Chr Mutation (hg38) CAid Gene Transcript Linkouts
7g.55191740C>ACA367580112EGFRc.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
7g.55191740C=CA1708922424EGFRc.2332C= (p.Arg778=)
c.840C=
c.2491C= (p.Arg831=)
c.*28+18812C= (n.*28+18812C=)
c.2356C= (p.Arg786=)
c.1690C= (p.Arg564=)
7g.55191740C>GCA367580113EGFRc.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
7g.55191740C>TCA135911EGFRc.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
7g.55191741G>ACA4266102EGFRc.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
7g.55191741G>CCA367580114EGFRc.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
7g.55191741G=CA1708922429EGFRc.2333G= (p.Arg778=)
c.841G=
c.2492G= (p.Arg831=)
c.*28+18813G= (n.*28+18813G=)
c.2357G= (p.Arg786=)
c.1691G= (p.Arg564=)
7g.55191741G>TCA367580115EGFRc.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
7g.55191742T>ACA454965583EGFRc.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
7g.55191742T>CCA4266103EGFRc.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
7g.55191742T>GCA4266104EGFRc.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
7g.55191742T=CA1708922434EGFRc.2334T= (p.Arg778=)
c.842T=
c.2493T= (p.Arg831=)
c.*28+18814T= (n.*28+18814T=)
c.2358T= (p.Arg786=)
c.1692T= (p.Arg564=)
7g.55191743C>ACA367580116EGFRc.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
7g.55191743C=CA1708922439EGFRc.2335C= (p.Arg779=)
c.843C=
c.2494C= (p.Arg832=)
c.*28+18815C= (n.*28+18815C=)
c.2359C= (p.Arg787=)
c.1693C= (p.Arg565=)
7g.55191743C>GCA367580117EGFRc.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
7g.55191743C>TCA4266105EGFRc.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
7g.55191744G>ACA4266106EGFRc.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
7g.55191744G>CCA367580119EGFRc.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
7g.55191744G=CA1708922443EGFRc.2336G= (p.Arg779=)
c.844G=
c.2495G= (p.Arg832=)
c.*28+18816G= (n.*28+18816G=)
c.2360G= (p.Arg787=)
c.1694G= (p.Arg565=)
7g.55191744G>TCA367580118EGFRc.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
7g.55191745C>ACA454965585EGFRc.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
7g.55191745C>GCA454965587EGFRc.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
7g.55191745C>TCA454965588EGFRc.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=)
dbSNP
7g.55191746T>ACA367580120EGFRc.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
7g.55191746T>CCA454965589EGFRc.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
7g.55191746T>GCA135914EGFRc.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
7g.55191746T=CA1708922450EGFRc.2338T= (p.Leu780=)
c.846T=
c.2497T= (p.Leu833=)
c.*28+18818T= (n.*28+18818T=)
c.2362T= (p.Leu788=)
c.1696T= (p.Leu566=)
7g.55191746_55191747delinsCCCA2573142232EGFRc.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
7g.55191747T>ACA367580121EGFRc.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
7g.55191747T>CCA367580122EGFRc.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)
7g.55191747T>GCA367580123EGFRc.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
7g.55191747_55191748delinsTGCA1708922456EGFRc.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=)
7g.55191747_55191835delinsTGGTGCACCGCGACCTGGCAGCCAGGAACGTACTGGTGAAAACACCGCAGCATGTCAAGATCACAGATTTTGGGCTGGCCAAACTGCTGCA1708922454EGFRc.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=)
7g.55191748G>ACA454965593EGFRc.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
7g.55191748G>CCA367580124EGFRc.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
7g.55191748G>TCA367580125EGFRc.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
7g.55191748_55191749delinsTTCA891842020EGFRc.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)
7g.55191749delCA1708922465EGFRc.2341del (p.Val781CysfsTer12)
c.849del
c.2500del (p.Val834CysfsTer12)
c.*28+18821del (n.*28+18821del)
c.2365del (p.Val789CysfsTer12)
c.1699del (p.Val567CysfsTer12)
dbSNP
7g.55191753_55191840delCA176020EGFRc.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
7g.55191749G>ACA367580126EGFRc.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
7g.55191749G>CCA135917EGFRc.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
7g.55191749G=CA1708922471EGFRc.2341G= (p.Val781=)
c.849G=
c.2500G= (p.Val834=)
c.*28+18821G= (n.*28+18821G=)
c.2365G= (p.Val789=)
c.1699G= (p.Val567=)
7g.55191749G>TCA135920EGFRc.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
7g.55191749_55191751delinsATTCA2573051279EGFRc.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)
7g.55191750T>ACA367580127EGFRc.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
7g.55191750T>CCA367580128EGFRc.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
7g.55191750T>GCA367580129EGFRc.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
7g.55191751G>ACA454965594EGFRc.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
7g.55191751G>CCA454965595EGFRc.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
7g.55191751G>TCA454965596EGFRc.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

Number of alleles fetched