Chr Mutation (hg38) CAid Gene Transcript Linkouts
7g.55191845G>ACA4266116EGFRc.2437G>A (p.Glu813Lys)
c.899+46G>A
c.2596G>A (p.Glu866Lys)
c.*28+18917G>A (n.*28+18917G>A)
c.2461G>A (p.Glu821Lys)
c.1795G>A (p.Glu599Lys)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC
7g.55191845G>CCA367580317EGFRc.2437G>C (p.Glu813Gln)
c.899+46G>C
c.2596G>C (p.Glu866Gln)
c.*28+18917G>C (n.*28+18917G>C)
c.2461G>C (p.Glu821Gln)
c.1795G>C (p.Glu599Gln)
COSMIC
7g.55191845G=CA1708922687EGFRc.2437G= (p.Glu813=)
c.899+46G=
c.2596G= (p.Glu866=)
c.*28+18917G= (n.*28+18917G=)
c.2461G= (p.Glu821=)
c.1795G= (p.Glu599=)
7g.55191845G>TCA367580316EGFRc.2437G>T (p.Glu813Ter)
c.899+46G>T
c.2596G>T (p.Glu866Ter)
c.*28+18917G>T (n.*28+18917G>T)
c.2461G>T (p.Glu821Ter)
c.1795G>T (p.Glu599Ter)
7g.55191846A=CA1708922693EGFRc.2438A= (p.Glu813=)
c.899+47A=
c.2597A= (p.Glu866=)
c.*28+18918A= (n.*28+18918A=)
c.2462A= (p.Glu821=)
c.1796A= (p.Glu599=)
7g.55191846A>CCA367580318EGFRc.2438A>C (p.Glu813Ala)
c.899+47A>C
c.2597A>C (p.Glu866Ala)
c.*28+18918A>C (n.*28+18918A>C)
c.2462A>C (p.Glu821Ala)
c.1796A>C (p.Glu599Ala)
gnomAD v4
7g.55191846A>GCA367580319EGFRc.2438A>G (p.Glu813Gly)
c.899+47A>G
c.2597A>G (p.Glu866Gly)
c.*28+18918A>G (n.*28+18918A>G)
c.2462A>G (p.Glu821Gly)
c.1796A>G (p.Glu599Gly)
dbSNP COSMIC
7g.55191846A>TCA135946EGFRc.2438A>T (p.Glu813Val)
c.899+47A>T
c.2597A>T (p.Glu866Val)
c.*28+18918A>T (n.*28+18918A>T)
c.2462A>T (p.Glu821Val)
c.1796A>T (p.Glu599Val)
ClinVar dbSNP COSMIC
7g.55191847G>ACA135949EGFRc.2439G>A (p.Glu813=)
c.899+48G>A
c.2598G>A (p.Glu866=)
c.*28+18919G>A (n.*28+18919G>A)
c.2463G>A (p.Glu821=)
c.1797G>A (p.Glu599=)
ClinVar dbSNP
7g.55191847G>CCA367580320EGFRc.2439G>C (p.Glu813Asp)
c.899+48G>C
c.2598G>C (p.Glu866Asp)
c.*28+18919G>C (n.*28+18919G>C)
c.2463G>C (p.Glu821Asp)
c.1797G>C (p.Glu599Asp)
dbSNP COSMIC
7g.55191847G=CA1708922700EGFRc.2439G= (p.Glu813=)
c.899+48G=
c.2598G= (p.Glu866=)
c.*28+18919G= (n.*28+18919G=)
c.2463G= (p.Glu821=)
c.1797G= (p.Glu599=)
7g.55191847G>TCA367580321EGFRc.2439G>T (p.Glu813Asp)
c.899+48G>T
c.2598G>T (p.Glu866Asp)
c.*28+18919G>T (n.*28+18919G>T)
c.2463G>T (p.Glu821Asp)
c.1797G>T (p.Glu599Asp)
COSMIC
7g.55191848A>CCA367580322EGFRc.2440A>C (p.Lys814Gln)
