Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
7 | g.55174766_55174786delinsTATCAAGGAATTAAGAGAAGC | CA1708918302 | EGFR | c.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=) | |
7 | g.55174766_55174789delinsAATTAAGA | CA645561481 | EGFR | c.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 |
7 | g.55174767_55174783delinsCTTAAGAG | CA645561483 | EGFR | c.2071_2087delinsCTTAAGAG (p.Ile691_Glu696delinsLeuLysArg) c.579_595delinsCTTAAGAG c.2230_2246delinsCTTAAGAG (p.Ile744_Glu749delinsLeuLysArg) c.*28+1839_*28+1855delinsCTTAAGAG (n.*28+1839_*28+1855delinsCTTAAGAG) c.2095_2111delinsCTTAAGAG (p.Ile699_Glu704delinsLeuLysArg) c.1429_1445delinsCTTAAGAG (p.Ile477_Glu482delinsLeuLysArg) | dbSNP COSMIC |
7 | g.55174767_55174786delinsGTCAA | CA175993 | EGFR | c.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 |
7 | g.55174768_55174786delinsTCAAGGAATTAAGAGAAGC | CA1708918305 | EGFR | c.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=) | |
7 | g.55174768_55174787delinsTCAAGGAATTAAGAGAAGCA | CA1708918306 | EGFR | c.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=) | |
7 | g.55174768_55174789delinsTCAAGGAATTAAGAGAAGCAAC | CA1708918308 | EGFR | c.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=) | |
7 | g.55174769_55174786del | CA645561484 | EGFR | c.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 |
7 | g.55174769_55174786delinsAAA | CA135794 | EGFR | c.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 |
7 | g.55174769_55174787del | CA180767 | EGFR | c.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 |
7 | g.55174769_55174789delinsAAAGTT | CA181093 | EGFR | c.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 |
7 | g.55174770_55174784del | CA645561485 | EGFR | c.2074_2088del (p.Lys692_Glu696del) c.582_596del c.2233_2247del (p.Lys745_Glu749del) c.*28+1842_*28+1856del (n.*28+1842_*28+1856del) c.2098_2112del (p.Lys700_Glu704del) c.1432_1446del (p.Lys478_Glu482del) | dbSNP COSMIC |
7 | g.55174771_55174780delinsAGGAATTAAG | CA1708918313 | EGFR | c.2075_2084delinsAGGAATTAAG (p.Lys692=) c.583_592delinsAGGAATTAAG c.2234_2243delinsAGGAATTAAG (p.Lys745=) c.*28+1843_*28+1852delinsAGGAATTAAG (n.*28+1843_*28+1852delinsAGGAATTAAG) c.2099_2108delinsAGGAATTAAG (p.Lys700=) c.1433_1442delinsAGGAATTAAG (p.Lys478=) | |
7 | g.55174772_55174783del | CA645561487 | EGFR | c.2076_2087del (p.Glu693_Glu696del) c.584_595del c.2235_2246del (p.Glu746_Glu749del) c.*28+1844_*28+1855del (n.*28+1844_*28+1855del) c.2100_2111del (p.Glu701_Glu704del) c.1434_1445del (p.Glu479_Glu482del) | dbSNP COSMIC |
7 | g.55174771_55174785del | CA645561486 | EGFR | c.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 |
7 | g.55174771_55174785delinsAGGAATTAAGAGAAG | CA1708918314 | EGFR | c.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=) | |
7 | g.55174771_55174786delinsAGGAATTAAGAGAAGC | CA1708918311 | EGFR | c.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=) | |
7 | g.55174771_55174788delinsAGGAATTAAGAGAAGCAA | CA1708918315 | EGFR | c.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=) | |
7 | g.55174772_55174780del | CA180594 | EGFR | c.2076_2084del (p.Glu693_Arg695del) c.584_592del c.2235_2243del (p.Glu746_Arg748del) c.*28+1844_*28+1852del (n.*28+1844_*28+1852del) c.2100_2108del (p.Glu701_Arg703del) c.1434_1442del (p.Glu479_Arg481del) | ClinVar dbSNP |
7 | g.55174772_55174781delinsGGAATTAAGA | CA1708918318 | EGFR | c.2076_2085delinsGGAATTAAGA (p.Lys692=) c.584_593delinsGGAATTAAGA c.2235_2244delinsGGAATTAAGA (p.Lys745=) c.*28+1844_*28+1853delinsGGAATTAAGA (n.*28+1844_*28+1853delinsGGAATTAAGA) c.2100_2109delinsGGAATTAAGA (p.Lys700=) c.1434_1443delinsGGAATTAAGA (p.Lys478=) | |
7 | g.55174772_55174785delinsAATTC | CA180619 | EGFR | c.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 |
7 | g.55174772_55174786del | CA175996 | EGFR | c.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 |
7 | g.55174772_55174787delinsGGAATTAAGAGAAGCA | CA1708918317 | EGFR | c.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=) | |
