Chr Mutation (hg38) CAid Gene Transcript Linkouts
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.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.55191832G>ACA454965654EGFRc.2424G>A (p.Leu808=)
c.899+33G>A
c.2583G>A (p.Leu861=)
c.*28+18904G>A (n.*28+18904G>A)
c.2448G>A (p.Leu816=)
c.1782G>A (p.Leu594=)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
7g.55191832G>CCA454965655EGFRc.2424G>C (p.Leu808=)
c.899+33G>C
c.2583G>C (p.Leu861=)
c.*28+18904G>C (n.*28+18904G>C)
c.2448G>C (p.Leu816=)
c.1782G>C (p.Leu594=)
dbSNP gnomAD v4
7g.55191832G=CA1708922671EGFRc.2424G= (p.Leu808=)
c.899+33G=
c.2583G= (p.Leu861=)
c.*28+18904G= (n.*28+18904G=)
c.2448G= (p.Leu816=)
c.1782G= (p.Leu594=)
7g.55191832G>TCA454965656EGFRc.2424G>T (p.Leu808=)
c.899+33G>T
c.2583G>T (p.Leu861=)
c.*28+18904G>T (n.*28+18904G>T)
c.2448G>T (p.Leu816=)
c.1782G>T (p.Leu594=)
7g.55191833C>ACA367580293EGFRc.2425C>A (p.Leu809Met)
c.899+34C>A
c.2584C>A (p.Leu862Met)
c.*28+18905C>A (n.*28+18905C>A)
c.2449C>A (p.Leu817Met)
c.1783C>A (p.Leu595Met)
dbSNP
7g.55191833C>GCA367580292EGFRc.2425C>G (p.Leu809Val)
c.899+34C>G
c.2584C>G (p.Leu862Val)
c.*28+18905C>G (n.*28+18905C>G)
c.2449C>G (p.Leu817Val)
c.1783C>G (p.Leu595Val)
7g.55191833C>TCA454965657EGFRc.2425C>T (p.Leu809=)
c.899+34C>T
c.2584C>T (p.Leu862=)
c.*28+18905C>T (n.*28+18905C>T)
c.2449C>T (p.Leu817=)
c.1783C>T (p.Leu595=)
dbSNP gnomAD v4
7g.55191834T>ACA367580294EGFRc.2426T>A (p.Leu809Gln)
c.899+35T>A
c.2585T>A (p.Leu862Gln)
c.*28+18906T>A (n.*28+18906T>A)
c.2450T>A (p.Leu817Gln)
c.1784T>A (p.Leu595Gln)
COSMIC
7g.55191834T>CCA367580295EGFRc.2426T>C (p.Leu809Pro)
c.899+35T>C
c.2585T>C (p.Leu862Pro)
c.*28+18906T>C (n.*28+18906T>C)
c.2450T>C (p.Leu817Pro)
c.1784T>C (p.Leu595Pro)
gnomAD v4 COSMIC
7g.55191834T>GCA367580296EGFRc.2426T>G (p.Leu809Arg)
c.899+35T>G
c.2585T>G (p.Leu862Arg)
c.*28+18906T>G (n.*28+18906T>G)
c.2450T>G (p.Leu817Arg)
c.1784T>G (p.Leu595Arg)
COSMIC
7g.55191835G>ACA454965658EGFRc.2427G>A (p.Leu809=)
c.899+36G>A
c.2586G>A (p.Leu862=)
c.*28+18907G>A (n.*28+18907G>A)
c.2451G>A (p.Leu817=)
c.1785G>A (p.Leu595=)
dbSNP gnomAD v4
7g.55191835G>CCA454965659EGFRc.2427G>C (p.Leu809=)
c.899+36G>C
c.2586G>C (p.Leu862=)
c.*28+18907G>C (n.*28+18907G>C)
c.2451G>C (p.Leu817=)
c.1785G>C (p.Leu595=)
dbSNP
7g.55191835G>TCA454965660EGFRc.2427G>T (p.Leu809=)
c.899+36G>T
c.2586G>T (p.Leu862=)
c.*28+18907G>T (n.*28+18907G>T)
c.2451G>T (p.Leu817=)
c.1785G>T (p.Leu595=)
dbSNP
7g.55191836G>ACA367580297EGFRc.2428G>A (p.Gly810Ser)
c.899+37G>A
c.2587G>A (p.Gly863Ser)
c.*28+18908G>A (n.*28+18908G>A)
c.2452G>A (p.Gly818Ser)
c.1786G>A (p.Gly596Ser)
ClinVar dbSNP gnomAD v4 COSMIC
