Chr Mutation (hg38) CAid Gene Transcript Linkouts
7g.55191736G>ACA4266101EGFRc.2487G>A (p.Glu829=)
c.*28+18808G>A (n.*28+18808G>A)
c.2352G>A (p.Glu784=)
c.2328G>A (p.Glu776=)
c.1686G>A (p.Glu562=)
ClinVar dbSNP ExAC gnomAD COSMIC
7g.55191736G>CCA367580102EGFRc.2487G>C (p.Glu829Asp)
c.*28+18808G>C (n.*28+18808G>C)
c.2352G>C (p.Glu784Asp)
c.2328G>C (p.Glu776Asp)
c.1686G>C (p.Glu562Asp)
7g.55191736G=CA1708922418EGFRc.2487G= (p.Glu829=)
c.*28+18808G= (n.*28+18808G=)
c.2352G= (p.Glu784=)
c.2328G= (p.Glu776=)
c.1686G= (p.Glu562=)
7g.55191736G>TCA367580103EGFRc.2487G>T (p.Glu829Asp)
c.*28+18808G>T (n.*28+18808G>T)
c.2352G>T (p.Glu784Asp)
c.2328G>T (p.Glu776Asp)
c.1686G>T (p.Glu562Asp)
7g.55191737G>ACA367580104EGFRc.2488G>A (p.Asp830Asn)
c.*28+18809G>A (n.*28+18809G>A)
c.2353G>A (p.Asp785Asn)
c.2329G>A (p.Asp777Asn)
c.1687G>A (p.Asp563Asn)
7g.55191737G>CCA367580105EGFRc.2488G>C (p.Asp830His)
c.*28+18809G>C (n.*28+18809G>C)
c.2353G>C (p.Asp785His)
c.2329G>C (p.Asp777His)
c.1687G>C (p.Asp563His)
7g.55191737G>TCA367580106EGFRc.2488G>T (p.Asp830Tyr)
c.*28+18809G>T (n.*28+18809G>T)
c.2353G>T (p.Asp785Tyr)
c.2329G>T (p.Asp777Tyr)
c.1687G>T (p.Asp563Tyr)
7g.55191738A>CCA367580109EGFRc.2489A>C (p.Asp830Ala)
c.*28+18810A>C (n.*28+18810A>C)
c.2354A>C (p.Asp785Ala)
c.2330A>C (p.Asp777Ala)
c.1688A>C (p.Asp563Ala)
7g.55191738A>GCA367580107EGFRc.2489A>G (p.Asp830Gly)
c.*28+18810A>G (n.*28+18810A>G)
c.2354A>G (p.Asp785Gly)
c.2330A>G (p.Asp777Gly)
c.1688A>G (p.Asp563Gly)
7g.55191738A>TCA367580108EGFRc.2489A>T (p.Asp830Val)
c.*28+18810A>T (n.*28+18810A>T)
c.2354A>T (p.Asp785Val)
c.2330A>T (p.Asp777Val)
c.1688A>T (p.Asp563Val)
7g.55191739C>ACA367580110EGFRc.2490C>A (p.Asp830Glu)
c.*28+18811C>A (n.*28+18811C>A)
c.2355C>A (p.Asp785Glu)
c.2331C>A (p.Asp777Glu)
c.1689C>A (p.Asp563Glu)
7g.55191739C>GCA367580111EGFRc.2490C>G (p.Asp830Glu)
c.*28+18811C>G (n.*28+18811C>G)
c.2355C>G (p.Asp785Glu)
c.2331C>G (p.Asp777Glu)
c.1689C>G (p.Asp563Glu)
7g.55191739C>TCA454965581EGFRc.2490C>T (p.Asp830=)
c.*28+18811C>T (n.*28+18811C>T)
c.2355C>T (p.Asp785=)
c.2331C>T (p.Asp777=)
c.1689C>T (p.Asp563=)
7g.55191740C>ACA367580112EGFRc.2491C>A (p.Arg831Ser)
c.*28+18812C>A (n.*28+18812C>A)
c.2356C>A (p.Arg786Ser)
c.2332C>A (p.Arg778Ser)
c.1690C>A (p.Arg564Ser)
