Chr Mutation (hg38) CAid Gene Transcript Linkouts
7g.55174766_55174786delinsTATCAAGGAATTAAGAGAAGCCA1708918302EGFRc.2070_2090delinsTATCAAGGAATTAAGAGAAGC (p.Ala690=)
c.578_598delinsTATCAAGGAATTAAGAGAAGC
c.2229_2249delinsTATCAAGGAATTAAGAGAAGC (p.Ala743=)
c.*28+1838_*28+1858delinsTATCAAGGAATTAAGAGAAGC (n.*28+1838_*28+1858delinsTATCAAGGAATTAAGAGAAGC)
c.2094_2114delinsTATCAAGGAATTAAGAGAAGC (p.Ala698=)
c.1428_1448delinsTATCAAGGAATTAAGAGAAGC (p.Ala476=)
7g.55174766_55174789delinsAATTAAGACA645561481EGFRc.2070_2093delinsAATTAAGA (p.Glu693AsnfsTer15)
c.578_601delinsAATTAAGA
c.2229_2252delinsAATTAAGA (p.Glu746AsnfsTer15)
c.*28+1838_*28+1861delinsAATTAAGA (n.*28+1838_*28+1861delinsAATTAAGA)
c.2094_2117delinsAATTAAGA (p.Glu701AsnfsTer15)
c.1428_1451delinsAATTAAGA (p.Glu479AsnfsTer15)
COSMIC
7g.55174767_55174786delinsGTCAACA175993EGFRc.2071_2090delinsGTCAA (p.Ile691_Ala697delinsValLys)
c.579_598delinsGTCAA
c.2230_2249delinsGTCAA (p.Ile744_Ala750delinsValLys)
c.*28+1839_*28+1858delinsGTCAA (n.*28+1839_*28+1858delinsGTCAA)
c.2095_2114delinsGTCAA (p.Ile699_Ala705delinsValLys)
c.1429_1448delinsGTCAA (p.Ile477_Ala483delinsValLys)
ClinVar dbSNP COSMIC
7g.55174768_55174786delinsTCAAGGAATTAAGAGAAGCCA1708918305EGFRc.2072_2090delinsTCAAGGAATTAAGAGAAGC (p.Ile691=)
c.580_598delinsTCAAGGAATTAAGAGAAGC
c.2231_2249delinsTCAAGGAATTAAGAGAAGC (p.Ile744=)
c.*28+1840_*28+1858delinsTCAAGGAATTAAGAGAAGC (n.*28+1840_*28+1858delinsTCAAGGAATTAAGAGAAGC)
c.2096_2114delinsTCAAGGAATTAAGAGAAGC (p.Ile699=)
c.1430_1448delinsTCAAGGAATTAAGAGAAGC (p.Ile477=)
7g.55174768_55174787delinsTCAAGGAATTAAGAGAAGCACA1708918306EGFRc.2072_2091delinsTCAAGGAATTAAGAGAAGCA (p.Ile691=)
c.580_599delinsTCAAGGAATTAAGAGAAGCA
c.2231_2250delinsTCAAGGAATTAAGAGAAGCA (p.Ile744=)
c.*28+1840_*28+1859delinsTCAAGGAATTAAGAGAAGCA (n.*28+1840_*28+1859delinsTCAAGGAATTAAGAGAAGCA)
c.2096_2115delinsTCAAGGAATTAAGAGAAGCA (p.Ile699=)
c.1430_1449delinsTCAAGGAATTAAGAGAAGCA (p.Ile477=)
7g.55174768_55174789delinsTCAAGGAATTAAGAGAAGCAACCA1708918308EGFRc.2072_2093delinsTCAAGGAATTAAGAGAAGCAAC (p.Ile691=)
c.580_601delinsTCAAGGAATTAAGAGAAGCAAC
c.2231_2252delinsTCAAGGAATTAAGAGAAGCAAC (p.Ile744=)
c.*28+1840_*28+1861delinsTCAAGGAATTAAGAGAAGCAAC (n.*28+1840_*28+1861delinsTCAAGGAATTAAGAGAAGCAAC)
c.2096_2117delinsTCAAGGAATTAAGAGAAGCAAC (p.Ile699=)
c.1430_1451delinsTCAAGGAATTAAGAGAAGCAAC (p.Ile477=)
7g.55174769_55174786delCA645561484EGFRc.2073_2090del (p.Lys692_Ala697del)