7g.55191836G>CCA367580298EGFRc.2428G>C (p.Gly810Arg)
c.899+37G>C
c.2587G>C (p.Gly863Arg)
c.*28+18908G>C (n.*28+18908G>C)
c.2452G>C (p.Gly818Arg)
c.1786G>C (p.Gly596Arg)
dbSNP
7g.55191836G>TCA367580299EGFRc.2428G>T (p.Gly810Cys)
c.899+37G>T
c.2587G>T (p.Gly863Cys)
c.*28+18908G>T (n.*28+18908G>T)
c.2452G>T (p.Gly818Cys)
c.1786G>T (p.Gly596Cys)
ClinVar dbSNP gnomAD v4
7g.55191837G>ACA158934272EGFRc.2429G>A (p.Gly810Asp)
c.899+38G>A
c.2588G>A (p.Gly863Asp)
c.*28+18909G>A (n.*28+18909G>A)
c.2453G>A (p.Gly818Asp)
c.1787G>A (p.Gly596Asp)
ClinVar dbSNP gnomAD v4 COSMIC
7g.55191837G>CCA367580300EGFRc.2429G>C (p.Gly810Ala)
c.899+38G>C
c.2588G>C (p.Gly863Ala)
c.*28+18909G>C (n.*28+18909G>C)
c.2453G>C (p.Gly818Ala)
c.1787G>C (p.Gly596Ala)
dbSNP
7g.55191837G=CA1708922675EGFRc.2429G= (p.Gly810=)
c.899+38G=
c.2588G= (p.Gly863=)
c.*28+18909G= (n.*28+18909G=)
c.2453G= (p.Gly818=)
c.1787G= (p.Gly596=)
7g.55191837G>TCA367580301EGFRc.2429G>T (p.Gly810Val)
c.899+38G>T
c.2588G>T (p.Gly863Val)
c.*28+18909G>T (n.*28+18909G>T)
c.2453G>T (p.Gly818Val)
c.1787G>T (p.Gly596Val)
COSMIC
7g.55191838T>ACA454965663EGFRc.2430T>A (p.Gly810=)
c.899+39T>A
c.2589T>A (p.Gly863=)
c.*28+18910T>A (n.*28+18910T>A)
c.2454T>A (p.Gly818=)
c.1788T>A (p.Gly596=)
dbSNP
7g.55191838T>CCA454965662EGFRc.2430T>C (p.Gly810=)
c.899+39T>C
c.2589T>C (p.Gly863=)
c.*28+18910T>C (n.*28+18910T>C)
c.2454T>C (p.Gly818=)
c.1788T>C (p.Gly596=)
7g.55191838T>GCA454965661EGFRc.2430T>G (p.Gly810=)
c.899+39T>G
c.2589T>G (p.Gly863=)
c.*28+18910T>G (n.*28+18910T>G)
c.2454T>G (p.Gly818=)
c.1788T>G (p.Gly596=)
dbSNP COSMIC
7g.55191839G>ACA367580302EGFRc.2431G>A (p.Ala811Thr)
c.899+40G>A
c.2590G>A (p.Ala864Thr)
c.*28+18911G>A (n.*28+18911G>A)
c.2455G>A (p.Ala819Thr)
c.1789G>A (p.Ala597Thr)
ClinVar dbSNP gnomAD v4 COSMIC
7g.55191839G>CCA367580303EGFRc.2431G>C (p.Ala811Pro)
c.899+40G>C
c.2590G>C (p.Ala864Pro)
c.*28+18911G>C (n.*28+18911G>C)
c.2455G>C (p.Ala819Pro)
c.1789G>C (p.Ala597Pro)
dbSNP
7g.55191839G=CA1708922678EGFRc.2431G= (p.Ala811=)
c.899+40G=
c.2590G= (p.Ala864=)
c.*28+18911G= (n.*28+18911G=)
c.2455G= (p.Ala819=)
c.1789G= (p.Ala597=)
7g.55191839G>TCA367580304EGFRc.2431G>T (p.Ala811Ser)
c.899+40G>T
c.2590G>T (p.Ala864Ser)
c.*28+18911G>T (n.*28+18911G>T)
c.2455G>T (p.Ala819Ser)
c.1789G>T (p.Ala597Ser)
dbSNP
7g.55191840C>ACA367580305EGFRc.2432C>A (p.Ala811Glu)
c.899+41C>A
c.2591C>A (p.Ala864Glu)
c.*28+18912C>A (n.*28+18912C>A)
c.2456C>A (p.Ala819Glu)
c.1790C>A (p.Ala597Glu)
dbSNP COSMIC
7g.55191840C>GCA367580306EGFRc.2432C>G (p.Ala811Gly)
c.899+41C>G
c.2591C>G (p.Ala864Gly)
c.*28+18912C>G (n.*28+18912C>G)
c.2456C>G (p.Ala819Gly)
