.*28+28344G= (n.*28+28344G=) c.2896G= (p.Val966=) c.2230G= (p.Val744=) | |
| 7 | g.55201272G>T | CA367582522 | EGFR | c.2872G>T (p.Val958Leu) c.900-4075G>T n.775G>T n.700G>T c.3031G>T (p.Val1011Leu) c.*28+28344G>T (n.*28+28344G>T) c.2896G>T (p.Val966Leu) c.2230G>T (p.Val744Leu) | dbSNP |
| 7 | g.55201273T>A | CA367582523 | EGFR | c.2873T>A (p.Val958Glu) c.900-4074T>A n.776T>A n.701T>A c.3032T>A (p.Val1011Glu) c.*28+28345T>A (n.*28+28345T>A) c.2897T>A (p.Val966Glu) c.2231T>A (p.Val744Glu) | |
| 7 | g.55201273T>C | CA367582524 | EGFR | c.2873T>C (p.Val958Ala) c.900-4074T>C n.776T>C n.701T>C c.3032T>C (p.Val1011Ala) c.*28+28345T>C (n.*28+28345T>C) c.2897T>C (p.Val966Ala) c.2231T>C (p.Val744Ala) | |
| 7 | g.55201273T>G | CA367582525 | EGFR | c.2873T>G (p.Val958Gly) c.900-4074T>G n.776T>G n.701T>G c.3032T>G (p.Val1011Gly) c.*28+28345T>G (n.*28+28345T>G) c.2897T>G (p.Val966Gly) c.2231T>G (p.Val744Gly) | dbSNP |
| 7 | g.55201274G>A | CA454968572 | EGFR | c.2874G>A (p.Val958=) c.900-4073G>A n.777G>A n.702G>A c.3033G>A (p.Val1011=) c.*28+28346G>A (n.*28+28346G>A) c.2898G>A (p.Val966=) c.2232G>A (p.Val744=) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 7 | g.55201274G>C | CA454968573 | EGFR | c.2874G>C (p.Val958=) c.900-4073G>C n.777G>C n.702G>C c.3033G>C (p.Val1011=) c.*28+28346G>C (n.*28+28346G>C) c.2898G>C (p.Val966=) c.2232G>C (p.Val744=) | |
| 7 | g.55201274G= | CA1708928449 | EGFR | c.2874G= (p.Val958=) c.900-4073G= n.777G= n.702G= c.3033G= (p.Val1011=) c.*28+28346G= (n.*28+28346G=) c.2898G= (p.Val966=) c.2232G= (p.Val744=) | |
| 7 | g.55201274G>T | CA454968574 | EGFR | c.2874G>T (p.Val958=) c.900-4073G>T n.777G>T n.702G>T c.3033G>T (p.Val1011=) c.*28+28346G>T (n.*28+28346G>T) c.2898G>T (p.Val966=) c.2232G>T (p.Val744=) | |
| 7 | g.55201275G>A | CA367582528 | EGFR | c.2875G>A (p.Asp959Asn) c.900-4072G>A n.778G>A n.703G>A c.3034G>A (p.Asp1012Asn) c.*28+28347G>A (n.*28+28347G>A) c.2899G>A (p.Asp967Asn) c.2233G>A (p.Asp745Asn) | dbSNP |
| 7 | g.55201275G>C | CA367582527 | EGFR | c.2875G>C (p.Asp959His) c.900-4072G>C n.778G>C n.703G>C c.3034G>C (p.Asp1012His) c.*28+28347G>C (n.*28+28347G>C) c.2899G>C (p.Asp967His) c.2233G>C (p.Asp745His) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 7 | g.55201275G= | CA1708928450 | EGFR | c.2875G= (p.Asp959=) c.900-4072G= n.778G= n.703G= c.3034G= (p.Asp1012=) c.*28+28347G= (n.*28+28347G=) c.2899G= (p.Asp967=) c.2233G= (p.Asp745=) | |
| 7 | g.55201275G>T | CA367582526 | EGFR | c.2875G>T (p.Asp959Tyr) c.900-4072G>T n.778G>T n.703G>T c.3034G>T (p.Asp1012Tyr) c.*28+28347G>T (n.*28+28347G>T) c.2899G>T (p.Asp967Tyr) c.2233G>T (p.Asp745Tyr) | dbSNP gnomAD v4 |
| 7 | g.55201276A>C | CA367582529 | EGFR | c.2876A>C (p.Asp959Ala) c.900-4071A>C n.779A>C n.704A>C c.3035A>C (p.Asp1012Ala) c.*28+28348A>C (n.*28+28348A>C) c.2900A>C (p.Asp967Ala) c.2234A>C (p.Asp745Ala) | dbSNP |
| 7 | g.55201276A>G | CA367582530 | EGFR | c.2876A>G (p.Asp959Gly) c.900-4071A>G n.779A>G n.704A>G c.3035A>G (p.Asp1012Gly) c.*28+28348A>G (n.*28+28348A>G) c.2900A>G (p.Asp967Gly) c.2234A>G (p.Asp745Gly) | dbSNP |
| 7 | g.55201276A>T | CA367582531 | EGFR | c.2876A>T (p.Asp959Val) c.900-4071A>T n.779A>T n.704A>T c.3035A>T (p.Asp1012Val) c.*28+28348A>T (n.*28+28348A>T) c.2900A>T (p.Asp967Val) c.2234A>T (p.Asp745Val) | dbSNP |
| 7 | g.55201277T>A | CA158937870 | EGFR | c.2877T>A (p.Asp959Glu) c.900-4070T>A n.780T>A n.705T>A c.3036T>A (p.Asp1012Glu) c.*28+28349T>A (n.*28+28349T>A) c.2901T>A (p.Asp967Glu) c.2235T>A (p.Asp745Glu) | dbSNP |
| 7 | g.55201277T>C | CA454968576 | EGFR | c.2877T>C (p.Asp959=) c.900-4070T>C n.780T>C n.705T>C c.3036T>C (p.Asp1012=) c.*28+28349T>C (n.*28+28349T>C) c.2901T>C (p.Asp967=) c.2235T>C (p.Asp745=) | ClinVar |