c.899+49A>C
c.2599A>C (p.Lys867Gln)
c.*28+18920A>C (n.*28+18920A>C)
c.2464A>C (p.Lys822Gln)
c.1798A>C (p.Lys600Gln)
7g.55191848A>GCA367580324EGFRc.2440A>G (p.Lys814Glu)
c.899+49A>G
c.2599A>G (p.Lys867Glu)
c.*28+18920A>G (n.*28+18920A>G)
c.2464A>G (p.Lys822Glu)
c.1798A>G (p.Lys600Glu)
dbSNP
7g.55191848A>TCA367580323EGFRc.2440A>T (p.Lys814Ter)
c.899+49A>T
c.2599A>T (p.Lys867Ter)
c.*28+18920A>T (n.*28+18920A>T)
c.2464A>T (p.Lys822Ter)
c.1798A>T (p.Lys600Ter)
7g.55191849A>CCA367580325EGFRc.2441A>C (p.Lys814Thr)
c.899+50A>C
c.2600A>C (p.Lys867Thr)
c.*28+18921A>C (n.*28+18921A>C)
c.2465A>C (p.Lys822Thr)
c.1799A>C (p.Lys600Thr)
7g.55191849A>GCA367580326EGFRc.2441A>G (p.Lys814Arg)
c.899+50A>G
c.2600A>G (p.Lys867Arg)
c.*28+18921A>G (n.*28+18921A>G)
c.2465A>G (p.Lys822Arg)
c.1799A>G (p.Lys600Arg)
dbSNP gnomAD v4
7g.55191849A>TCA367580327EGFRc.2441A>T (p.Lys814Ile)
c.899+50A>T
c.2600A>T (p.Lys867Ile)
c.*28+18921A>T (n.*28+18921A>T)
c.2465A>T (p.Lys822Ile)
c.1799A>T (p.Lys600Ile)
7g.55191850A>CCA367580328EGFRc.2442A>C (p.Lys814Asn)
c.899+51A>C
c.2601A>C (p.Lys867Asn)
c.*28+18922A>C (n.*28+18922A>C)
c.2466A>C (p.Lys822Asn)
c.1800A>C (p.Lys600Asn)
dbSNP
7g.55191850A>GCA454965667EGFRc.2442A>G (p.Lys814=)
c.899+51A>G
c.2601A>G (p.Lys867=)
c.*28+18922A>G (n.*28+18922A>G)
c.2466A>G (p.Lys822=)
c.1800A>G (p.Lys600=)
dbSNP
7g.55191850A>TCA367580329EGFRc.2442A>T (p.Lys814Asn)
c.899+51A>T
c.2601A>T (p.Lys867Asn)
c.*28+18922A>T (n.*28+18922A>T)
c.2466A>T (p.Lys822Asn)
c.1800A>T (p.Lys600Asn)
dbSNP
7g.55191851G>ACA269859EGFRc.2443G>A (p.Glu815Lys)
c.899+52G>A
c.2602G>A (p.Glu868Lys)
c.*28+18923G>A (n.*28+18923G>A)
c.2467G>A (p.Glu823Lys)
c.1801G>A (p.Glu601Lys)
ClinVar dbSNP gnomAD v3 gnomAD v4 COSMIC
7g.55191851G>CCA367580330EGFRc.2443G>C (p.Glu815Gln)
c.899+52G>C
c.2602G>C (p.Glu868Gln)
c.*28+18923G>C (n.*28+18923G>C)
c.2467G>C (p.Glu823Gln)
c.1801G>C (p.Glu601Gln)
dbSNP gnomAD v2
7g.55191851G=CA1708922712EGFRc.2443G= (p.Glu815=)
c.899+52G=
c.2602G= (p.Glu868=)
c.*28+18923G= (n.*28+18923G=)
c.2467G= (p.Glu823=)
c.1801G= (p.Glu601=)
7g.55191851G>TCA367580331EGFRc.2443G>T (p.Glu815Ter)
c.899+52G>T
c.2602G>T (p.Glu868Ter)
c.*28+18923G>T (n.*28+18923G>T)
c.2467G>T (p.Glu823Ter)
c.1801G>T (p.Glu601Ter)
