Chr Mutation (hg38) CAid Gene Transcript Linkouts
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)
7g.55191749delCA1708922465EGFRc.2500del (p.Val834CysfsTer12)
c.*28+18821del (n.*28+18821del)
c.2365del (p.Val789CysfsTer12)
c.2341del (p.Val781CysfsTer12)
c.1699del (p.Val567CysfsTer12)
dbSNP
7g.55191753_55191840delCA176020EGFRc.2504_2591del (p.His835ArgfsTer?)
c.*28+18825_*28+18912del (n.*28+18825_*28+18912del)
c.2369_2456del (p.His790ArgfsTer?)
c.2345_2432del (p.His782ArgfsTer?)
c.1703_1790del (p.His568ArgfsTer?)
ClinVar dbSNP
7g.55191749G>ACA367580126EGFRc.2500G>A (p.Val834Met)
c.*28+18821G>A (n.*28+18821G>A)
c.2365G>A (p.Val789Met)
c.2341G>A (p.Val781Met)
c.1699G>A (p.Val567Met)
COSMIC
7g.55191749G>CCA135917EGFRc.2500G>C (p.Val834Leu)
c.*28+18821G>C (n.*28+18821G>C)
c.2365G>C (p.Val789Leu)
c.2341G>C (p.Val781Leu)
c.1699G>C (p.Val567Leu)
ClinVar dbSNP
7g.55191749G=CA1708922471EGFRc.2500G= (p.Val834=)
c.*28+18821G= (n.*28+18821G=)
c.2365G= (p.Val789=)
c.2341G= (p.Val781=)
c.1699G= (p.Val567=)
7g.55191749G>TCA135920EGFRc.2500G>T (p.Val834Leu)
c.*28+18821G>T (n.*28+18821G>T)
c.2365G>T (p.Val789Leu)
c.2341G>T (p.Val781Leu)
c.1699G>T (p.Val567Leu)
ClinVar dbSNP COSMIC
7g.55191749_55191751delinsATTCA2573051279EGFRc.2500_2502delinsATT (p.Val834Ile)
c.*28+18821_*28+18823delinsATT (n.*28+18821_*28+18823delinsATT)
c.2365_2367delinsATT (p.Val789Ile)
c.2341_2343delinsATT (p.Val781Ile)
c.1699_1701delinsATT (p.Val567Ile)
7g.55191750T>ACA367580127EGFRc.2501T>A (p.Val834Glu)
c.*28+18822T>A (n.*28+18822T>A)
c.2366T>A (p.Val789Glu)
c.2342T>A (p.Val781Glu)
c.1700T>A (p.Val567Glu)
7g.55191750T>CCA367580128EGFRc.2501T>C (p.Val834Ala)
c.*28+18822T>C (n.*28+18822T>C)
c.2366T>C (p.Val789Ala)
c.2342T>C (p.Val781Ala)
c.1700T>C (p.Val567Ala)
COSMIC
7g.55191750T>GCA367580129EGFRc.2501T>G (p.Val834Gly)
c.*28+18822T>G (n.*28+18822T>G)
c.2366T>G (p.Val789Gly)
c.2342T>G (p.Val781Gly)
c.1700T>G (p.Val567Gly)
7g.55191751G>ACA454965594EGFRc.2502G>A (p.Val834=)
c.*28+18823G>A (n.*28+18823G>A)
c.2367G>A (p.Val789=)
c.2343G>A (p.Val781=)
c.1701G>A (p.Val567=)
7g.55191751G>CCA454965595EGFRc.2502G>C (p.Val834=)
c.*28+18823G>C (n.*28+18823G>C)
c.2367G>C (p.Val789=)
c.2343G>C (p.Val781=)
c.1701G>C (p.Val567=)