| 7 | g.55201277T>G | CA367582532 | EGFR | c.2877T>G (p.Asp959Glu) c.900-4070T>G n.780T>G n.705T>G c.3036T>G (p.Asp1012Glu) c.*28+28349T>G (n.*28+28349T>G) c.2901T>G (p.Asp967Glu) c.2235T>G (p.Asp745Glu) | dbSNP |
| 7 | g.55201277T= | CA1708928451 | EGFR | c.2877T= (p.Asp959=) c.900-4070T= n.780T= n.705T= c.3036T= (p.Asp1012=) c.*28+28349T= (n.*28+28349T=) c.2901T= (p.Asp967=) c.2235T= (p.Asp745=) | |
| 7 | g.55201278G>A | CA4266244 | EGFR | c.2878G>A (p.Ala960Thr) c.900-4069G>A n.781G>A n.706G>A c.3037G>A (p.Ala1013Thr) c.*28+28350G>A (n.*28+28350G>A) c.2902G>A (p.Ala968Thr) c.2236G>A (p.Ala746Thr) | dbSNP ExAC gnomAD v2 |
| 7 | g.55201278G>C | CA367582533 | EGFR | c.2878G>C (p.Ala960Pro) c.900-4069G>C n.781G>C n.706G>C c.3037G>C (p.Ala1013Pro) c.*28+28350G>C (n.*28+28350G>C) c.2902G>C (p.Ala968Pro) c.2236G>C (p.Ala746Pro) | dbSNP |
| 7 | g.55201278G= | CA1708928452 | EGFR | c.2878G= (p.Ala960=) c.900-4069G= n.781G= n.706G= c.3037G= (p.Ala1013=) c.*28+28350G= (n.*28+28350G=) c.2902G= (p.Ala968=) c.2236G= (p.Ala746=) | |
| 7 | g.55201278G>T | CA367582534 | EGFR | c.2878G>T (p.Ala960Ser) c.900-4069G>T n.781G>T n.706G>T c.3037G>T (p.Ala1013Ser) c.*28+28350G>T (n.*28+28350G>T) c.2902G>T (p.Ala968Ser) c.2236G>T (p.Ala746Ser) | |
| 7 | g.55201279C>A | CA367582535 | EGFR | c.2879C>A (p.Ala960Asp) c.900-4068C>A n.782C>A n.707C>A c.3038C>A (p.Ala1013Asp) c.*28+28351C>A (n.*28+28351C>A) c.2903C>A (p.Ala968Asp) c.2237C>A (p.Ala746Asp) | dbSNP |
| 7 | g.55201279C= | CA1708928453 | EGFR | c.2879C= (p.Ala960=) c.900-4068C= n.782C= n.707C= c.3038C= (p.Ala1013=) c.*28+28351C= (n.*28+28351C=) c.2903C= (p.Ala968=) c.2237C= (p.Ala746=) | |
| 7 | g.55201279C>G | CA367582536 | EGFR | c.2879C>G (p.Ala960Gly) c.900-4068C>G n.782C>G n.707C>G c.3038C>G (p.Ala1013Gly) c.*28+28351C>G (n.*28+28351C>G) c.2903C>G (p.Ala968Gly) c.2237C>G (p.Ala746Gly) | dbSNP |
| 7 | g.55201279C>T | CA158937877 | EGFR | c.2879C>T (p.Ala960Val) c.900-4068C>T n.782C>T n.707C>T c.3038C>T (p.Ala1013Val) c.*28+28351C>T (n.*28+28351C>T) c.2903C>T (p.Ala968Val) c.2237C>T (p.Ala746Val) | dbSNP gnomAD v4 |
| 7 | g.55201280C>A | CA454968577 | EGFR | c.2880C>A (p.Ala960=) c.900-4067C>A n.783C>A n.708C>A c.3039C>A (p.Ala1013=) c.*28+28352C>A (n.*28+28352C>A) c.2904C>A (p.Ala968=) c.2238C>A (p.Ala746=) | dbSNP |
| 7 | g.55201280C= | CA1708928454 | EGFR | c.2880C= (p.Ala960=) c.900-4067C= n.783C= n.708C= c.3039C= (p.Ala1013=) c.*28+28352C= (n.*28+28352C=) c.2904C= (p.Ala968=) c.2238C= (p.Ala746=) | |
| 7 | g.55201280C>G | CA454968578 | EGFR | c.2880C>G (p.Ala960=) c.900-4067C>G n.783C>G n.708C>G c.3039C>G (p.Ala1013=) c.*28+28352C>G (n.*28+28352C>G) c.2904C>G (p.Ala968=) c.2238C>G (p.Ala746=) | ClinVar dbSNP |
| 7 | g.55201280C>T | CA158937880 | EGFR | c.2880C>T (p.Ala960=) c.900-4067C>T n.783C>T n.708C>T c.3039C>T (p.Ala1013=) c.*28+28352C>T (n.*28+28352C>T) c.2904C>T (p.Ala968=) c.2238C>T (p.Ala746=) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 7 | g.55201281G>A | CA4266245 | EGFR | c.2881G>A (p.Asp961Asn) c.900-4066G>A n.784G>A n.709G>A c.3040G>A (p.Asp1014Asn) c.*28+28353G>A (n.*28+28353G>A) c.2905G>A (p.Asp969Asn) c.2239G>A (p.Asp747Asn) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 7 | g.55201281G>C | CA367582538 | EGFR | c.2881G>C (p.Asp961His) c.900-4066G>C n.784G>C n.709G>C c.3040G>C (p.Asp1014His) c.*28+28353G>C (n.*28+28353G>C) c.2905G>C (p.Asp969His) c.2239G>C (p.Asp747His) | dbSNP |