7g.55191740C=CA1708922424EGFRc.2491C= (p.Arg831=)
c.*28+18812C= (n.*28+18812C=)
c.2356C= (p.Arg786=)
c.2332C= (p.Arg778=)
c.1690C= (p.Arg564=)
7g.55191740C>GCA367580113EGFRc.2491C>G (p.Arg831Gly)
c.*28+18812C>G (n.*28+18812C>G)
c.2356C>G (p.Arg786Gly)
c.2332C>G (p.Arg778Gly)
c.1690C>G (p.Arg564Gly)
7g.55191740C>TCA135911EGFRc.2491C>T (p.Arg831Cys)
c.*28+18812C>T (n.*28+18812C>T)
c.2356C>T (p.Arg786Cys)
c.2332C>T (p.Arg778Cys)
c.1690C>T (p.Arg564Cys)
ClinVar dbSNP ExAC gnomAD COSMIC
7g.55191741G>ACA4266102EGFRc.2492G>A (p.Arg831His)
c.*28+18813G>A (n.*28+18813G>A)
c.2357G>A (p.Arg786His)
c.2333G>A (p.Arg778His)
c.1691G>A (p.Arg564His)
ClinVar dbSNP ExAC gnomAD COSMIC
7g.55191741G>CCA367580114EGFRc.2492G>C (p.Arg831Pro)
c.*28+18813G>C (n.*28+18813G>C)
c.2357G>C (p.Arg786Pro)
c.2333G>C (p.Arg778Pro)
c.1691G>C (p.Arg564Pro)
7g.55191741G=CA1708922429EGFRc.2492G= (p.Arg831=)
c.*28+18813G= (n.*28+18813G=)
c.2357G= (p.Arg786=)
c.2333G= (p.Arg778=)
c.1691G= (p.Arg564=)
7g.55191741G>TCA367580115EGFRc.2492G>T (p.Arg831Leu)
c.*28+18813G>T (n.*28+18813G>T)
c.2357G>T (p.Arg786Leu)
c.2333G>T (p.Arg778Leu)
c.1691G>T (p.Arg564Leu)
7g.55191742T>ACA454965583EGFRc.2493T>A (p.Arg831=)
c.*28+18814T>A (n.*28+18814T>A)
c.2358T>A (p.Arg786=)
c.2334T>A (p.Arg778=)
c.1692T>A (p.Arg564=)
7g.55191742T>CCA4266103EGFRc.2493T>C (p.Arg831=)
c.*28+18814T>C (n.*28+18814T>C)
c.2358T>C (p.Arg786=)
c.2334T>C (p.Arg778=)
c.1692T>C (p.Arg564=)
ClinVar dbSNP ExAC gnomAD
7g.55191742T>GCA4266104EGFRc.2493T>G (p.Arg831=)
c.*28+18814T>G (n.*28+18814T>G)
c.2358T>G (p.Arg786=)
c.2334T>G (p.Arg778=)
c.1692T>G (p.Arg564=)
dbSNP ExAC gnomAD
7g.55191742T=CA1708922434EGFRc.2493T= (p.Arg831=)
c.*28+18814T= (n.*28+18814T=)
c.2358T= (p.Arg786=)
c.2334T= (p.Arg778=)
c.1692T= (p.Arg564=)
7g.55191743C>ACA367580116EGFRc.2494C>A (p.Arg832Ser)
c.*28+18815C>A (n.*28+18815C>A)
c.2359C>A (p.Arg787Ser)
c.2335C>A (p.Arg779Ser)
c.1693C>A (p.Arg565Ser)
7g.55191743C=CA1708922439EGFRc.2494C= (p.Arg832=)
c.*28+18815C= (n.*28+18815C=)
c.2359C= (p.Arg787=)
c.2335C= (p.Arg779=)
c.1693C= (p.Arg565=)
7g.55191743C>GCA367580117EGFRc.2494C>G (p.Arg832Gly)
c.*28+18815C>G (n.*28+18815C>G)
c.2359C>G (p.Arg787Gly)
c.2335C>G (p.Arg779Gly)
c.1693C>G (p.Arg565Gly)
7g.55191743C>TCA4266105EGFRc.2494C>T (p.Arg832Cys)