7g.55191751G>TCA454965596EGFRc.2502G>T (p.Val834=)
c.*28+18823G>T (n.*28+18823G>T)
c.2367G>T (p.Val789=)
c.2343G>T (p.Val781=)
c.1701G>T (p.Val567=)
7g.55191752C>ACA367580132EGFRc.2503C>A (p.His835Asn)
c.*28+18824C>A (n.*28+18824C>A)
c.2368C>A (p.His790Asn)
c.2344C>A (p.His782Asn)
c.1702C>A (p.His568Asn)
7g.55191752C>GCA367580130EGFRc.2503C>G (p.His835Asp)
c.*28+18824C>G (n.*28+18824C>G)
c.2368C>G (p.His790Asp)
c.2344C>G (p.His782Asp)
c.1702C>G (p.His568Asp)
7g.55191752C>TCA367580131EGFRc.2503C>T (p.His835Tyr)
c.*28+18824C>T (n.*28+18824C>T)
c.2368C>T (p.His790Tyr)
c.2344C>T (p.His782Tyr)
c.1702C>T (p.His568Tyr)
7g.55191753A=CA1708922475EGFRc.2504A= (p.His835=)
c.*28+18825A= (n.*28+18825A=)
c.2369A= (p.His790=)
c.2345A= (p.His782=)
c.1703A= (p.His568=)
7g.55191753A>CCA367580133EGFRc.2504A>C (p.His835Pro)
c.*28+18825A>C (n.*28+18825A>C)
c.2369A>C (p.His790Pro)
c.2345A>C (p.His782Pro)
c.1703A>C (p.His568Pro)
7g.55191753A>GCA367580134EGFRc.2504A>G (p.His835Arg)
c.*28+18825A>G (n.*28+18825A>G)
c.2369A>G (p.His790Arg)
c.2345A>G (p.His782Arg)
c.1703A>G (p.His568Arg)
7g.55191753A>TCA135921EGFRc.2504A>T (p.His835Leu)
c.*28+18825A>T (n.*28+18825A>T)
c.2369A>T (p.His790Leu)
c.2345A>T (p.His782Leu)
c.1703A>T (p.His568Leu)
ClinVar dbSNP COSMIC
7g.55191754C>ACA367580135EGFRc.2505C>A (p.His835Gln)
c.*28+18826C>A (n.*28+18826C>A)
c.2370C>A (p.His790Gln)
c.2346C>A (p.His782Gln)
c.1704C>A (p.His568Gln)
7g.55191754C>GCA367580136EGFRc.2505C>G (p.His835Gln)
c.*28+18826C>G (n.*28+18826C>G)
c.2370C>G (p.His790Gln)
c.2346C>G (p.His782Gln)
c.1704C>G (p.His568Gln)
7g.55191754C>TCA454965597EGFRc.2505C>T (p.His835=)
c.*28+18826C>T (n.*28+18826C>T)
c.2370C>T (p.His790=)
c.2346C>T (p.His782=)
c.1704C>T (p.His568=)
COSMIC
7g.55191755C>ACA367580137EGFRc.2506C>A (p.Arg836Ser)
c.*28+18827C>A (n.*28+18827C>A)
c.2371C>A (p.Arg791Ser)
c.2347C>A (p.Arg783Ser)
c.1705C>A (p.Arg569Ser)
COSMIC
7g.55191755C=CA1708922481EGFRc.2506C= (p.Arg836=)
c.*28+18827C= (n.*28+18827C=)
c.2371C= (p.Arg791=)
c.2347C= (p.Arg783=)
c.1705C= (p.Arg569=)
7g.55191755C>GCA367580138EGFRc.2506C>G (p.Arg836Gly)
c.*28+18827C>G (n.*28+18827C>G)
c.2371C>G (p.Arg791Gly)
c.2347C>G (p.Arg783Gly)
c.1705C>G (p.Arg569Gly)
7g.55191755C>TCA4266107EGFRc.2506C>T (p.Arg836Cys)