c.581_598del
c.2232_2249del (p.Lys745_Ala750del)
c.*28+1841_*28+1858del (n.*28+1841_*28+1858del)
c.2097_2114del (p.Lys700_Ala705del)
c.1431_1448del (p.Lys478_Ala483del)
dbSNP COSMIC
7g.55174769_55174786delinsAAACA135794EGFRc.2073_2090delinsAAA (p.Glu693_Ala697del)
c.581_598delinsAAA
c.2232_2249delinsAAA (p.Glu746_Ala750del)
c.*28+1841_*28+1858delinsAAA (n.*28+1841_*28+1858delinsAAA)
c.2097_2114delinsAAA (p.Glu701_Ala705del)
c.1431_1448delinsAAA (p.Glu479_Ala483del)
ClinVar dbSNP COSMIC
7g.55174769_55174787delCA180767EGFRc.2073_2091del (p.Lys692HisfsTer15)
c.581_599del
c.2232_2250del (p.Lys745HisfsTer15)
c.*28+1841_*28+1859del (n.*28+1841_*28+1859del)
c.2097_2115del (p.Lys700HisfsTer15)
c.1431_1449del (p.Lys478HisfsTer15)
ClinVar dbSNP
7g.55174769_55174789delinsAAAGTTCA181093EGFRc.2073_2093delinsAAAGTT (p.Glu693_Thr698delinsLeu)
c.581_601delinsAAAGTT
c.2232_2252delinsAAAGTT (p.Glu746_Thr751delinsLeu)
c.*28+1841_*28+1861delinsAAAGTT (n.*28+1841_*28+1861delinsAAAGTT)
c.2097_2117delinsAAAGTT (p.Glu701_Thr706delinsLeu)
c.1431_1451delinsAAAGTT (p.Glu479_Thr484delinsLeu)
ClinVar dbSNP
7g.55174771_55174785delCA645561486EGFRc.2075_2089del (p.Lys692_Ala697delinsThr)
c.583_597del
c.2234_2248del (p.Lys745_Ala750delinsThr)
c.*28+1843_*28+1857del (n.*28+1843_*28+1857del)
c.2099_2113del (p.Lys700_Ala705delinsThr)
c.1433_1447del (p.Lys478_Ala483delinsThr)
dbSNP COSMIC
7g.55174771_55174785delinsAGGAATTAAGAGAAGCA1708918314EGFRc.2075_2089delinsAGGAATTAAGAGAAG (p.Lys692=)
c.583_597delinsAGGAATTAAGAGAAG
c.2234_2248delinsAGGAATTAAGAGAAG (p.Lys745=)
c.*28+1843_*28+1857delinsAGGAATTAAGAGAAG (n.*28+1843_*28+1857delinsAGGAATTAAGAGAAG)
c.2099_2113delinsAGGAATTAAGAGAAG (p.Lys700=)
c.1433_1447delinsAGGAATTAAGAGAAG (p.Lys478=)
7g.55174771_55174786delinsAGGAATTAAGAGAAGCCA1708918311EGFRc.2075_2090delinsAGGAATTAAGAGAAGC (p.Lys692=)
c.583_598delinsAGGAATTAAGAGAAGC
c.2234_2249delinsAGGAATTAAGAGAAGC (p.Lys745=)
c.*28+1843_*28+1858delinsAGGAATTAAGAGAAGC (n.*28+1843_*28+1858delinsAGGAATTAAGAGAAGC)
c.2099_2114delinsAGGAATTAAGAGAAGC (p.Lys700=)
c.1433_1448delinsAGGAATTAAGAGAAGC (p.Lys478=)
7g.55174771_55174788delinsAGGAATTAAGAGAAGCAACA1708918315EGFRc.2075_2092delinsAGGAATTAAGAGAAGCAA (p.Lys692=)
c.583_600delinsAGGAATTAAGAGAAGCAA
c.2234_2251delinsAGGAATTAAGAGAAGCAA (p.Lys745=)
c.*28+1843_*28+1860delinsAGGAATTAAGAGAAGCAA (n.*28+1843_*28+1860delinsAGGAATTAAGAGAAGCAA)
c.2099_2116delinsAGGAATTAAGAGAAGCAA (p.Lys700=)