| 7 | g.55201281G= | CA1708928455 | EGFR | c.2881G= (p.Asp961=) c.900-4066G= n.784G= n.709G= c.3040G= (p.Asp1014=) c.*28+28353G= (n.*28+28353G=) c.2905G= (p.Asp969=) c.2239G= (p.Asp747=) | |
| 7 | g.55201281G>T | CA367582537 | EGFR | c.2881G>T (p.Asp961Tyr) c.900-4066G>T n.784G>T n.709G>T c.3040G>T (p.Asp1014Tyr) c.*28+28353G>T (n.*28+28353G>T) c.2905G>T (p.Asp969Tyr) c.2239G>T (p.Asp747Tyr) | dbSNP |
| 7 | g.55201282A>C | CA367582539 | EGFR | c.2882A>C (p.Asp961Ala) c.900-4065A>C n.785A>C n.710A>C c.3041A>C (p.Asp1014Ala) c.*28+28354A>C (n.*28+28354A>C) c.2906A>C (p.Asp969Ala) c.2240A>C (p.Asp747Ala) | dbSNP |
| 7 | g.55201282A>G | CA367582540 | EGFR | c.2882A>G (p.Asp961Gly) c.900-4065A>G n.785A>G n.710A>G c.3041A>G (p.Asp1014Gly) c.*28+28354A>G (n.*28+28354A>G) c.2906A>G (p.Asp969Gly) c.2240A>G (p.Asp747Gly) | dbSNP gnomAD v4 |
| 7 | g.55201282A>T | CA367582541 | EGFR | c.2882A>T (p.Asp961Val) c.900-4065A>T n.785A>T n.710A>T c.3041A>T (p.Asp1014Val) c.*28+28354A>T (n.*28+28354A>T) c.2906A>T (p.Asp969Val) c.2240A>T (p.Asp747Val) | dbSNP |
| 7 | g.55201283C>A | CA367582542 | EGFR | c.2883C>A (p.Asp961Glu) c.900-4064C>A n.786C>A n.711C>A c.3042C>A (p.Asp1014Glu) c.*28+28355C>A (n.*28+28355C>A) c.2907C>A (p.Asp969Glu) c.2241C>A (p.Asp747Glu) | dbSNP |
| 7 | g.55201283C= | CA1708928456 | EGFR | c.2883C= (p.Asp961=) c.900-4064C= n.786C= n.711C= c.3042C= (p.Asp1014=) c.*28+28355C= (n.*28+28355C=) c.2907C= (p.Asp969=) c.2241C= (p.Asp747=) | |
| 7 | g.55201283C>G | CA367582543 | EGFR | c.2883C>G (p.Asp961Glu) c.900-4064C>G n.786C>G n.711C>G c.3042C>G (p.Asp1014Glu) c.*28+28355C>G (n.*28+28355C>G) c.2907C>G (p.Asp969Glu) c.2241C>G (p.Asp747Glu) | dbSNP |
| 7 | g.55201283C>T | CA4266246 | EGFR | c.2883C>T (p.Asp961=) c.900-4064C>T n.786C>T n.711C>T c.3042C>T (p.Asp1014=) c.*28+28355C>T (n.*28+28355C>T) c.2907C>T (p.Asp969=) c.2241C>T (p.Asp747=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 7 | g.55201284G>A | CA367582544 | EGFR | c.2884G>A (p.Glu962Lys) c.900-4063G>A n.787G>A n.712G>A c.3043G>A (p.Glu1015Lys) c.*28+28356G>A (n.*28+28356G>A) c.2908G>A (p.Glu970Lys) c.2242G>A (p.Glu748Lys) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 7 | g.55201284G>C | CA367582545 | EGFR | c.2884G>C (p.Glu962Gln) c.900-4063G>C n.787G>C n.712G>C c.3043G>C (p.Glu1015Gln) c.*28+28356G>C (n.*28+28356G>C) c.2908G>C (p.Glu970Gln) c.2242G>C (p.Glu748Gln) | dbSNP |
| 7 | g.55201284G= | CA1708928457 | EGFR | c.2884G= (p.Glu962=) c.900-4063G= n.787G= n.712G= c.3043G= (p.Glu1015=) c.*28+28356G= (n.*28+28356G=) c.2908G= (p.Glu970=) c.2242G= (p.Glu748=) | |
| 7 | g.55201284G>T | CA367582546 | EGFR | c.2884G>T (p.Glu962Ter) c.900-4063G>T n.787G>T n.712G>T c.3043G>T (p.Glu1015Ter) c.*28+28356G>T (n.*28+28356G>T) c.2908G>T (p.Glu970Ter) c.2242G>T (p.Glu748Ter) | dbSNP |
| 7 | g.55201285A>C | CA367582547 | EGFR | c.2885A>C (p.Glu962Ala) c.900-4062A>C n.788A>C n.713A>C c.3044A>C (p.Glu1015Ala) c.*28+28357A>C (n.*28+28357A>C) c.2909A>C (p.Glu970Ala) c.2243A>C (p.Glu748Ala) | |
| 7 | g.55201285A>G | CA367582548 | EGFR | c.2885A>G (p.Glu962Gly) c.900-4062A>G n.788A>G n.713A>G c.3044A>G (p.Glu1015Gly) c.*28+28357A>G (n.*28+28357A>G) c.2909A>G (p.Glu970Gly) c.2243A>G (p.Glu748Gly) | |
| 7 | g.55201285A>T | CA367582549 | EGFR | c.2885A>T (p.Glu962Val) c.900-4062A>T n.788A>T n.713A>T c.3044A>T (p.Glu1015Val) c.*28+28357A>T (n.*28+28357A>T) c.2909A>T (p.Glu970Val) c.2243A>T (p.Glu748Val) | dbSNP |
| 7 | g.55201286G>A | CA454968579 | EGFR | c.2886G>A (p.Glu962=) c.900-4061G>A n.789G>A n.714G>A c.3045G>A (p.Glu1015=) c.*28+28358G>A (n.*28+28358G>A) c.2910G>A (p.Glu970=) c.2244G>A (p.Glu748=) | ClinVar dbSNP gnomAD v4 |
