| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 7 | g.55191740C>A | CA367580112 | EGFR | c.2332C>A (p.Arg778Ser) c.840C>A c.2491C>A (p.Arg831Ser) c.*28+18812C>A (n.*28+18812C>A) c.2356C>A (p.Arg786Ser) c.1690C>A (p.Arg564Ser) | dbSNP |
| 7 | g.55191740C= | CA1708922424 | EGFR | c.2332C= (p.Arg778=) c.840C= c.2491C= (p.Arg831=) c.*28+18812C= (n.*28+18812C=) c.2356C= (p.Arg786=) c.1690C= (p.Arg564=) | |
| 7 | g.55191740C>G | CA367580113 | EGFR | c.2332C>G (p.Arg778Gly) c.840C>G c.2491C>G (p.Arg831Gly) c.*28+18812C>G (n.*28+18812C>G) c.2356C>G (p.Arg786Gly) c.1690C>G (p.Arg564Gly) | dbSNP |
| 7 | g.55191740C>T | CA135911 | EGFR | c.2332C>T (p.Arg778Cys) c.840C>T c.2491C>T (p.Arg831Cys) c.*28+18812C>T (n.*28+18812C>T) c.2356C>T (p.Arg786Cys) c.1690C>T (p.Arg564Cys) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 7 | g.55191741G>A | CA4266102 | EGFR | c.2333G>A (p.Arg778His) c.841G>A c.2492G>A (p.Arg831His) c.*28+18813G>A (n.*28+18813G>A) c.2357G>A (p.Arg786His) c.1691G>A (p.Arg564His) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 7 | g.55191741G>C | CA367580114 | EGFR | c.2333G>C (p.Arg778Pro) c.841G>C c.2492G>C (p.Arg831Pro) c.*28+18813G>C (n.*28+18813G>C) c.2357G>C (p.Arg786Pro) c.1691G>C (p.Arg564Pro) | dbSNP |
| 7 | g.55191741G= | CA1708922429 | EGFR | c.2333G= (p.Arg778=) c.841G= c.2492G= (p.Arg831=) c.*28+18813G= (n.*28+18813G=) c.2357G= (p.Arg786=) c.1691G= (p.Arg564=) | |
| 7 | g.55191741G>T | CA367580115 | EGFR | c.2333G>T (p.Arg778Leu) c.841G>T c.2492G>T (p.Arg831Leu) c.*28+18813G>T (n.*28+18813G>T) c.2357G>T (p.Arg786Leu) c.1691G>T (p.Arg564Leu) | dbSNP |
| 7 | g.55191742T>A | CA454965583 | EGFR | c.2334T>A (p.Arg778=) c.842T>A c.2493T>A (p.Arg831=) c.*28+18814T>A (n.*28+18814T>A) c.2358T>A (p.Arg786=) c.1692T>A (p.Arg564=) | dbSNP |
| 7 | g.55191742T>C | CA4266103 | EGFR | c.2334T>C (p.Arg778=) c.842T>C c.2493T>C (p.Arg831=) c.*28+18814T>C (n.*28+18814T>C) c.2358T>C (p.Arg786=) c.1692T>C (p.Arg564=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 7 | g.55191742T>G | CA4266104 | EGFR | c.2334T>G (p.Arg778=) c.842T>G c.2493T>G (p.Arg831=) c.*28+18814T>G (n.*28+18814T>G) c.2358T>G (p.Arg786=) c.1692T>G (p.Arg564=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 7 | g.55191742T= | CA1708922434 | EGFR | c.2334T= (p.Arg778=) c.842T= c.2493T= (p.Arg831=) c.*28+18814T= (n.*28+18814T=) c.2358T= (p.Arg786=) c.1692T= (p.Arg564=) | |
| 7 | g.55191743C>A | CA367580116 | EGFR | c.2335C>A (p.Arg779Ser) c.843C>A c.2494C>A (p.Arg832Ser) c.*28+18815C>A (n.*28+18815C>A) c.2359C>A (p.Arg787Ser) c.1693C>A (p.Arg565Ser) | dbSNP |
| 7 | g.55191743C= | CA1708922439 | EGFR | c.2335C= (p.Arg779=) c.843C= c.2494C= (p.Arg832=) c.*28+18815C= (n.*28+18815C=) c.2359C= (p.Arg787=) c.1693C= (p.Arg565=) | |