c.1433_1450delinsAGGAATTAAGAGAAGCAA (p.Lys478=)
7g.55174772_55174785delinsAATTCCA180619EGFRc.2076_2089delinsAATTC (p.Glu693_Ala697delinsIlePro)
c.584_597delinsAATTC
c.2235_2248delinsAATTC (p.Glu746_Ala750delinsIlePro)
c.*28+1844_*28+1857delinsAATTC (n.*28+1844_*28+1857delinsAATTC)
c.2100_2113delinsAATTC (p.Glu701_Ala705delinsIlePro)
c.1434_1447delinsAATTC (p.Glu479_Ala483delinsIlePro)
ClinVar dbSNP COSMIC
7g.55174772_55174786delCA175996EGFRc.2076_2090del (p.Glu693_Ala697del)
c.584_598del
c.2235_2249del (p.Glu746_Ala750del)
c.*28+1844_*28+1858del (n.*28+1844_*28+1858del)
c.2100_2114del (p.Glu701_Ala705del)
c.1434_1448del (p.Glu479_Ala483del)
ClinVar dbSNP COSMIC
7g.55174772_55174787delinsGGAATTAAGAGAAGCACA1708918317EGFRc.2076_2091delinsGGAATTAAGAGAAGCA (p.Lys692=)
c.584_599delinsGGAATTAAGAGAAGCA
c.2235_2250delinsGGAATTAAGAGAAGCA (p.Lys745=)
c.*28+1844_*28+1859delinsGGAATTAAGAGAAGCA (n.*28+1844_*28+1859delinsGGAATTAAGAGAAGCA)
c.2100_2115delinsGGAATTAAGAGAAGCA (p.Lys700=)
c.1434_1449delinsGGAATTAAGAGAAGCA (p.Lys478=)
7g.55174772_55174788delinsAGCA645561492EGFRc.2076_2092delinsAG (p.Glu693_Thr698delinsAla)
c.584_600delinsAG
c.2235_2251delinsAG (p.Glu746_Thr751delinsAla)
c.*28+1844_*28+1860delinsAG (n.*28+1844_*28+1860delinsAG)
c.2100_2116delinsAG (p.Glu701_Thr706delinsAla)
c.1434_1450delinsAG (p.Glu479_Thr484delinsAla)
dbSNP COSMIC
7g.55174772_55174788delinsAATTCCA180803EGFRc.2076_2092delinsAATTC (p.Glu693_Thr698delinsIlePro)
c.584_600delinsAATTC
c.2235_2251delinsAATTC (p.Glu746_Thr751delinsIlePro)
c.*28+1844_*28+1860delinsAATTC (n.*28+1844_*28+1860delinsAATTC)
c.2100_2116delinsAATTC (p.Glu701_Thr706delinsIlePro)
c.1434_1450delinsAATTC (p.Glu479_Thr484delinsIlePro)
ClinVar dbSNP COSMIC
7g.55174772_55174789delCA645561489EGFRc.2076_2093del (p.Glu693_Thr698del)
c.584_601del
c.2235_2252del (p.Glu746_Thr751del)
c.*28+1844_*28+1861del (n.*28+1844_*28+1861del)
c.2100_2117del (p.Glu701_Thr706del)
c.1434_1451del (p.Glu479_Thr484del)
dbSNP COSMIC
7g.55174772_55174789delinsAATCA645561490EGFRc.2076_2093delinsAAT (p.Glu693_Thr698delinsIle)
c.584_601delinsAAT
c.2235_2252delinsAAT (p.Glu746_Thr751delinsIle)
c.*28+1844_*28+1861delinsAAT (n.*28+1844_*28+1861delinsAAT)
c.2100_2117delinsAAT (p.Glu701_Thr706delinsIle)
c.1434_1451delinsAAT (p.Glu479_Thr484delinsIle)
dbSNP COSMIC
7g.55174772_55174789delinsGGAATTAAGAGAAGCAACCA1708918316EGFRc.2076_2093delinsGGAATTAAGAGAAGCAAC (p.Lys692=)