7g.55191852A>CCA367580332EGFRc.2444A>C (p.Glu815Ala)
c.899+53A>C
c.2603A>C (p.Glu868Ala)
c.*28+18924A>C (n.*28+18924A>C)
c.2468A>C (p.Glu823Ala)
c.1802A>C (p.Glu601Ala)
7g.55191852A>GCA367580333EGFRc.2444A>G (p.Glu815Gly)
c.899+53A>G
c.2603A>G (p.Glu868Gly)
c.*28+18924A>G (n.*28+18924A>G)
c.2468A>G (p.Glu823Gly)
c.1802A>G (p.Glu601Gly)
dbSNP COSMIC
7g.55191852A>TCA367580334EGFRc.2444A>T (p.Glu815Val)
c.899+53A>T
c.2603A>T (p.Glu868Val)
c.*28+18924A>T (n.*28+18924A>T)
c.2468A>T (p.Glu823Val)
c.1802A>T (p.Glu601Val)
dbSNP COSMIC
7g.55191853A>CCA367580336EGFRc.2445A>C (p.Glu815Asp)
c.899+54A>C
c.2604A>C (p.Glu868Asp)
c.*28+18925A>C (n.*28+18925A>C)
c.2469A>C (p.Glu823Asp)
c.1803A>C (p.Glu601Asp)
dbSNP
7g.55191853A>GCA454965668EGFRc.2445A>G (p.Glu815=)
c.899+54A>G
c.2604A>G (p.Glu868=)
c.*28+18925A>G (n.*28+18925A>G)
c.2469A>G (p.Glu823=)
c.1803A>G (p.Glu601=)
ClinVar dbSNP gnomAD v4
7g.55191853A>TCA367580335EGFRc.2445A>T (p.Glu815Asp)
c.899+54A>T
c.2604A>T (p.Glu868Asp)
c.*28+18925A>T (n.*28+18925A>T)
c.2469A>T (p.Glu823Asp)
c.1803A>T (p.Glu601Asp)
COSMIC
7g.55191854T>ACA367580337EGFRc.2446T>A (p.Tyr816Asn)
c.899+55T>A
c.2605T>A (p.Tyr869Asn)
c.*28+18926T>A (n.*28+18926T>A)
c.2470T>A (p.Tyr824Asn)
c.1804T>A (p.Tyr602Asn)
dbSNP
7g.55191854T>CCA367580338EGFRc.2446T>C (p.Tyr816His)
c.899+55T>C
c.2605T>C (p.Tyr869His)
c.*28+18926T>C (n.*28+18926T>C)
c.2470T>C (p.Tyr824His)
c.1804T>C (p.Tyr602His)
ClinVar
7g.55191854T>GCA367580339EGFRc.2446T>G (p.Tyr816Asp)
c.899+55T>G
c.2605T>G (p.Tyr869Asp)
c.*28+18926T>G (n.*28+18926T>G)
c.2470T>G (p.Tyr824Asp)
c.1804T>G (p.Tyr602Asp)
7g.55191855A=CA1708922717EGFRc.2447A= (p.Tyr816=)
c.899+56A=
c.2606A= (p.Tyr869=)
c.*28+18927A= (n.*28+18927A=)
c.2471A= (p.Tyr824=)
c.1805A= (p.Tyr602=)
7g.55191855A>CCA367580340EGFRc.2447A>C (p.Tyr816Ser)
c.899+56A>C
c.2606A>C (p.Tyr869Ser)
c.*28+18927A>C (n.*28+18927A>C)
c.2471A>C (p.Tyr824Ser)
c.1805A>C (p.Tyr602Ser)
7g.55191855A>GCA367580341EGFRc.2447A>G (p.Tyr816Cys)
c.899+56A>G
c.2606A>G (p.Tyr869Cys)
c.*28+18927A>G (n.*28+18927A>G)
c.2471A>G (p.Tyr824Cys)
c.1805A>G (p.Tyr602Cys)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
7g.55191855A>TCA367580342EGFRc.2447A>T (p.Tyr816Phe)
c.899+56A>T