| 7 | g.55191743C>G | CA367580117 | EGFR | c.2335C>G (p.Arg779Gly) c.843C>G c.2494C>G (p.Arg832Gly) c.*28+18815C>G (n.*28+18815C>G) c.2359C>G (p.Arg787Gly) c.1693C>G (p.Arg565Gly) | dbSNP |
| 7 | g.55191743C>T | CA4266105 | EGFR | c.2335C>T (p.Arg779Cys) c.843C>T c.2494C>T (p.Arg832Cys) c.*28+18815C>T (n.*28+18815C>T) c.2359C>T (p.Arg787Cys) c.1693C>T (p.Arg565Cys) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC |
| 7 | g.55191744G>A | CA4266106 | EGFR | c.2336G>A (p.Arg779His) c.844G>A c.2495G>A (p.Arg832His) c.*28+18816G>A (n.*28+18816G>A) c.2360G>A (p.Arg787His) c.1694G>A (p.Arg565His) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 7 | g.55191744G>C | CA367580119 | EGFR | c.2336G>C (p.Arg779Pro) c.844G>C c.2495G>C (p.Arg832Pro) c.*28+18816G>C (n.*28+18816G>C) c.2360G>C (p.Arg787Pro) c.1694G>C (p.Arg565Pro) | dbSNP gnomAD v4 |
| 7 | g.55191744G= | CA1708922443 | EGFR | c.2336G= (p.Arg779=) c.844G= c.2495G= (p.Arg832=) c.*28+18816G= (n.*28+18816G=) c.2360G= (p.Arg787=) c.1694G= (p.Arg565=) | |
| 7 | g.55191744G>T | CA367580118 | EGFR | c.2336G>T (p.Arg779Leu) c.844G>T c.2495G>T (p.Arg832Leu) c.*28+18816G>T (n.*28+18816G>T) c.2360G>T (p.Arg787Leu) c.1694G>T (p.Arg565Leu) | dbSNP gnomAD v2 gnomAD v4 COSMIC |
| 7 | g.55191745C>A | CA454965585 | EGFR | c.2337C>A (p.Arg779=) c.845C>A c.2496C>A (p.Arg832=) c.*28+18817C>A (n.*28+18817C>A) c.2361C>A (p.Arg787=) c.1695C>A (p.Arg565=) | dbSNP |
| 7 | g.55191745C>G | CA454965587 | EGFR | c.2337C>G (p.Arg779=) c.845C>G c.2496C>G (p.Arg832=) c.*28+18817C>G (n.*28+18817C>G) c.2361C>G (p.Arg787=) c.1695C>G (p.Arg565=) | dbSNP |
| 7 | g.55191745C>T | CA454965588 | EGFR | c.2337C>T (p.Arg779=) c.845C>T c.2496C>T (p.Arg832=) c.*28+18817C>T (n.*28+18817C>T) c.2361C>T (p.Arg787=) c.1695C>T (p.Arg565=) | ClinVar dbSNP |
| 7 | g.55191746T>A | CA367580120 | EGFR | c.2338T>A (p.Leu780Met) c.846T>A c.2497T>A (p.Leu833Met) c.*28+18818T>A (n.*28+18818T>A) c.2362T>A (p.Leu788Met) c.1696T>A (p.Leu566Met) | dbSNP |
| 7 | g.55191746T>C | CA454965589 | EGFR | c.2338T>C (p.Leu780=) c.846T>C c.2497T>C (p.Leu833=) c.*28+18818T>C (n.*28+18818T>C) c.2362T>C (p.Leu788=) c.1696T>C (p.Leu566=) | dbSNP |
| 7 | g.55191746T>G | CA135914 | EGFR | c.2338T>G (p.Leu780Val) c.846T>G c.2497T>G (p.Leu833Val) c.*28+18818T>G (n.*28+18818T>G) c.2362T>G (p.Leu788Val) c.1696T>G (p.Leu566Val) | ClinVar dbSNP COSMIC |
| 7 | g.55191746T= | CA1708922450 | EGFR | c.2338T= (p.Leu780=) c.846T= c.2497T= (p.Leu833=) c.*28+18818T= (n.*28+18818T=) c.2362T= (p.Leu788=) c.1696T= (p.Leu566=) | |
| 7 | g.55191746_55191747delinsCC | CA2573142232 | EGFR | c.2338_2339delinsCC (p.Leu780Pro) c.846_847delinsCC c.2497_2498delinsCC (p.Leu833Pro) c.*28+18818_*28+18819delinsCC (n.*28+18818_*28+18819delinsCC) c.2362_2363delinsCC (p.Leu788Pro) c.1696_1697delinsCC (p.Leu566Pro) | ClinVar dbSNP |
