Chr Mutation (hg38) CAid Gene Transcript Linkouts
7g.55191730C>ACA367580087EGFRc.2481C>A (p.Tyr827Ter)
c.*28+18802C>A (n.*28+18802C>A)
c.2346C>A (p.Tyr782Ter)
c.2322C>A (p.Tyr774Ter)
c.1680C>A (p.Tyr560Ter)
COSMIC
7g.55191730C>GCA367580088EGFRc.2481C>G (p.Tyr827Ter)
c.*28+18802C>G (n.*28+18802C>G)
c.2346C>G (p.Tyr782Ter)
c.2322C>G (p.Tyr774Ter)
c.1680C>G (p.Tyr560Ter)
7g.55191730C>TCA454965578EGFRc.2481C>T (p.Tyr827=)
c.*28+18802C>T (n.*28+18802C>T)
c.2346C>T (p.Tyr782=)
c.2322C>T (p.Tyr774=)
c.1680C>T (p.Tyr560=)
COSMIC
7g.55191731T>ACA367580089EGFRc.2482T>A (p.Leu828Met)
c.*28+18803T>A (n.*28+18803T>A)
c.2347T>A (p.Leu783Met)
c.2323T>A (p.Leu775Met)
c.1681T>A (p.Leu561Met)
7g.55191731T>CCA454965579EGFRc.2482T>C (p.Leu828=)
c.*28+18803T>C (n.*28+18803T>C)
c.2347T>C (p.Leu783=)
c.2323T>C (p.Leu775=)
c.1681T>C (p.Leu561=)
7g.55191731T>GCA367580090EGFRc.2482T>G (p.Leu828Val)
c.*28+18803T>G (n.*28+18803T>G)
c.2347T>G (p.Leu783Val)
c.2323T>G (p.Leu775Val)
c.1681T>G (p.Leu561Val)
7g.55191732T>ACA367580092EGFRc.2483T>A (p.Leu828Ter)
c.*28+18804T>A (n.*28+18804T>A)
c.2348T>A (p.Leu783Ter)
c.2324T>A (p.Leu775Ter)
c.1682T>A (p.Leu561Ter)
COSMIC
7g.55191732T>CCA367580093EGFRc.2483T>C (p.Leu828Ser)
c.*28+18804T>C (n.*28+18804T>C)
c.2348T>C (p.Leu783Ser)
c.2324T>C (p.Leu775Ser)
c.1682T>C (p.Leu561Ser)
7g.55191732T>GCA367580091EGFRc.2483T>G (p.Leu828Trp)
c.*28+18804T>G (n.*28+18804T>G)
c.2348T>G (p.Leu783Trp)
c.2324T>G (p.Leu775Trp)
c.1682T>G (p.Leu561Trp)
7g.55191733G>ACA180716EGFRc.2484G>A (p.Leu828=)
c.*28+18805G>A (n.*28+18805G>A)
c.2349G>A (p.Leu783=)
c.2325G>A (p.Leu775=)
c.1683G>A (p.Leu561=)
ClinVar dbSNP ExAC gnomAD COSMIC
7g.55191733G>CCA367580094EGFRc.2484G>C (p.Leu828Phe)
c.*28+18805G>C (n.*28+18805G>C)
c.2349G>C (p.Leu783Phe)
c.2325G>C (p.Leu775Phe)
c.1683G>C (p.Leu561Phe)
7g.55191733G=CA1708922405EGFRc.2484G= (p.Leu828=)
c.*28+18805G= (n.*28+18805G=)
c.2349G= (p.Leu783=)
c.2325G= (p.Leu775=)
c.1683G= (p.Leu561=)
7g.55191733G>TCA367580095EGFRc.2484G>T (p.Leu828Phe)
c.*28+18805G>T (n.*28+18805G>T)
c.2349G>T (p.Leu783Phe)
c.2325G>T (p.Leu775Phe)
c.1683G>T (p.Leu561Phe)
7g.55191734G>ACA367580096EGFRc.2485G>A (p.Glu829Lys)
c.*28+18806G>A (n.*28+18806G>A)
c.2350G>A (p.Glu784Lys)
c.2326G>A (p.Glu776Lys)
c.1684G>A (p.Glu562Lys)
COSMIC
7g.55191734G>CCA367580097EGFRc.2485G>C (p.Glu829Gln)
c.*28+18806G>C (n.*28+18806G>C)
c.2350G>C (p.Glu784Gln)
c.2326G>C (p.Glu776Gln)
c.1684G>C (p.Glu562Gln)
ClinVar
7g.55191734G=CA1708922413EGFRc.2485G= (p.Glu829=)
c.*28+18806G= (n.*28+18806G=)
c.2350G= (p.Glu784=)
c.2326G= (p.Glu776=)
c.1684G= (p.Glu562=)
7g.55191734G>TCA367580098EGFRc.2485G>T (p.Glu829Ter)
c.*28+18806G>T (n.*28+18806G>T)
c.2350G>T (p.Glu784Ter)
c.2326G>T (p.Glu776Ter)
c.1684G>T (p.Glu562Ter)
7g.55191735A>CCA367580101EGFRc.2486A>C (p.Glu829Ala)
c.*28+18807A>C (n.*28+18807A>C)
c.2351A>C (p.Glu784Ala)
c.2327A>C (p.Glu776Ala)
c.1685A>C (p.Glu562Ala)
7g.55191735A>GCA367580100EGFRc.2486A>G (p.Glu829Gly)
c.*28+18807A>G (n.*28+18807A>G)
c.2351A>G (p.Glu784Gly)
c.2327A>G (p.Glu776Gly)
c.1685A>G (p.Glu562Gly)
7g.55191735A>TCA367580099EGFRc.2486A>T (p.Glu829Val)
c.*28+18807A>T (n.*28+18807A>T)
c.2351A>T (p.Glu784Val)
c.2327A>T (p.Glu776Val)
c.1685A>T (p.Glu562Val)
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

Number of alleles fetched