c.*28+18815C>T (n.*28+18815C>T)
c.2359C>T (p.Arg787Cys)
c.2335C>T (p.Arg779Cys)
c.1693C>T (p.Arg565Cys)
ClinVar dbSNP ExAC gnomAD COSMIC
7g.55191744G>ACA4266106EGFRc.2495G>A (p.Arg832His)
c.*28+18816G>A (n.*28+18816G>A)
c.2360G>A (p.Arg787His)
c.2336G>A (p.Arg779His)
c.1694G>A (p.Arg565His)
ClinVar dbSNP ExAC gnomAD COSMIC
7g.55191744G>CCA367580119EGFRc.2495G>C (p.Arg832Pro)
c.*28+18816G>C (n.*28+18816G>C)
c.2360G>C (p.Arg787Pro)
c.2336G>C (p.Arg779Pro)
c.1694G>C (p.Arg565Pro)
7g.55191744G=CA1708922443EGFRc.2495G= (p.Arg832=)
c.*28+18816G= (n.*28+18816G=)
c.2360G= (p.Arg787=)
c.2336G= (p.Arg779=)
c.1694G= (p.Arg565=)
7g.55191744G>TCA367580118EGFRc.2495G>T (p.Arg832Leu)
c.*28+18816G>T (n.*28+18816G>T)
c.2360G>T (p.Arg787Leu)
c.2336G>T (p.Arg779Leu)
c.1694G>T (p.Arg565Leu)
gnomAD COSMIC
7g.55191745C>ACA454965585EGFRc.2496C>A (p.Arg832=)
c.*28+18817C>A (n.*28+18817C>A)
c.2361C>A (p.Arg787=)
c.2337C>A (p.Arg779=)
c.1695C>A (p.Arg565=)
7g.55191745C>GCA454965587EGFRc.2496C>G (p.Arg832=)
c.*28+18817C>G (n.*28+18817C>G)
c.2361C>G (p.Arg787=)
c.2337C>G (p.Arg779=)
c.1695C>G (p.Arg565=)
7g.55191745C>TCA454965588EGFRc.2496C>T (p.Arg832=)
c.*28+18817C>T (n.*28+18817C>T)
c.2361C>T (p.Arg787=)
c.2337C>T (p.Arg779=)
c.1695C>T (p.Arg565=)
7g.55191746T>ACA367580120EGFRc.2497T>A (p.Leu833Met)
c.*28+18818T>A (n.*28+18818T>A)
c.2362T>A (p.Leu788Met)
c.2338T>A (p.Leu780Met)
c.1696T>A (p.Leu566Met)
7g.55191746T>CCA454965589EGFRc.2497T>C (p.Leu833=)
c.*28+18818T>C (n.*28+18818T>C)
c.2362T>C (p.Leu788=)
c.2338T>C (p.Leu780=)
c.1696T>C (p.Leu566=)
7g.55191746T>GCA135914EGFRc.2497T>G (p.Leu833Val)
c.*28+18818T>G (n.*28+18818T>G)
c.2362T>G (p.Leu788Val)
c.2338T>G (p.Leu780Val)
c.1696T>G (p.Leu566Val)
ClinVar dbSNP COSMIC
7g.55191746T=CA1708922450EGFRc.2497T= (p.Leu833=)
c.*28+18818T= (n.*28+18818T=)
c.2362T= (p.Leu788=)
c.2338T= (p.Leu780=)
c.1696T= (p.Leu566=)
7g.55191746_55191747delinsCCCA2573142232EGFRc.2497_2498delinsCC (p.Leu833Pro)
c.*28+18818_*28+18819delinsCC (n.*28+18818_*28+18819delinsCC)
c.2362_2363delinsCC (p.Leu788Pro)
c.2338_2339delinsCC (p.Leu780Pro)
c.1696_1697delinsCC (p.Leu566Pro)
ClinVar
7g.55191747T>ACA367580121EGFRc.2498T>A (p.Leu833Ter)
c.*28+18819T>A (n.*28+18819T>A)
c.2363T>A (p.Leu788Ter)