| 7 | g.55191747T>A | CA367580121 | EGFR | c.2339T>A (p.Leu780Ter) c.847T>A c.2498T>A (p.Leu833Ter) c.*28+18819T>A (n.*28+18819T>A) c.2363T>A (p.Leu788Ter) c.1697T>A (p.Leu566Ter) | dbSNP |
| 7 | g.55191747T>C | CA367580122 | EGFR | c.2339T>C (p.Leu780Ser) c.847T>C c.2498T>C (p.Leu833Ser) c.*28+18819T>C (n.*28+18819T>C) c.2363T>C (p.Leu788Ser) c.1697T>C (p.Leu566Ser) | |
| 7 | g.55191747T>G | CA367580123 | EGFR | c.2339T>G (p.Leu780Trp) c.847T>G c.2498T>G (p.Leu833Trp) c.*28+18819T>G (n.*28+18819T>G) c.2363T>G (p.Leu788Trp) c.1697T>G (p.Leu566Trp) | dbSNP COSMIC |
| 7 | g.55191747_55191748delinsTG | CA1708922456 | EGFR | c.2339_2340delinsTG (p.Leu780=) c.847_848delinsTG c.2498_2499delinsTG (p.Leu833=) c.*28+18819_*28+18820delinsTG (n.*28+18819_*28+18820delinsTG) c.2363_2364delinsTG (p.Leu788=) c.1697_1698delinsTG (p.Leu566=) | |
| 7 | g.55191747_55191835delinsTGGTGCACCGCGACCTGGCAGCCAGGAACGTACTGGTGAAAACACCGCAGCATGTCAAGATCACAGATTTTGGGCTGGCCAAACTGCTG | CA1708922454 | EGFR | c.2339_2427delinsTGGTGCACCGCGACCTGGCAGCCAGGAACGTACTGGTGAAAACACCGCAGCATGTCAAGATCACAGATTTTGGGCTGGCCAAACTGCTG (p.Leu780=) c.847_899+36delinsTGGTGCACCGCGACCTGGCAGCCAGGAACGTACTGGTGAAAACACCGCAGCATGTCAAGATCACAGATTTTGGGCTGGCCAAACTGCTG c.2498_2586delinsTGGTGCACCGCGACCTGGCAGCCAGGAACGTACTGGTGAAAACACCGCAGCATGTCAAGATCACAGATTTTGGGCTGGCCAAACTGCTG (p.Leu833=) c.*28+18819_*28+18907delinsTGGTGCACCGCGACCTGGCAGCCAGGAACGTACTGGTGAAAACACCGCAGCATGTCAAGATCACAGATTTTGGGCTGGCCAAACTGCTG (n.*28+18819_*28+18907delinsTGGTGCACCGCGACCTGGCAGCCAGGAACGTACTGGTGAAAACACCGCAGCATGTCAAGATCACAGATTTTGGGCTGGCCAAACTGCTG) c.2363_2451delinsTGGTGCACCGCGACCTGGCAGCCAGGAACGTACTGGTGAAAACACCGCAGCATGTCAAGATCACAGATTTTGGGCTGGCCAAACTGCTG (p.Leu788=) c.1697_1785delinsTGGTGCACCGCGACCTGGCAGCCAGGAACGTACTGGTGAAAACACCGCAGCATGTCAAGATCACAGATTTTGGGCTGGCCAAACTGCTG (p.Leu566=) | |
| 7 | g.55191748G>A | CA454965593 | EGFR | c.2340G>A (p.Leu780=) c.848G>A c.2499G>A (p.Leu833=) c.*28+18820G>A (n.*28+18820G>A) c.2364G>A (p.Leu788=) c.1698G>A (p.Leu566=) | dbSNP |
| 7 | g.55191748G>C | CA367580124 | EGFR | c.2340G>C (p.Leu780Phe) c.848G>C c.2499G>C (p.Leu833Phe) c.*28+18820G>C (n.*28+18820G>C) c.2364G>C (p.Leu788Phe) c.1698G>C (p.Leu566Phe) | dbSNP |
| 7 | g.55191748G>T | CA367580125 | EGFR | c.2340G>T (p.Leu780Phe) c.848G>T c.2499G>T (p.Leu833Phe) c.*28+18820G>T (n.*28+18820G>T) c.2364G>T (p.Leu788Phe) c.1698G>T (p.Leu566Phe) | dbSNP COSMIC |
| 7 | g.55191748_55191749delinsTT | CA891842020 | EGFR | c.2340_2341delinsTT (p.Leu780_Val781delinsPheLeu) c.848_849delinsTT c.2499_2500delinsTT (p.Leu833_Val834delinsPheLeu) c.*28+18820_*28+18821delinsTT (n.*28+18820_*28+18821delinsTT) c.2364_2365delinsTT (p.Leu788_Val789delinsPheLeu) c.1698_1699delinsTT (p.Leu566_Val567delinsPheLeu) | |