c.2606A>T (p.Tyr869Phe)
c.*28+18927A>T (n.*28+18927A>T)
c.2471A>T (p.Tyr824Phe)
c.1805A>T (p.Tyr602Phe)
7g.55191856C>ACA367580343EGFRc.2448C>A (p.Tyr816Ter)
c.899+57C>A
c.2607C>A (p.Tyr869Ter)
c.*28+18928C>A (n.*28+18928C>A)
c.2472C>A (p.Tyr824Ter)
c.1806C>A (p.Tyr602Ter)
7g.55191856C>GCA367580344EGFRc.2448C>G (p.Tyr816Ter)
c.899+57C>G
c.2607C>G (p.Tyr869Ter)
c.*28+18928C>G (n.*28+18928C>G)
c.2472C>G (p.Tyr824Ter)
c.1806C>G (p.Tyr602Ter)
7g.55191856C>TCA454965669EGFRc.2448C>T (p.Tyr816=)
c.899+57C>T
c.2607C>T (p.Tyr869=)
c.*28+18928C>T (n.*28+18928C>T)
c.2472C>T (p.Tyr824=)
c.1806C>T (p.Tyr602=)
ClinVar dbSNP
7g.55191857C>ACA367580345EGFRc.2449C>A (p.His817Asn)
c.899+58C>A
c.2608C>A (p.His870Asn)
c.*28+18929C>A (n.*28+18929C>A)
c.2473C>A (p.His825Asn)
c.1807C>A (p.His603Asn)
dbSNP
7g.55191857C>GCA367580346EGFRc.2449C>G (p.His817Asp)
c.899+58C>G
c.2608C>G (p.His870Asp)
c.*28+18929C>G (n.*28+18929C>G)
c.2473C>G (p.His825Asp)
c.1807C>G (p.His603Asp)
dbSNP
7g.55191857C>TCA367580347EGFRc.2449C>T (p.His817Tyr)
c.899+58C>T
c.2608C>T (p.His870Tyr)
c.*28+18929C>T (n.*28+18929C>T)
c.2473C>T (p.His825Tyr)
c.1807C>T (p.His603Tyr)
dbSNP COSMIC
7g.55191858A=CA1708922720EGFRc.2450A= (p.His817=)
c.899+59A=
c.2609A= (p.His870=)
c.*28+18930A= (n.*28+18930A=)
c.2474A= (p.His825=)
c.1808A= (p.His603=)
7g.55191858A>CCA367580348EGFRc.2450A>C (p.His817Pro)
c.899+59A>C
c.2609A>C (p.His870Pro)
c.*28+18930A>C (n.*28+18930A>C)
c.2474A>C (p.His825Pro)
c.1808A>C (p.His603Pro)
dbSNP
7g.55191858A>GCA367580349EGFRc.2450A>G (p.His817Arg)
c.899+59A>G
c.2609A>G (p.His870Arg)
c.*28+18930A>G (n.*28+18930A>G)
c.2474A>G (p.His825Arg)
c.1808A>G (p.His603Arg)
ClinVar dbSNP COSMIC
7g.55191858A>TCA367580350EGFRc.2450A>T (p.His817Leu)
c.899+59A>T
c.2609A>T (p.His870Leu)
c.*28+18930A>T (n.*28+18930A>T)
c.2474A>T (p.His825Leu)
c.1808A>T (p.His603Leu)
dbSNP
7g.55191859T>ACA367580352EGFRc.2451T>A (p.His817Gln)
c.899+60T>A
c.2610T>A (p.His870Gln)
c.*28+18931T>A (n.*28+18931T>A)
c.2475T>A (p.His825Gln)
c.1809T>A (p.His603Gln)
7g.55191859T>CCA454965670EGFRc.2451T>C (p.His817=)
c.899+60T>C
c.2610T>C (p.His870=)
c.*28+18931T>C (n.*28+18931T>C)
c.2475T>C (p.His825=)
c.1809T>C (p.His603=)
ClinVar dbSNP gnomAD v4

Number of alleles fetched