| 7 | g.55201286G>C | CA367582551 | EGFR | c.2886G>C (p.Glu962Asp) c.900-4061G>C n.789G>C n.714G>C c.3045G>C (p.Glu1015Asp) c.*28+28358G>C (n.*28+28358G>C) c.2910G>C (p.Glu970Asp) c.2244G>C (p.Glu748Asp) | dbSNP |
| 7 | g.55201286G>T | CA367582550 | EGFR | c.2886G>T (p.Glu962Asp) c.900-4061G>T n.789G>T n.714G>T c.3045G>T (p.Glu1015Asp) c.*28+28358G>T (n.*28+28358G>T) c.2910G>T (p.Glu970Asp) c.2244G>T (p.Glu748Asp) | |
| 7 | g.55201287del | CA2682856426 | EGFR | c.2887del (p.Tyr963ThrfsTer20) c.900-4060del n.790del n.715del c.3046del (p.Tyr1016ThrfsTer20) c.*28+28359del (n.*28+28359del) c.2911del (p.Tyr971ThrfsTer20) c.2245del (p.Tyr749ThrfsTer20) | gnomAD v4 |
| 7 | g.55201287T>A | CA367582552 | EGFR | c.2887T>A (p.Tyr963Asn) c.900-4060T>A n.790T>A n.715T>A c.3046T>A (p.Tyr1016Asn) c.*28+28359T>A (n.*28+28359T>A) c.2911T>A (p.Tyr971Asn) c.2245T>A (p.Tyr749Asn) | dbSNP |
| 7 | g.55201287T>C | CA367582554 | EGFR | c.2887T>C (p.Tyr963His) c.900-4060T>C n.790T>C n.715T>C c.3046T>C (p.Tyr1016His) c.*28+28359T>C (n.*28+28359T>C) c.2911T>C (p.Tyr971His) c.2245T>C (p.Tyr749His) | dbSNP |
| 7 | g.55201287T>G | CA367582553 | EGFR | c.2887T>G (p.Tyr963Asp) c.900-4060T>G n.790T>G n.715T>G c.3046T>G (p.Tyr1016Asp) c.*28+28359T>G (n.*28+28359T>G) c.2911T>G (p.Tyr971Asp) c.2245T>G (p.Tyr749Asp) | dbSNP |
| 7 | g.55201287_55201288insG | CA2775504558 | EGFR | c.2887_2888insG (p.Tyr963Ter) c.900-4060_900-4059insG n.790_791insG n.715_716insG c.3046_3047insG (p.Tyr1016Ter) c.*28+28359_*28+28360insG (n.*28+28359_*28+28360insG) c.2911_2912insG (p.Tyr971Ter) c.2245_2246insG (p.Tyr749Ter) | |
| 7 | g.55201287_55201288insTGAATTGTGTAG | CA2682856430 | EGFR | c.2887_2888insTGAATTGTGTAG (p.Tyr963delinsLeuAsnCysValAsp) c.900-4060_900-4059insTGAATTGTGTAG n.790_791insTGAATTGTGTAG n.715_716insTGAATTGTGTAG c.3046_3047insTGAATTGTGTAG (p.Tyr1016delinsLeuAsnCysValAsp) c.*28+28359_*28+28360insTGAATTGTGTAG (n.*28+28359_*28+28360insTGAATTGTGTAG) c.2911_2912insTGAATTGTGTAG (p.Tyr971delinsLeuAsnCysValAsp) c.2245_2246insTGAATTGTGTAG (p.Tyr749delinsLeuAsnCysValAsp) | gnomAD v4 |
| 7 | g.55201288A>C | CA367582555 | EGFR | c.2888A>C (p.Tyr963Ser) c.900-4059A>C n.791A>C n.716A>C c.3047A>C (p.Tyr1016Ser) c.*28+28360A>C (n.*28+28360A>C) c.2912A>C (p.Tyr971Ser) c.2246A>C (p.Tyr749Ser) | dbSNP |
| 7 | g.55201288A>G | CA367582556 | EGFR | c.2888A>G (p.Tyr963Cys) c.900-4059A>G n.791A>G n.716A>G c.3047A>G (p.Tyr1016Cys) c.*28+28360A>G (n.*28+28360A>G) c.2912A>G (p.Tyr971Cys) c.2246A>G (p.Tyr749Cys) | ClinVar |
| 7 | g.55201288A>T | CA367582557 | EGFR | c.2888A>T (p.Tyr963Phe) c.900-4059A>T n.791A>T n.716A>T c.3047A>T (p.Tyr1016Phe) c.*28+28360A>T (n.*28+28360A>T) c.2912A>T (p.Tyr971Phe) c.2246A>T (p.Tyr749Phe) | |
| 7 | g.55201288_55201290del | CA2682856432 | EGFR | c.2888_2890del (p.Tyr963_Leu964delinsPhe) c.900-4059_900-4057del n.791_793del n.716_718del c.3047_3049del (p.Tyr1016_Leu1017delinsPhe) c.*28+28360_*28+28362del (n.*28+28360_*28+28362del) c.2912_2914del (p.Tyr971_Leu972delinsPhe) c.2246_2248del (p.Tyr749_Leu750delinsPhe) | gnomAD v4 |
| 7 | g.55201288_55201298del | CA2682856433 | EGFR | c.2888_2898del (p.Tyr963SerfsTer?) c.900-4059_900-4049del n.791_801del n.716_726del c.3047_3057del (p.Tyr1016SerfsTer?) c.*28+28360_*28+28370del (n.*28+28360_*28+28370del) c.2912_2922del (p.Tyr971SerfsTer?) c.2246_2256del (p.Tyr749SerfsTer?) | gnomAD v4 |
| 7 | g.55201289C>A | CA367582558 | EGFR | c.2889C>A (p.Tyr963Ter) c.900-4058C>A n.792C>A n.717C>A c.3048C>A (p.Tyr1016Ter) c.*28+28361C>A (n.*28+28361C>A) c.2913C>A (p.Tyr971Ter) c.2247C>A (p.Tyr749Ter) | dbSNP |