c.2339T>A (p.Leu780Ter)
c.1697T>A (p.Leu566Ter)
7g.55191747T>CCA367580122EGFRc.2498T>C (p.Leu833Ser)
c.*28+18819T>C (n.*28+18819T>C)
c.2363T>C (p.Leu788Ser)
c.2339T>C (p.Leu780Ser)
c.1697T>C (p.Leu566Ser)
7g.55191747T>GCA367580123EGFRc.2498T>G (p.Leu833Trp)
c.*28+18819T>G (n.*28+18819T>G)
c.2363T>G (p.Leu788Trp)
c.2339T>G (p.Leu780Trp)
c.1697T>G (p.Leu566Trp)
COSMIC
7g.55191747_55191748delinsTGCA1708922456EGFRc.2498_2499delinsTG (p.Leu833=)
c.*28+18819_*28+18820delinsTG (n.*28+18819_*28+18820delinsTG)
c.2363_2364delinsTG (p.Leu788=)
c.2339_2340delinsTG (p.Leu780=)
c.1697_1698delinsTG (p.Leu566=)
7g.55191747_55191835delinsTGGTGCACCGCGACCTGGCAGCCAGGAACGTACTGGTGAAAACACCGCAGCATGTCAAGATCACAGATTTTGGGCTGGCCAAACTGCTGCA1708922454EGFRc.2498_2586delinsTGGTGCACCGCGACCTGGCAGCCAGGAACGTACTGGTGAAAACACCGCAGCATGTCAAGATCACAGATTTTGGGCTGGCCAAACTGCTG (p.Leu833=)
c.*28+18819_*28+18907delinsTGGTGCACCGCGACCTGGCAGCCAGGAACGTACTGGTGAAAACACCGCAGCATGTCAAGATCACAGATTTTGGGCTGGCCAAACTGCTG (n.*28+18819_*28+18907delinsTGGTGCACCGCGACCTGGCAGCCAGGAACGTACTGGTGAAAACACCGCAGCATGTCAAGATCACAGATTTTGGGCTGGCCAAACTGCTG)
c.2363_2451delinsTGGTGCACCGCGACCTGGCAGCCAGGAACGTACTGGTGAAAACACCGCAGCATGTCAAGATCACAGATTTTGGGCTGGCCAAACTGCTG (p.Leu788=)
c.2339_2427delinsTGGTGCACCGCGACCTGGCAGCCAGGAACGTACTGGTGAAAACACCGCAGCATGTCAAGATCACAGATTTTGGGCTGGCCAAACTGCTG (p.Leu780=)
c.1697_1785delinsTGGTGCACCGCGACCTGGCAGCCAGGAACGTACTGGTGAAAACACCGCAGCATGTCAAGATCACAGATTTTGGGCTGGCCAAACTGCTG (p.Leu566=)
7g.55191748G>ACA454965593EGFRc.2499G>A (p.Leu833=)
c.*28+18820G>A (n.*28+18820G>A)
c.2364G>A (p.Leu788=)
c.2340G>A (p.Leu780=)
c.1698G>A (p.Leu566=)
7g.55191748G>CCA367580124EGFRc.2499G>C (p.Leu833Phe)
c.*28+18820G>C (n.*28+18820G>C)
c.2364G>C (p.Leu788Phe)
c.2340G>C (p.Leu780Phe)
c.1698G>C (p.Leu566Phe)
7g.55191748G>TCA367580125EGFRc.2499G>T (p.Leu833Phe)
c.*28+18820G>T (n.*28+18820G>T)
c.2364G>T (p.Leu788Phe)
c.2340G>T (p.Leu780Phe)
c.1698G>T (p.Leu566Phe)
COSMIC
7g.55191748_55191749delinsTTCA891842020EGFRc.2499_2500delinsTT (p.Leu833_Val834delinsPheLeu)
c.*28+18820_*28+18821delinsTT (n.*28+18820_*28+18821delinsTT)
c.2364_2365delinsTT (p.Leu788_Val789delinsPheLeu)
c.2340_2341delinsTT (p.Leu780_Val781delinsPheLeu)
c.1698_1699delinsTT (p.Leu566_Val567delinsPheLeu)

Number of alleles fetched