c.584_601delinsGGAATTAAGAGAAGCAAC
c.2235_2252delinsGGAATTAAGAGAAGCAAC (p.Lys745=)
c.*28+1844_*28+1861delinsGGAATTAAGAGAAGCAAC (n.*28+1844_*28+1861delinsGGAATTAAGAGAAGCAAC)
c.2100_2117delinsGGAATTAAGAGAAGCAAC (p.Lys700=)
c.1434_1451delinsGGAATTAAGAGAAGCAAC (p.Lys478=)
7g.55174772_55174790delinsGGAATTAAGAGAAGCAACACA1708918319EGFRc.2076_2094delinsGGAATTAAGAGAAGCAACA (p.Lys692=)
c.584_602delinsGGAATTAAGAGAAGCAACA
c.2235_2253delinsGGAATTAAGAGAAGCAACA (p.Lys745=)
c.*28+1844_*28+1862delinsGGAATTAAGAGAAGCAACA (n.*28+1844_*28+1862delinsGGAATTAAGAGAAGCAACA)
c.2100_2118delinsGGAATTAAGAGAAGCAACA (p.Lys700=)
c.1434_1452delinsGGAATTAAGAGAAGCAACA (p.Lys478=)
7g.55174772_55174792delinsAATCA645561491EGFRc.2076_2096delinsAAT (p.Glu693_Ser699delinsIle)
c.584_604delinsAAT
c.2235_2255delinsAAT (p.Glu746_Ser752delinsIle)
c.*28+1844_*28+1864delinsAAT (n.*28+1844_*28+1864delinsAAT)
c.2100_2120delinsAAT (p.Glu701_Ser707delinsIle)
c.1434_1454delinsAAT (p.Glu479_Ser485delinsIle)
dbSNP COSMIC
7g.55174772_55174792delinsAGTCA2573049007EGFRc.2076_2096delinsAGT (p.Glu693_Ser699delinsVal)
c.584_604delinsAGT
c.2235_2255delinsAGT (p.Glu746_Ser752delinsVal)
c.*28+1844_*28+1864delinsAGT (n.*28+1844_*28+1864delinsAGT)
c.2100_2120delinsAGT (p.Glu701_Ser707delinsVal)
c.1434_1454delinsAGT (p.Glu479_Ser485delinsVal)
7g.55174773_55174785delinsAGACCA645561499EGFRc.2077_2089delinsAGAC (p.Glu693_Ala697delinsArgPro)
c.585_597delinsAGAC
c.2236_2248delinsAGAC (p.Glu746_Ala750delinsArgPro)
c.*28+1845_*28+1857delinsAGAC (n.*28+1845_*28+1857delinsAGAC)
c.2101_2113delinsAGAC (p.Glu701_Ala705delinsArgPro)
c.1435_1447delinsAGAC (p.Glu479_Ala483delinsArgPro)
dbSNP COSMIC
7g.55174773_55174785delinsCAACCA645561497EGFRc.2077_2089delinsCAAC (p.Glu693_Ala697delinsGlnPro)
c.585_597delinsCAAC
c.2236_2248delinsCAAC (p.Glu746_Ala750delinsGlnPro)
c.*28+1845_*28+1857delinsCAAC (n.*28+1845_*28+1857delinsCAAC)
c.2101_2113delinsCAAC (p.Glu701_Ala705delinsGlnPro)
c.1435_1447delinsCAAC (p.Glu479_Ala483delinsGlnPro)
dbSNP COSMIC
7g.55174773_55174785delinsGAATTAAGAGAAGCA1708918324EGFRc.2077_2089delinsGAATTAAGAGAAG (p.Glu693=)
c.585_597delinsGAATTAAGAGAAG
c.2236_2248delinsGAATTAAGAGAAG (p.Glu746=)
c.*28+1845_*28+1857delinsGAATTAAGAGAAG (n.*28+1845_*28+1857delinsGAATTAAGAGAAG)
c.2101_2113delinsGAATTAAGAGAAG (p.Glu701=)
c.1435_1447delinsGAATTAAGAGAAG (p.Glu479=)
7g.55174774_55174785delCA891842001EGFRc.2078_2089del (p.Glu693_Glu696del)