c.*28+18827C>T (n.*28+18827C>T)
c.2371C>T (p.Arg791Cys)
c.2347C>T (p.Arg783Cys)
c.1705C>T (p.Arg569Cys)
ClinVar dbSNP ExAC gnomAD COSMIC
7g.55191756G>ACA4266108EGFRc.2507G>A (p.Arg836His)
c.*28+18828G>A (n.*28+18828G>A)
c.2372G>A (p.Arg791His)
c.2348G>A (p.Arg783His)
c.1706G>A (p.Arg569His)
ClinVar dbSNP ExAC gnomAD COSMIC
7g.55191756G>CCA367580139EGFRc.2507G>C (p.Arg836Pro)
c.*28+18828G>C (n.*28+18828G>C)
c.2372G>C (p.Arg791Pro)
c.2348G>C (p.Arg783Pro)
c.1706G>C (p.Arg569Pro)
7g.55191756G=CA1708922490EGFRc.2507G= (p.Arg836=)
c.*28+18828G= (n.*28+18828G=)
c.2372G= (p.Arg791=)
c.2348G= (p.Arg783=)
c.1706G= (p.Arg569=)
7g.55191756G>TCA367580140EGFRc.2507G>T (p.Arg836Leu)
c.*28+18828G>T (n.*28+18828G>T)
c.2372G>T (p.Arg791Leu)
c.2348G>T (p.Arg783Leu)
c.1706G>T (p.Arg569Leu)
7g.55191757C>ACA454965598EGFRc.2508C>A (p.Arg836=)
c.*28+18829C>A (n.*28+18829C>A)
c.2373C>A (p.Arg791=)
c.2349C>A (p.Arg783=)
c.1707C>A (p.Arg569=)
gnomAD
7g.55191757C=CA1708922501EGFRc.2508C= (p.Arg836=)
c.*28+18829C= (n.*28+18829C=)
c.2373C= (p.Arg791=)
c.2349C= (p.Arg783=)
c.1707C= (p.Arg569=)
7g.55191757C>GCA4266109EGFRc.2508C>G (p.Arg836=)
c.*28+18829C>G (n.*28+18829C>G)
c.2373C>G (p.Arg791=)
c.2349C>G (p.Arg783=)
c.1707C>G (p.Arg569=)
dbSNP ExAC gnomAD
7g.55191757C>TCA135924EGFRc.2508C>T (p.Arg836=)
c.*28+18829C>T (n.*28+18829C>T)
c.2373C>T (p.Arg791=)
c.2349C>T (p.Arg783=)
c.1707C>T (p.Arg569=)
ClinVar dbSNP ExAC gnomAD COSMIC
7g.55191758G>ACA4266110EGFRc.2509G>A (p.Asp837Asn)
c.*28+18830G>A (n.*28+18830G>A)
c.2374G>A (p.Asp792Asn)
c.2350G>A (p.Asp784Asn)
c.1708G>A (p.Asp570Asn)
ClinVar dbSNP ExAC gnomAD
7g.55191758G>CCA367580142EGFRc.2509G>C (p.Asp837His)
c.*28+18830G>C (n.*28+18830G>C)
c.2374G>C (p.Asp792His)
c.2350G>C (p.Asp784His)
c.1708G>C (p.Asp570His)
7g.55191758G=CA1708922508EGFRc.2509G= (p.Asp837=)
c.*28+18830G= (n.*28+18830G=)
c.2374G= (p.Asp792=)
c.2350G= (p.Asp784=)
c.1708G= (p.Asp570=)
7g.55191758G>TCA367580141EGFRc.2509G>T (p.Asp837Tyr)
c.*28+18830G>T (n.*28+18830G>T)
c.2374G>T (p.Asp792Tyr)
c.2350G>T (p.Asp784Tyr)
c.1708G>T (p.Asp570Tyr)
7g.55191759A=CA1708922512EGFRc.2510A= (p.Asp837=)
c.*28+18831A= (n.*28+18831A=)
c.2375A= (p.Asp792=)
c.2351A= (p.Asp784=)
c.1709A= (p.Asp570=)

Number of alleles fetched