Chr Mutation (hg38) CAid Gene Transcript Linkouts
7g.55191721C>ACA454965570EGFRc.2472C>A (p.Gly824=)
c.*28+18793C>A (p.=)
c.2337C>A (p.Gly779=)
c.2313C>A (p.Gly771=)
c.1671C>A (p.Gly557=)
COSMIC
7g.55191721C>GCA454965571EGFRc.2472C>G (p.Gly824=)
c.*28+18793C>G (p.=)
c.2337C>G (p.Gly779=)
c.2313C>G (p.Gly771=)
c.1671C>G (p.Gly557=)
7g.55191721C>TCA454965572EGFRc.2472C>T (p.Gly824=)
c.*28+18793C>T (p.=)
c.2337C>T (p.Gly779=)
c.2313C>T (p.Gly771=)
c.1671C>T (p.Gly557=)
7g.55191722A>CCA367580065EGFRc.2473A>C (p.Met825Leu)
c.*28+18794A>C (p.=)
c.2338A>C (p.Met780Leu)
c.2314A>C (p.Met772Leu)
c.1672A>C (p.Met558Leu)
7g.55191722A>GCA367580066EGFRc.2473A>G (p.Met825Val)
c.*28+18794A>G (p.=)
c.2338A>G (p.Met780Val)
c.2314A>G (p.Met772Val)
c.1672A>G (p.Met558Val)
7g.55191722A>TCA367580067EGFRc.2473A>T (p.Met825Leu)
c.*28+18794A>T (p.=)
c.2338A>T (p.Met780Leu)
c.2314A>T (p.Met772Leu)
c.1672A>T (p.Met558Leu)
7g.55191723T>ACA367580068EGFRc.2474T>A (p.Met825Lys)
c.*28+18795T>A (p.=)
c.2339T>A (p.Met780Lys)
c.2315T>A (p.Met772Lys)
c.1673T>A (p.Met558Lys)
7g.55191723T>CCA367580069EGFRc.2474T>C (p.Met825Thr)
c.*28+18795T>C (p.=)
c.2339T>C (p.Met780Thr)
c.2315T>C (p.Met772Thr)
c.1673T>C (p.Met558Thr)
7g.55191723T>GCA367580070EGFRc.2474T>G (p.Met825Arg)
c.*28+18795T>G (p.=)
c.2339T>G (p.Met780Arg)
c.2315T>G (p.Met772Arg)
c.1673T>G (p.Met558Arg)
7g.55191724G>ACA367580071EGFRc.2475G>A (p.Met825Ile)
c.*28+18796G>A (p.=)
c.2340G>A (p.Met780Ile)
c.2316G>A (p.Met772Ile)
c.1674G>A (p.Met558Ile)
COSMIC
7g.55191724G>CCA367580072EGFRc.2475G>C (p.Met825Ile)
c.*28+18796G>C (p.=)
c.2340G>C (p.Met780Ile)
c.2316G>C (p.Met772Ile)
c.1674G>C (p.Met558Ile)
7g.55191724G=CA1708922388EGFRc.2475G= (p.Met825=)
c.*28+18796G= (p.=)
c.2340G= (p.Met780=)
c.2316G= (p.Met772=)
c.1674G= (p.Met558=)
7g.55191724G>TCA367580073EGFRc.2475G>T (p.Met825Ile)
c.*28+18796G>T (p.=)
c.2340G>T (p.Met780Ile)
c.2316G>T (p.Met772Ile)
c.1674G>T (p.Met558Ile)
COSMIC
7g.55191725A>CCA367580074EGFRc.2476A>C (p.Asn826His)
c.*28+18797A>C (p.=)
c.2341A>C (p.Asn781His)
c.2317A>C (p.Asn773His)
c.1675A>C (p.Asn559His)
7g.55191725A>GCA367580075EGFRc.2476A>G (p.Asn826Asp)
c.*28+18797A>G (p.=)
c.2341A>G (p.Asn781Asp)
c.2317A>G (p.Asn773Asp)
c.1675A>G (p.Asn559Asp)
7g.55191725A>TCA367580076EGFRc.2476A>T (p.Asn826Tyr)
c.*28+18797A>T (p.=)
c.2341A>T (p.Asn781Tyr)
c.2317A>T (p.Asn773Tyr)
c.1675A>T (p.Asn559Tyr)
7g.55191726A>CCA367580079EGFRc.2477A>C (p.Asn826Thr)
c.*28+18798A>C (p.=)
c.2342A>C (p.Asn781Thr)
c.2318A>C (p.Asn773Thr)
c.1676A>C (p.Asn559Thr)
7g.55191726A>GCA367580077EGFRc.2477A>G (p.Asn826Ser)
c.*28+18798A>G (p.=)
c.2342A>G (p.Asn781Ser)
c.2318A>G (p.Asn773Ser)
c.1676A>G (p.Asn559Ser)
COSMIC
7g.55191726A>TCA367580078EGFRc.2477A>T (p.Asn826Ile)
c.*28+18798A>T (p.=)
c.2342A>T (p.Asn781Ile)
c.2318A>T (p.Asn773Ile)
c.1676A>T (p.Asn559Ile)
7g.55191727C>ACA367580080EGFRc.2478C>A (p.Asn826Lys)
c.*28+18799C>A (p.=)
c.2343C>A (p.Asn781Lys)
c.2319C>A (p.Asn773Lys)
c.1677C>A (p.Asn559Lys)