c.586_597del
c.2237_2248del (p.Glu746_Glu749del)
c.*28+1846_*28+1857del (n.*28+1846_*28+1857del)
c.2102_2113del (p.Glu701_Glu704del)
c.1436_1447del (p.Glu479_Glu482del)
7g.55174773_55174787delCA180531EGFRc.2077_2091del (p.Glu693_Ala697del)
c.585_599del
c.2236_2250del (p.Glu746_Ala750del)
c.*28+1845_*28+1859del (n.*28+1845_*28+1859del)
c.2101_2115del (p.Glu701_Ala705del)
c.1435_1449del (p.Glu479_Ala483del)
ClinVar dbSNP COSMIC
7g.55174773_55174788delinsTCA645561502EGFRc.2077_2092delinsT (p.Glu693_Thr698delinsSer)
c.585_600delinsT
c.2236_2251delinsT (p.Glu746_Thr751delinsSer)
c.*28+1845_*28+1860delinsT (n.*28+1845_*28+1860delinsT)
c.2101_2116delinsT (p.Glu701_Thr706delinsSer)
c.1435_1450delinsT (p.Glu479_Thr484delinsSer)
dbSNP COSMIC
7g.55174773_55174788delinsGAATTAAGAGAAGCAACA1708918323EGFRc.2077_2092delinsGAATTAAGAGAAGCAA (p.Glu693=)
c.585_600delinsGAATTAAGAGAAGCAA
c.2236_2251delinsGAATTAAGAGAAGCAA (p.Glu746=)
c.*28+1845_*28+1860delinsGAATTAAGAGAAGCAA (n.*28+1845_*28+1860delinsGAATTAAGAGAAGCAA)
c.2101_2116delinsGAATTAAGAGAAGCAA (p.Glu701=)
c.1435_1450delinsGAATTAAGAGAAGCAA (p.Glu479=)
7g.55174773_55174789delinsATCA181002EGFRc.2077_2093delinsAT (p.Glu693_Thr698delinsIle)
c.585_601delinsAT
c.2236_2252delinsAT (p.Glu746_Thr751delinsIle)
c.*28+1845_*28+1861delinsAT (n.*28+1845_*28+1861delinsAT)
c.2101_2117delinsAT (p.Glu701_Thr706delinsIle)
c.1435_1451delinsAT (p.Glu479_Thr484delinsIle)
ClinVar dbSNP COSMIC
7g.55174773_55174789delinsCACA645561494EGFRc.2077_2093delinsCA (p.Glu693_Thr698delinsGln)
c.585_601delinsCA
c.2236_2252delinsCA (p.Glu746_Thr751delinsGln)
c.*28+1845_*28+1861delinsCA (n.*28+1845_*28+1861delinsCA)
c.2101_2117delinsCA (p.Glu701_Thr706delinsGln)
c.1435_1451delinsCA (p.Glu479_Thr484delinsGln)
dbSNP COSMIC
7g.55174773_55174789delinsCTCA645561500EGFRc.2077_2093delinsCT (p.Glu693_Thr698delinsLeu)
c.585_601delinsCT
c.2236_2252delinsCT (p.Glu746_Thr751delinsLeu)
c.*28+1845_*28+1861delinsCT (n.*28+1845_*28+1861delinsCT)
c.2101_2117delinsCT (p.Glu701_Thr706delinsLeu)
c.1435_1451delinsCT (p.Glu479_Thr484delinsLeu)
dbSNP COSMIC COSMIC
7g.55174773_55174790delCA158932568EGFRc.2077_2094del (p.Glu693_Thr698del)
c.585_602del
c.2236_2253del (p.Glu746_Thr751del)
c.*28+1845_*28+1862del (n.*28+1845_*28+1862del)
c.2101_2118del (p.Glu701_Thr706del)
c.1435_1452del (p.Glu479_Thr484del)
dbSNP COSMIC
7g.55174773_55174790delinsATGCA2714959368EGFRc.2077_2094delinsATG (p.Glu693_Thr698delinsMet)