| 7 | g.55201289C>G | CA367582559 | EGFR | c.2889C>G (p.Tyr963Ter) c.900-4058C>G n.792C>G n.717C>G c.3048C>G (p.Tyr1016Ter) c.*28+28361C>G (n.*28+28361C>G) c.2913C>G (p.Tyr971Ter) c.2247C>G (p.Tyr749Ter) | dbSNP |
| 7 | g.55201289C>T | CA454968580 | EGFR | c.2889C>T (p.Tyr963=) c.900-4058C>T n.792C>T n.717C>T c.3048C>T (p.Tyr1016=) c.*28+28361C>T (n.*28+28361C>T) c.2913C>T (p.Tyr971=) c.2247C>T (p.Tyr749=) | dbSNP gnomAD v4 |
| 7 | g.55201289_55201292del | CA2682856435 | EGFR | c.2889_2892del (p.Tyr963Ter) c.900-4058_900-4055del n.792_795del n.717_720del c.3048_3051del (p.Tyr1016Ter) c.*28+28361_*28+28364del (n.*28+28361_*28+28364del) c.2913_2916del (p.Tyr971Ter) c.2247_2250del (p.Tyr749Ter) | gnomAD v4 |
| 7 | g.55201289_55201299del | CA2775504562 | EGFR | c.2889_2899del (p.Tyr963Ter) c.900-4058_900-4048del n.792_802del n.717_727del c.3048_3058del (p.Tyr1016Ter) c.*28+28361_*28+28371del (n.*28+28361_*28+28371del) c.2913_2923del (p.Tyr971Ter) c.2247_2257del (p.Tyr749Ter) | |
| 7 | g.55201290C>A | CA367582560 | EGFR | c.2890C>A (p.Leu964Ile) c.900-4057C>A n.793C>A n.718C>A c.3049C>A (p.Leu1017Ile) c.*28+28362C>A (n.*28+28362C>A) c.2914C>A (p.Leu972Ile) c.2248C>A (p.Leu750Ile) | |
| 7 | g.55201290C= | CA1708928458 | EGFR | c.2890C= (p.Leu964=) c.900-4057C= n.793C= n.718C= c.3049C= (p.Leu1017=) c.*28+28362C= (n.*28+28362C=) c.2914C= (p.Leu972=) c.2248C= (p.Leu750=) | |
| 7 | g.55201290C>G | CA367582561 | EGFR | c.2890C>G (p.Leu964Val) c.900-4057C>G n.793C>G n.718C>G c.3049C>G (p.Leu1017Val) c.*28+28362C>G (n.*28+28362C>G) c.2914C>G (p.Leu972Val) c.2248C>G (p.Leu750Val) | |
| 7 | g.55201290C>T | CA367582562 | EGFR | c.2890C>T (p.Leu964Phe) c.900-4057C>T n.793C>T n.718C>T c.3049C>T (p.Leu1017Phe) c.*28+28362C>T (n.*28+28362C>T) c.2914C>T (p.Leu972Phe) c.2248C>T (p.Leu750Phe) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 7 | g.55201291T>A | CA367582563 | EGFR | c.2891T>A (p.Leu964His) c.900-4056T>A n.794T>A n.719T>A c.3050T>A (p.Leu1017His) c.*28+28363T>A (n.*28+28363T>A) c.2915T>A (p.Leu972His) c.2249T>A (p.Leu750His) | dbSNP |
| 7 | g.55201291T>C | CA367582564 | EGFR | c.2891T>C (p.Leu964Pro) c.900-4056T>C n.794T>C n.719T>C c.3050T>C (p.Leu1017Pro) c.*28+28363T>C (n.*28+28363T>C) c.2915T>C (p.Leu972Pro) c.2249T>C (p.Leu750Pro) | dbSNP |
| 7 | g.55201291T>G | CA367582565 | EGFR | c.2891T>G (p.Leu964Arg) c.900-4056T>G n.794T>G n.719T>G c.3050T>G (p.Leu1017Arg) c.*28+28363T>G (n.*28+28363T>G) c.2915T>G (p.Leu972Arg) c.2249T>G (p.Leu750Arg) | |
| 7 | g.55201292C>A | CA454968581 | EGFR | c.2892C>A (p.Leu964=) c.900-4055C>A n.795C>A n.720C>A c.3051C>A (p.Leu1017=) c.*28+28364C>A (n.*28+28364C>A) c.2916C>A (p.Leu972=) c.2250C>A (p.Leu750=) | ClinVar dbSNP gnomAD v4 |
| 7 | g.55201292C= | CA1708928459 | EGFR | c.2892C= (p.Leu964=) c.900-4055C= n.795C= n.720C= c.3051C= (p.Leu1017=) c.*28+28364C= (n.*28+28364C=) c.2916C= (p.Leu972=) c.2250C= (p.Leu750=) | |
| 7 | g.55201292C>G | CA454968582 | EGFR | c.2892C>G (p.Leu964=) c.900-4055C>G n.795C>G n.720C>G c.3051C>G (p.Leu1017=) c.*28+28364C>G (n.*28+28364C>G) c.2916C>G (p.Leu972=) c.2250C>G (p.Leu750=) | dbSNP |
| 7 | g.55201292C>T | CA4266247 | EGFR | c.2892C>T (p.Leu964=) c.900-4055C>T n.795C>T n.720C>T c.3051C>T (p.Leu1017=) c.*28+28364C>T (n.*28+28364C>T) c.2916C>T (p.Leu972=) c.2250C>T (p.Leu750=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 7 | g.55201292_55201299del | CA2682856444 | EGFR | c.2892_2899del (p.Ile965AlafsTer?) c.900-4055_900-4048del n.795_802del n.720_727del c.3051_3058del (p.Ile1018AlafsTer?) c.*28+28364_*28+28371del (n.*28+28364_*28+28371del) c.2916_2923del (p.Ile973AlafsTer?) c.2250_2257del (p.Ile751AlafsTer?) | gnomAD v4 |