7g.55191727C>GCA367580081EGFRc.2478C>G (p.Asn826Lys)
c.*28+18799C>G (p.=)
c.2343C>G (p.Asn781Lys)
c.2319C>G (p.Asn773Lys)
c.1677C>G (p.Asn559Lys)
7g.55191727C>TCA454965576EGFRc.2478C>T (p.Asn826=)
c.*28+18799C>T (p.=)
c.2343C>T (p.Asn781=)
c.2319C>T (p.Asn773=)
c.1677C>T (p.Asn559=)
7g.55191728T>ACA367580082EGFRc.2479T>A (p.Tyr827Asn)
c.*28+18800T>A (p.=)
c.2344T>A (p.Tyr782Asn)
c.2320T>A (p.Tyr774Asn)
c.1678T>A (p.Tyr560Asn)
7g.55191728T>CCA367580083EGFRc.2479T>C (p.Tyr827His)
c.*28+18800T>C (p.=)
c.2344T>C (p.Tyr782His)
c.2320T>C (p.Tyr774His)
c.1678T>C (p.Tyr560His)
7g.55191728T>GCA367580084EGFRc.2479T>G (p.Tyr827Asp)
c.*28+18800T>G (p.=)
c.2344T>G (p.Tyr782Asp)
c.2320T>G (p.Tyr774Asp)
c.1678T>G (p.Tyr560Asp)
7g.55191728T=CA1708922393EGFRc.2479T= (p.Tyr827=)
c.*28+18800T= (p.=)
c.2344T= (p.Tyr782=)
c.2320T= (p.Tyr774=)
c.1678T= (p.Tyr560=)
7g.55191729A=CA1708922398EGFRc.2480A= (p.Tyr827=)
c.*28+18801A= (p.=)
c.2345A= (p.Tyr782=)
c.2321A= (p.Tyr774=)
c.1679A= (p.Tyr560=)
7g.55191729A>CCA367580085EGFRc.2480A>C (p.Tyr827Ser)
c.*28+18801A>C (p.=)
c.2345A>C (p.Tyr782Ser)
c.2321A>C (p.Tyr774Ser)
c.1679A>C (p.Tyr560Ser)
7g.55191729A>GCA367580086EGFRc.2480A>G (p.Tyr827Cys)
c.*28+18801A>G (p.=)
c.2345A>G (p.Tyr782Cys)
c.2321A>G (p.Tyr774Cys)
c.1679A>G (p.Tyr560Cys)
7g.55191729A>TCA158934114EGFRc.2480A>T (p.Tyr827Phe)
c.*28+18801A>T (p.=)
c.2345A>T (p.Tyr782Phe)
c.2321A>T (p.Tyr774Phe)
c.1679A>T (p.Tyr560Phe)
dbSNP
7g.55191730C>ACA367580087EGFRc.2481C>A (p.Tyr827Ter)
c.*28+18802C>A (p.=)
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 (p.=)
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 (p.=)
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 (p.=)
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 (p.=)
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 (p.=)
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 (p.=)
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 (p.=)
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 (p.=)
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 (p.=)
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 (p.=)
c.2349G>C (p.Leu783Phe)
c.2325G>C (p.Leu775Phe)
c.1683G>C (p.Leu561Phe)
7g.55191733G=CA1708922405EGFRc.2484G= (p.Leu828=)
c.*28+18805G= (p.=)
c.2349G= (p.Leu783=)
c.2325G= (p.Leu775=)
c.1683G= (p.Leu561=)
7g.55191733G>TCA367580095EGFRc.2484G>T (p.Leu828Phe)
c.*28+18805G>T (p.=)
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 (p.=)
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 (p.=)
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= (p.=)
c.2350G= (p.Glu784=)
c.2326G= (p.Glu776=)
c.1684G= (p.Glu562=)
7g.55191734G>TCA367580098EGFRc.2485G>T (p.Glu829Ter)
c.*28+18806G>T (p.=)
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 (p.=)
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 (p.=)
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 (p.=)
c.2351A>T (p.Glu784Val)
c.2327A>T (p.Glu776Val)
c.1685A>T (p.Glu562Val)

Number of alleles fetched