c.585_602delinsATG
c.2236_2253delinsATG (p.Glu746_Thr751delinsMet)
c.*28+1845_*28+1862delinsATG (n.*28+1845_*28+1862delinsATG)
c.2101_2118delinsATG (p.Glu701_Thr706delinsMet)
c.1435_1452delinsATG (p.Glu479_Thr484delinsMet)
dbSNP
7g.55174773_55174790delinsATTCCTCA645561498EGFRc.2077_2094delinsATTCCT (p.Glu693_Thr698delinsIlePro)
c.585_602delinsATTCCT
c.2236_2253delinsATTCCT (p.Glu746_Thr751delinsIlePro)
c.*28+1845_*28+1862delinsATTCCT (n.*28+1845_*28+1862delinsATTCCT)
c.2101_2118delinsATTCCT (p.Glu701_Thr706delinsIlePro)
c.1435_1452delinsATTCCT (p.Glu479_Thr484delinsIlePro)
dbSNP COSMIC
7g.55174773_55174791delinsGAATTAAGAGAAGCAACATCA1708918327EGFRc.2077_2095delinsGAATTAAGAGAAGCAACAT (p.Glu693=)
c.585_603delinsGAATTAAGAGAAGCAACAT
c.2236_2254delinsGAATTAAGAGAAGCAACAT (p.Glu746=)
c.*28+1845_*28+1863delinsGAATTAAGAGAAGCAACAT (n.*28+1845_*28+1863delinsGAATTAAGAGAAGCAACAT)
c.2101_2119delinsGAATTAAGAGAAGCAACAT (p.Glu701=)
c.1435_1453delinsGAATTAAGAGAAGCAACAT (p.Glu479=)
7g.55174773_55174792delinsATCA645561495EGFRc.2077_2096delinsAT (p.Glu693_Ser699delinsIle)
c.585_604delinsAT
c.2236_2255delinsAT (p.Glu746_Ser752delinsIle)
c.*28+1845_*28+1864delinsAT (n.*28+1845_*28+1864delinsAT)
c.2101_2120delinsAT (p.Glu701_Ser707delinsIle)
c.1435_1454delinsAT (p.Glu479_Ser485delinsIle)
dbSNP COSMIC
7g.55174773_55174792delinsGAATTAAGAGAAGCAACATCCA1708918322EGFRc.2077_2096delinsGAATTAAGAGAAGCAACATC (p.Glu693=)
c.585_604delinsGAATTAAGAGAAGCAACATC
c.2236_2255delinsGAATTAAGAGAAGCAACATC (p.Glu746=)
c.*28+1845_*28+1864delinsGAATTAAGAGAAGCAACATC (n.*28+1845_*28+1864delinsGAATTAAGAGAAGCAACATC)
c.2101_2120delinsGAATTAAGAGAAGCAACATC (p.Glu701=)
c.1435_1454delinsGAATTAAGAGAAGCAACATC (p.Glu479=)
7g.55174773_55174793delCA645561501EGFRc.2077_2097del (p.Glu693_Ser699del)
c.585_605del
c.2236_2256del (p.Glu746_Ser752del)
c.*28+1845_*28+1865del (n.*28+1845_*28+1865del)
c.2101_2121del (p.Glu701_Ser707del)
c.1435_1455del (p.Glu479_Ser485del)
COSMIC
7g.55174773_55174793delinsATCCA645561505EGFRc.2077_2097delinsATC (p.Glu693_Ser699delinsIle)
c.585_605delinsATC
c.2236_2256delinsATC (p.Glu746_Ser752delinsIle)
c.*28+1845_*28+1865delinsATC (n.*28+1845_*28+1865delinsATC)
c.2101_2121delinsATC (p.Glu701_Ser707delinsIle)
c.1435_1455delinsATC (p.Glu479_Ser485delinsIle)
dbSNP COSMIC
7g.55174773_55174793delinsGAATTAAGAGAAGCAACATCTCA1708918326EGFRc.2077_2097delinsGAATTAAGAGAAGCAACATCT (p.Glu693=)
c.585_605delinsGAATTAAGAGAAGCAACATCT