| 7 | g.55201293A= | CA1708928460 | EGFR | c.2893A= (p.Ile965=) c.900-4054A= n.796A= n.721A= c.3052A= (p.Ile1018=) c.*28+28365A= (n.*28+28365A=) c.2917A= (p.Ile973=) c.2251A= (p.Ile751=) | |
| 7 | g.55201293A>C | CA367582566 | EGFR | c.2893A>C (p.Ile965Leu) c.900-4054A>C n.796A>C n.721A>C c.3052A>C (p.Ile1018Leu) c.*28+28365A>C (n.*28+28365A>C) c.2917A>C (p.Ile973Leu) c.2251A>C (p.Ile751Leu) | ClinVar dbSNP gnomAD v4 |
| 7 | g.55201293A>G | CA367582568 | EGFR | c.2893A>G (p.Ile965Val) c.900-4054A>G n.796A>G n.721A>G c.3052A>G (p.Ile1018Val) c.*28+28365A>G (n.*28+28365A>G) c.2917A>G (p.Ile973Val) c.2251A>G (p.Ile751Val) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 7 | g.55201293A>T | CA367582567 | EGFR | c.2893A>T (p.Ile965Phe) c.900-4054A>T n.796A>T n.721A>T c.3052A>T (p.Ile1018Phe) c.*28+28365A>T (n.*28+28365A>T) c.2917A>T (p.Ile973Phe) c.2251A>T (p.Ile751Phe) | dbSNP |
| 7 | g.55201293_55201303del | CA2682856449 | EGFR | c.2893_2903del (p.Ile965GlyfsTer30) c.900-4054_900-4044del n.796_806del n.721_731del c.3052_3062del (p.Ile1018GlyfsTer30) c.*28+28365_*28+28375del (n.*28+28365_*28+28375del) c.2917_2927del (p.Ile973GlyfsTer30) c.2251_2261del (p.Ile751GlyfsTer30) | gnomAD v4 |
| 7 | g.55201294T>A | CA367582569 | EGFR | c.2894T>A (p.Ile965Asn) c.900-4053T>A n.797T>A n.722T>A c.3053T>A (p.Ile1018Asn) c.*28+28366T>A (n.*28+28366T>A) c.2918T>A (p.Ile973Asn) c.2252T>A (p.Ile751Asn) | |
| 7 | g.55201294T>C | CA367582570 | EGFR | c.2894T>C (p.Ile965Thr) c.900-4053T>C n.797T>C n.722T>C c.3053T>C (p.Ile1018Thr) c.*28+28366T>C (n.*28+28366T>C) c.2918T>C (p.Ile973Thr) c.2252T>C (p.Ile751Thr) | |
| 7 | g.55201294T>G | CA367582571 | EGFR | c.2894T>G (p.Ile965Ser) c.900-4053T>G n.797T>G n.722T>G c.3053T>G (p.Ile1018Ser) c.*28+28366T>G (n.*28+28366T>G) c.2918T>G (p.Ile973Ser) c.2252T>G (p.Ile751Ser) | |
| 7 | g.55201295C>A | CA454968588 | EGFR | c.2895C>A (p.Ile965=) c.900-4052C>A n.798C>A n.723C>A c.3054C>A (p.Ile1018=) c.*28+28367C>A (n.*28+28367C>A) c.2919C>A (p.Ile973=) c.2253C>A (p.Ile751=) | ClinVar dbSNP |
| 7 | g.55201295C>G | CA367582572 | EGFR | c.2895C>G (p.Ile965Met) c.900-4052C>G n.798C>G n.723C>G c.3054C>G (p.Ile1018Met) c.*28+28367C>G (n.*28+28367C>G) c.2919C>G (p.Ile973Met) c.2253C>G (p.Ile751Met) | dbSNP |
| 7 | g.55201295C>T | CA454968590 | EGFR | c.2895C>T (p.Ile965=) c.900-4052C>T n.798C>T n.723C>T c.3054C>T (p.Ile1018=) c.*28+28367C>T (n.*28+28367C>T) c.2919C>T (p.Ile973=) c.2253C>T (p.Ile751=) | dbSNP gnomAD v4 |
| 7 | g.55201295_55201297del | CA2682856451 | EGFR | c.2895_2897del (p.Pro966del) c.900-4052_900-4050del n.798_800del n.723_725del c.3054_3056del (p.Pro1019del) c.*28+28367_*28+28369del (n.*28+28367_*28+28369del) c.2919_2921del (p.Pro974del) c.2253_2255del (p.Pro752del) | gnomAD v4 |
| 7 | g.55201296C>A | CA367582573 | EGFR | c.2896C>A (p.Pro966Thr) c.900-4051C>A n.799C>A n.724C>A c.3055C>A (p.Pro1019Thr) c.*28+28368C>A (n.*28+28368C>A) c.2920C>A (p.Pro974Thr) c.2254C>A (p.Pro752Thr) | ClinVar dbSNP |
| 7 | g.55201296C= | CA1708928461 | EGFR | c.2896C= (p.Pro966=) c.900-4051C= n.799C= n.724C= c.3055C= (p.Pro1019=) c.*28+28368C= (n.*28+28368C=) c.2920C= (p.Pro974=) c.2254C= (p.Pro752=) | |
| 7 | g.55201296C>G | CA367582574 | EGFR | c.2896C>G (p.Pro966Ala) c.900-4051C>G n.799C>G n.724C>G c.3055C>G (p.Pro1019Ala) c.*28+28368C>G (n.*28+28368C>G) c.2920C>G (p.Pro974Ala) c.2254C>G (p.Pro752Ala) | dbSNP gnomAD v4 |
| 7 | g.55201296C>T | CA367582575 | EGFR | c.2896C>T (p.Pro966Ser) c.900-4051C>T n.799C>T n.724C>T c.3055C>T (p.Pro1019Ser) c.*28+28368C>T (n.*28+28368C>T) c.2920C>T (p.Pro974Ser) c.2254C>T (p.Pro752Ser) | ClinVar dbSNP |