| 7 | g.55191749del | CA1708922465 | EGFR | c.2341del (p.Val781CysfsTer12) c.849del c.2500del (p.Val834CysfsTer12) c.*28+18821del (n.*28+18821del) c.2365del (p.Val789CysfsTer12) c.1699del (p.Val567CysfsTer12) | dbSNP |
| 7 | g.55191753_55191840del | CA176020 | EGFR | c.2345_2432del (p.His782ArgfsTer?) c.853_899+41del c.2504_2591del (p.His835ArgfsTer?) c.*28+18825_*28+18912del (n.*28+18825_*28+18912del) c.2369_2456del (p.His790ArgfsTer?) c.1703_1790del (p.His568ArgfsTer?) | ClinVar dbSNP |
| 7 | g.55191749G>A | CA367580126 | EGFR | c.2341G>A (p.Val781Met) c.849G>A c.2500G>A (p.Val834Met) c.*28+18821G>A (n.*28+18821G>A) c.2365G>A (p.Val789Met) c.1699G>A (p.Val567Met) | dbSNP COSMIC |
| 7 | g.55191749G>C | CA135917 | EGFR | c.2341G>C (p.Val781Leu) c.849G>C c.2500G>C (p.Val834Leu) c.*28+18821G>C (n.*28+18821G>C) c.2365G>C (p.Val789Leu) c.1699G>C (p.Val567Leu) | ClinVar dbSNP |
| 7 | g.55191749G= | CA1708922471 | EGFR | c.2341G= (p.Val781=) c.849G= c.2500G= (p.Val834=) c.*28+18821G= (n.*28+18821G=) c.2365G= (p.Val789=) c.1699G= (p.Val567=) | |
| 7 | g.55191749G>T | CA135920 | EGFR | c.2341G>T (p.Val781Leu) c.849G>T c.2500G>T (p.Val834Leu) c.*28+18821G>T (n.*28+18821G>T) c.2365G>T (p.Val789Leu) c.1699G>T (p.Val567Leu) | ClinVar dbSNP COSMIC |
| 7 | g.55191749_55191751delinsATT | CA2573051279 | EGFR | c.2341_2343delinsATT (p.Val781Ile) c.849_851delinsATT c.2500_2502delinsATT (p.Val834Ile) c.*28+18821_*28+18823delinsATT (n.*28+18821_*28+18823delinsATT) c.2365_2367delinsATT (p.Val789Ile) c.1699_1701delinsATT (p.Val567Ile) | |
| 7 | g.55191750T>A | CA367580127 | EGFR | c.2342T>A (p.Val781Glu) c.850T>A c.2501T>A (p.Val834Glu) c.*28+18822T>A (n.*28+18822T>A) c.2366T>A (p.Val789Glu) c.1700T>A (p.Val567Glu) | dbSNP |
| 7 | g.55191750T>C | CA367580128 | EGFR | c.2342T>C (p.Val781Ala) c.850T>C c.2501T>C (p.Val834Ala) c.*28+18822T>C (n.*28+18822T>C) c.2366T>C (p.Val789Ala) c.1700T>C (p.Val567Ala) | dbSNP COSMIC |
| 7 | g.55191750T>G | CA367580129 | EGFR | c.2342T>G (p.Val781Gly) c.850T>G c.2501T>G (p.Val834Gly) c.*28+18822T>G (n.*28+18822T>G) c.2366T>G (p.Val789Gly) c.1700T>G (p.Val567Gly) | dbSNP |
| 7 | g.55191751G>A | CA454965594 | EGFR | c.2343G>A (p.Val781=) c.851G>A c.2502G>A (p.Val834=) c.*28+18823G>A (n.*28+18823G>A) c.2367G>A (p.Val789=) c.1701G>A (p.Val567=) | dbSNP |
| 7 | g.55191751G>C | CA454965595 | EGFR | c.2343G>C (p.Val781=) c.851G>C c.2502G>C (p.Val834=) c.*28+18823G>C (n.*28+18823G>C) c.2367G>C (p.Val789=) c.1701G>C (p.Val567=) | dbSNP |
| 7 | g.55191751G>T | CA454965596 | EGFR | c.2343G>T (p.Val781=) c.851G>T c.2502G>T (p.Val834=) c.*28+18823G>T (n.*28+18823G>T) c.2367G>T (p.Val789=) c.1701G>T (p.Val567=) | gnomAD v4 |