c.2236_2256delinsGAATTAAGAGAAGCAACATCT (p.Glu746=)
c.*28+1845_*28+1865delinsGAATTAAGAGAAGCAACATCT (n.*28+1845_*28+1865delinsGAATTAAGAGAAGCAACATCT)
c.2101_2121delinsGAATTAAGAGAAGCAACATCT (p.Glu701=)
c.1435_1455delinsGAATTAAGAGAAGCAACATCT (p.Glu479=)
7g.55174773_55174794delinsATCTCA645561504EGFRc.2077_2098delinsATCT (p.Glu693_Pro700delinsIleSer)
c.585_606delinsATCT
c.2236_2257delinsATCT (p.Glu746_Pro753delinsIleSer)
c.*28+1845_*28+1866delinsATCT (n.*28+1845_*28+1866delinsATCT)
c.2101_2122delinsATCT (p.Glu701_Pro708delinsIleSer)
c.1435_1456delinsATCT (p.Glu479_Pro486delinsIleSer)
dbSNP COSMIC
7g.55174773_55174794delinsCTCTCA645561496EGFRc.2077_2098delinsCTCT (p.Glu693_Pro700delinsLeuSer)
c.585_606delinsCTCT
c.2236_2257delinsCTCT (p.Glu746_Pro753delinsLeuSer)
c.*28+1845_*28+1866delinsCTCT (n.*28+1845_*28+1866delinsCTCT)
c.2101_2122delinsCTCT (p.Glu701_Pro708delinsLeuSer)
c.1435_1456delinsCTCT (p.Glu479_Pro486delinsLeuSer)
dbSNP COSMIC
7g.55174773_55174794delinsGAATTAAGAGAAGCAACATCTCCA1708918321EGFRc.2077_2098delinsGAATTAAGAGAAGCAACATCTC (p.Glu693=)
c.585_606delinsGAATTAAGAGAAGCAACATCTC
c.2236_2257delinsGAATTAAGAGAAGCAACATCTC (p.Glu746=)
c.*28+1845_*28+1866delinsGAATTAAGAGAAGCAACATCTC (n.*28+1845_*28+1866delinsGAATTAAGAGAAGCAACATCTC)
c.2101_2122delinsGAATTAAGAGAAGCAACATCTC (p.Glu701=)
c.1435_1456delinsGAATTAAGAGAAGCAACATCTC (p.Glu479=)
7g.55174774_55174785delinsCACCA180653EGFRc.2078_2089delinsCAC (p.Glu693_Ala697delinsAlaPro)
c.586_597delinsCAC
c.2237_2248delinsCAC (p.Glu746_Ala750delinsAlaPro)
c.*28+1846_*28+1857delinsCAC (n.*28+1846_*28+1857delinsCAC)
c.2102_2113delinsCAC (p.Glu701_Ala705delinsAlaPro)
c.1436_1447delinsCAC (p.Glu479_Ala483delinsAlaPro)
ClinVar dbSNP COSMIC
7g.55174774_55174785delinsCCCCA175997EGFRc.2078_2089delinsCCC (p.Glu693_Ala697delinsAlaPro)
c.586_597delinsCCC
c.2237_2248delinsCCC (p.Glu746_Ala750delinsAlaPro)
c.*28+1846_*28+1857delinsCCC (n.*28+1846_*28+1857delinsCCC)
c.2102_2113delinsCCC (p.Glu701_Ala705delinsAlaPro)
c.1436_1447delinsCCC (p.Glu479_Ala483delinsAlaPro)
ClinVar dbSNP
7g.55174774_55174785delinsAATTAAGAGAAGCA1708918330EGFRc.2078_2089delinsAATTAAGAGAAG (p.Glu693=)
c.586_597delinsAATTAAGAGAAG
c.2237_2248delinsAATTAAGAGAAG (p.Glu746=)
c.*28+1846_*28+1857delinsAATTAAGAGAAG (n.*28+1846_*28+1857delinsAATTAAGAGAAG)
c.2102_2113delinsAATTAAGAGAAG (p.Glu701=)
c.1436_1447delinsAATTAAGAGAAG (p.Glu479=)

Number of alleles fetched