| 7 | g.55201297C>A | CA367582576 | EGFR | c.2897C>A (p.Pro966Gln) c.900-4050C>A n.800C>A n.725C>A c.3056C>A (p.Pro1019Gln) c.*28+28369C>A (n.*28+28369C>A) c.2921C>A (p.Pro974Gln) c.2255C>A (p.Pro752Gln) | ClinVar dbSNP |
| 7 | g.55201297C= | CA1708928462 | EGFR | c.2897C= (p.Pro966=) c.900-4050C= n.800C= n.725C= c.3056C= (p.Pro1019=) c.*28+28369C= (n.*28+28369C=) c.2921C= (p.Pro974=) c.2255C= (p.Pro752=) | |
| 7 | g.55201297C>G | CA367582577 | EGFR | c.2897C>G (p.Pro966Arg) c.900-4050C>G n.800C>G n.725C>G c.3056C>G (p.Pro1019Arg) c.*28+28369C>G (n.*28+28369C>G) c.2921C>G (p.Pro974Arg) c.2255C>G (p.Pro752Arg) | dbSNP |
| 7 | g.55201297C>T | CA367582578 | EGFR | c.2897C>T (p.Pro966Leu) c.900-4050C>T n.800C>T n.725C>T c.3056C>T (p.Pro1019Leu) c.*28+28369C>T (n.*28+28369C>T) c.2921C>T (p.Pro974Leu) c.2255C>T (p.Pro752Leu) | ClinVar dbSNP COSMIC |
| 7 | g.55201297_55201303del | CA2682856454 | EGFR | c.2897_2903del (p.Pro966ArgfsTer15) c.900-4050_900-4044del n.800_806del n.725_731del c.3056_3062del (p.Pro1019ArgfsTer15) c.*28+28369_*28+28375del (n.*28+28369_*28+28375del) c.2921_2927del (p.Pro974ArgfsTer15) c.2255_2261del (p.Pro752ArgfsTer15) | gnomAD v4 |
| 7 | g.55201298A>C | CA454968595 | EGFR | c.2898A>C (p.Pro966=) c.900-4049A>C n.801A>C n.726A>C c.3057A>C (p.Pro1019=) c.*28+28370A>C (n.*28+28370A>C) c.2922A>C (p.Pro974=) c.2256A>C (p.Pro752=) | ClinVar dbSNP gnomAD v4 |
| 7 | g.55201298A>G | CA454968596 | EGFR | c.2898A>G (p.Pro966=) c.900-4049A>G n.801A>G n.726A>G c.3057A>G (p.Pro1019=) c.*28+28370A>G (n.*28+28370A>G) c.2922A>G (p.Pro974=) c.2256A>G (p.Pro752=) | |
| 7 | g.55201298A>T | CA454968597 | EGFR | c.2898A>T (p.Pro966=) c.900-4049A>T n.801A>T n.726A>T c.3057A>T (p.Pro1019=) c.*28+28370A>T (n.*28+28370A>T) c.2922A>T (p.Pro974=) c.2256A>T (p.Pro752=) | dbSNP |
| 7 | g.55201299C>A | CA367582580 | EGFR | c.2899C>A (p.Gln967Lys) c.900-4048C>A n.802C>A n.727C>A c.3058C>A (p.Gln1020Lys) c.*28+28371C>A (n.*28+28371C>A) c.2923C>A (p.Gln975Lys) c.2257C>A (p.Gln753Lys) | |
| 7 | g.55201299C= | CA1708928463 | EGFR | c.2899C= (p.Gln967=) c.900-4048C= n.802C= n.727C= c.3058C= (p.Gln1020=) c.*28+28371C= (n.*28+28371C=) c.2923C= (p.Gln975=) c.2257C= (p.Gln753=) | |
| 7 | g.55201299C>G | CA367582581 | EGFR | c.2899C>G (p.Gln967Glu) c.900-4048C>G n.802C>G n.727C>G c.3058C>G (p.Gln1020Glu) c.*28+28371C>G (n.*28+28371C>G) c.2923C>G (p.Gln975Glu) c.2257C>G (p.Gln753Glu) | ClinVar dbSNP gnomAD v4 |
| 7 | g.55201299C>T | CA367582579 | EGFR | c.2899C>T (p.Gln967Ter) c.900-4048C>T n.802C>T n.727C>T c.3058C>T (p.Gln1020Ter) c.*28+28371C>T (n.*28+28371C>T) c.2923C>T (p.Gln975Ter) c.2257C>T (p.Gln753Ter) | |
| 7 | g.55201300A>C | CA367582582 | EGFR | c.2900A>C (p.Gln967Pro) c.900-4047A>C n.803A>C n.728A>C c.3059A>C (p.Gln1020Pro) c.*28+28372A>C (n.*28+28372A>C) c.2924A>C (p.Gln975Pro) c.2258A>C (p.Gln753Pro) | |
| 7 | g.55201300A>G | CA367582583 | EGFR | c.2900A>G (p.Gln967Arg) c.900-4047A>G n.803A>G n.728A>G c.3059A>G (p.Gln1020Arg) c.*28+28372A>G (n.*28+28372A>G) c.2924A>G (p.Gln975Arg) c.2258A>G (p.Gln753Arg) | |
| 7 | g.55201300A>T | CA367582584 | EGFR | c.2900A>T (p.Gln967Leu) c.900-4047A>T n.803A>T n.728A>T c.3059A>T (p.Gln1020Leu) c.*28+28372A>T (n.*28+28372A>T) c.2924A>T (p.Gln975Leu) c.2258A>T (p.Gln753Leu) | |
| 7 | g.55201301G>A | CA454968605 | EGFR | c.2901G>A (p.Gln967=) c.900-4046G>A n.804G>A n.729G>A c.3060G>A (p.Gln1020=) c.*28+28373G>A (n.*28+28373G>A) c.2925G>A (p.Gln975=) c.2259G>A (p.Gln753=) | ClinVar dbSNP |
| 7 | g.55201301G>C | CA367582586 | EGFR | c.2901G>C (p.Gln967His) c.900-4046G>C n.804G>C n.729G>C c.3060G>C (p.Gln1020His) c.*28+28373G>C (n.*28+28373G>C) c.2925G>C (p.Gln975His) c.2259G>C (p.Gln753His) | ClinVar dbSNP |