c.1790C>G (p.Ala597Gly)
gnomAD v4
7g.55191840C>TCA367580307EGFRc.2432C>T (p.Ala811Val)
c.899+41C>T
c.2591C>T (p.Ala864Val)
c.*28+18912C>T (n.*28+18912C>T)
c.2456C>T (p.Ala819Val)
c.1790C>T (p.Ala597Val)
ClinVar dbSNP gnomAD v4 COSMIC
7g.55191841G>ACA135943EGFRc.2433G>A (p.Ala811=)
c.899+42G>A
c.2592G>A (p.Ala864=)
c.*28+18913G>A (n.*28+18913G>A)
c.2457G>A (p.Ala819=)
c.1791G>A (p.Ala597=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
7g.55191841G>CCA454965665EGFRc.2433G>C (p.Ala811=)
c.899+42G>C
c.2592G>C (p.Ala864=)
c.*28+18913G>C (n.*28+18913G>C)
c.2457G>C (p.Ala819=)
c.1791G>C (p.Ala597=)
dbSNP
7g.55191841G=CA1708922684EGFRc.2433G= (p.Ala811=)
c.899+42G=
c.2592G= (p.Ala864=)
c.*28+18913G= (n.*28+18913G=)
c.2457G= (p.Ala819=)
c.1791G= (p.Ala597=)
7g.55191841G>TCA454965664EGFRc.2433G>T (p.Ala811=)
c.899+42G>T
c.2592G>T (p.Ala864=)
c.*28+18913G>T (n.*28+18913G>T)
c.2457G>T (p.Ala819=)
c.1791G>T (p.Ala597=)
dbSNP gnomAD v4
7g.55191842G>ACA367580309EGFRc.2434G>A (p.Glu812Lys)
c.899+43G>A
c.2593G>A (p.Glu865Lys)
c.*28+18914G>A (n.*28+18914G>A)
c.2458G>A (p.Glu820Lys)
c.1792G>A (p.Glu598Lys)
ClinVar dbSNP gnomAD v4 COSMIC
7g.55191842G>CCA367580308EGFRc.2434G>C (p.Glu812Gln)
c.899+43G>C
c.2593G>C (p.Glu865Gln)
c.*28+18914G>C (n.*28+18914G>C)
c.2458G>C (p.Glu820Gln)
c.1792G>C (p.Glu598Gln)
dbSNP
7g.55191842G>TCA367580310EGFRc.2434G>T (p.Glu812Ter)
c.899+43G>T
c.2593G>T (p.Glu865Ter)
c.*28+18914G>T (n.*28+18914G>T)
c.2458G>T (p.Glu820Ter)
c.1792G>T (p.Glu598Ter)
7g.55191843A>CCA367580311EGFRc.2435A>C (p.Glu812Ala)
c.899+44A>C
c.2594A>C (p.Glu865Ala)
c.*28+18915A>C (n.*28+18915A>C)
c.2459A>C (p.Glu820Ala)
c.1793A>C (p.Glu598Ala)
7g.55191843A>GCA367580312EGFRc.2435A>G (p.Glu812Gly)
c.899+44A>G
c.2594A>G (p.Glu865Gly)
c.*28+18915A>G (n.*28+18915A>G)
c.2459A>G (p.Glu820Gly)
c.1793A>G (p.Glu598Gly)
dbSNP
7g.55191843A>TCA367580313EGFRc.2435A>T (p.Glu812Val)
c.899+44A>T
c.2594A>T (p.Glu865Val)
c.*28+18915A>T (n.*28+18915A>T)
c.2459A>T (p.Glu820Val)
c.1793A>T (p.Glu598Val)
dbSNP
7g.55191844A>CCA367580314EGFRc.2436A>C (p.Glu812Asp)
c.899+45A>C
c.2595A>C (p.Glu865Asp)
c.*28+18916A>C (n.*28+18916A>C)
c.2460A>C (p.Glu820Asp)
c.1794A>C (p.Glu598Asp)
7g.55191844A>GCA454965666EGFRc.2436A>G (p.Glu812=)
c.899+45A>G
c.2595A>G (p.Glu865=)
c.*28+18916A>G (n.*28+18916A>G)
c.2460A>G (p.Glu820=)
c.1794A>G (p.Glu598=)
ClinVar dbSNP gnomAD v4
7g.55191844A>TCA367580315EGFRc.2436A>T (p.Glu812Asp)
c.899+45A>T
c.2595A>T (p.Glu865Asp)
c.*28+18916A>T (n.*28+18916A>T)
c.2460A>T (p.Glu820Asp)
c.1794A>T (p.Glu598Asp)
dbSNP
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=)

Number of alleles fetched