| 7 | g.55201301G>T | CA367582588 | EGFR | c.2901G>T (p.Gln967His) c.900-4046G>T n.804G>T n.729G>T c.3060G>T (p.Gln1020His) c.*28+28373G>T (n.*28+28373G>T) c.2925G>T (p.Gln975His) c.2259G>T (p.Gln753His) | dbSNP gnomAD v4 COSMIC |
| 7 | g.55201302del | CA2682856460 | EGFR | c.2902del (p.Gln968ArgfsTer15) c.900-4045del n.805del n.730del c.3061del (p.Gln1021ArgfsTer15) c.*28+28374del (n.*28+28374del) c.2926del (p.Gln976ArgfsTer15) c.2260del (p.Gln754ArgfsTer15) | gnomAD v4 |
| 7 | g.55201302C>A | CA367582590 | EGFR | c.2902C>A (p.Gln968Lys) c.900-4045C>A n.805C>A n.730C>A c.3061C>A (p.Gln1021Lys) c.*28+28374C>A (n.*28+28374C>A) c.2926C>A (p.Gln976Lys) c.2260C>A (p.Gln754Lys) | dbSNP |
| 7 | g.55201302C>G | CA367582592 | EGFR | c.2902C>G (p.Gln968Glu) c.900-4045C>G n.805C>G n.730C>G c.3061C>G (p.Gln1021Glu) c.*28+28374C>G (n.*28+28374C>G) c.2926C>G (p.Gln976Glu) c.2260C>G (p.Gln754Glu) | dbSNP |
| 7 | g.55201302C>T | CA367582594 | EGFR | c.2902C>T (p.Gln968Ter) c.900-4045C>T n.805C>T n.730C>T c.3061C>T (p.Gln1021Ter) c.*28+28374C>T (n.*28+28374C>T) c.2926C>T (p.Gln976Ter) c.2260C>T (p.Gln754Ter) | ClinVar dbSNP |
| 7 | g.55201303del | CA2682856461 | EGFR | c.2903del (p.Gln968ArgfsTer15) c.900-4044del n.806del n.731del c.3062del (p.Gln1021ArgfsTer15) c.*28+28375del (n.*28+28375del) c.2927del (p.Gln976ArgfsTer15) c.2261del (p.Gln754ArgfsTer15) | gnomAD v4 |
| 7 | g.55201303A>C | CA367582596 | EGFR | c.2903A>C (p.Gln968Pro) c.900-4044A>C n.806A>C n.731A>C c.3062A>C (p.Gln1021Pro) c.*28+28375A>C (n.*28+28375A>C) c.2927A>C (p.Gln976Pro) c.2261A>C (p.Gln754Pro) | |
| 7 | g.55201303A>G | CA367582598 | EGFR | c.2903A>G (p.Gln968Arg) c.900-4044A>G n.806A>G n.731A>G c.3062A>G (p.Gln1021Arg) c.*28+28375A>G (n.*28+28375A>G) c.2927A>G (p.Gln976Arg) c.2261A>G (p.Gln754Arg) | |
| 7 | g.55201303A>T | CA367582600 | EGFR | c.2903A>T (p.Gln968Leu) c.900-4044A>T n.806A>T n.731A>T c.3062A>T (p.Gln1021Leu) c.*28+28375A>T (n.*28+28375A>T) c.2927A>T (p.Gln976Leu) c.2261A>T (p.Gln754Leu) | gnomAD v4 |
| 7 | g.55201304G>A | CA454968616 | EGFR | c.2904G>A (p.Gln968=) c.900-4043G>A n.807G>A n.732G>A c.3063G>A (p.Gln1021=) c.*28+28376G>A (n.*28+28376G>A) c.2928G>A (p.Gln976=) c.2262G>A (p.Gln754=) | gnomAD v4 |
| 7 | g.55201304G>C | CA367582602 | EGFR | c.2904G>C (p.Gln968His) c.900-4043G>C n.807G>C n.732G>C c.3063G>C (p.Gln1021His) c.*28+28376G>C (n.*28+28376G>C) c.2928G>C (p.Gln976His) c.2262G>C (p.Gln754His) | |
| 7 | g.55201304G>T | CA367582604 | EGFR | c.2904G>T (p.Gln968His) c.900-4043G>T n.807G>T n.732G>T c.3063G>T (p.Gln1021His) c.*28+28376G>T (n.*28+28376G>T) c.2928G>T (p.Gln976His) c.2262G>T (p.Gln754His) | |
| 7 | g.55201305G>A | CA367582610 | EGFR | c.2905G>A (p.Gly969Ser) c.900-4042G>A n.808G>A n.733G>A c.3064G>A (p.Gly1022Ser) c.*28+28377G>A (n.*28+28377G>A) c.2929G>A (p.Gly977Ser) c.2263G>A (p.Gly755Ser) | dbSNP gnomAD v2 gnomAD v4 COSMIC |
| 7 | g.55201305G>C | CA367582608 | EGFR | c.2905G>C (p.Gly969Arg) c.900-4042G>C n.808G>C n.733G>C c.3064G>C (p.Gly1022Arg) c.*28+28377G>C (n.*28+28377G>C) c.2929G>C (p.Gly977Arg) c.2263G>C (p.Gly755Arg) | dbSNP |
| 7 | g.55201305G= | CA1708928464 | EGFR | c.2905G= (p.Gly969=) c.900-4042G= n.808G= n.733G= c.3064G= (p.Gly1022=) c.*28+28377G= (n.*28+28377G=) c.2929G= (p.Gly977=) c.2263G= (p.Gly755=) | |
| 7 | g.55201305G>T | CA367582607 | EGFR | c.2905G>T (p.Gly969Cys) c.900-4042G>T n.808G>T n.733G>T c.3064G>T (p.Gly1022Cys) c.*28+28377G>T (n.*28+28377G>T) c.2929G>T (p.Gly977Cys) c.2263G>T (p.Gly755Cys) | dbSNP gnomAD v4 |