7 | g.55174772_55174788delinsAG | CA645561492 | EGFR | c.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 |
7 | g.55174772_55174788delinsAATTC | CA180803 | EGFR | c.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 |
7 | g.55174772_55174789del | CA645561489 | EGFR | c.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 |
7 | g.55174772_55174789delinsAAT | CA645561490 | EGFR | c.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 |
7 | g.55174772_55174789delinsGGAATTAAGAGAAGCAAC | CA1708918316 | EGFR | c.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=) | |
7 | g.55174772_55174790delinsGGAATTAAGAGAAGCAACA | CA1708918319 | EGFR | c.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=) | |
7 | g.55174772_55174792delinsAAT | CA645561491 | EGFR | c.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 |
7 | g.55174772_55174792delinsAGT | CA2573049007 | EGFR | c.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) | |
7 | g.55174773_55174778delinsAATTAT | CA645561503 | EGFR | c.2077_2082delinsAATTAT (p.Glu693_Leu694delinsAsnTyr) c.585_590delinsAATTAT c.2236_2241delinsAATTAT (p.Glu746_Leu747delinsAsnTyr) c.*28+1845_*28+1850delinsAATTAT (n.*28+1845_*28+1850delinsAATTAT) c.2101_2106delinsAATTAT (p.Glu701_Leu702delinsAsnTyr) c.1435_1440delinsAATTAT (p.Glu479_Leu480delinsAsnTyr) | COSMIC |
7 | g.55174773_55174783delinsGAATTAAGAGA | CA1708918320 | EGFR | c.2077_2087delinsGAATTAAGAGA (p.Glu693=) c.585_595delinsGAATTAAGAGA c.2236_2246delinsGAATTAAGAGA (p.Glu746=) c.*28+1845_*28+1855delinsGAATTAAGAGA (n.*28+1845_*28+1855delinsGAATTAAGAGA) c.2101_2111delinsGAATTAAGAGA (p.Glu701=) c.1435_1445delinsGAATTAAGAGA (p.Glu479=) | |
7 | g.55174776_55174784del | CA180726 | EGFR | c.2080_2088del (p.Leu694_Glu696del) c.588_596del c.2239_2247del (p.Leu747_Glu749del) c.*28+1848_*28+1856del (n.*28+1848_*28+1856del) c.2104_2112del (p.Leu702_Glu704del) c.1438_1446del (p.Leu480_Glu482del) | ClinVar dbSNP COSMIC |
7 | g.55174773_55174785delinsAGAC | CA645561499 | EGFR | c.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 |
7 | g.55174773_55174785delinsCAAC | CA645561497 | EGFR | c.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 |
7 | g.55174773_55174785delinsGAATTAAGAGAAG | CA1708918324 | EGFR | c.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=) | |
7 | g.55174774_55174785del | CA891842001 | EGFR | c.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) | |
7 | g.55174773_55174787del | CA180531 | EGFR | c.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 |
7 | g.55174773_55174788delinsT | CA645561502 | EGFR | c.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 |
7 | g.55174773_55174788delinsGAATTAAGAGAAGCAA | CA1708918323 | EGFR | c.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=) | |
7 | g.55174773_55174789delinsAT | CA181002 | EGFR | c.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 |
7 | g.55174773_55174789delinsCA | CA645561494 | EGFR | c.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 |
7 | g.55174773_55174789delinsCT | CA645561500 | EGFR | c.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 |
7 | g.55174773_55174790del | CA158932568 | EGFR | c.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 |
7 | g.55174773_55174790delinsATG | CA2714959368 | EGFR | c.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 |
7 | g.55174773_55174790delinsATTCCT | CA645561498 | EGFR | c.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 |
7 | g.55174773_55174791delinsGAATTAAGAGAAGCAACAT | CA1708918327 | EGFR | c.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=) | |
7 | g.55174773_55174792delinsAT | CA645561495 | EGFR | c.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 |
7 | g.55174773_55174792delinsGAATTAAGAGAAGCAACATC | CA1708918322 | EGFR | c.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=) | |
7 | g.55174773_55174793del | CA645561501 | EGFR | c.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 |
7 | g.55174773_55174793delinsATC | CA645561505 | EGFR | c.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 |
7 | g.55174773_55174793delinsGAATTAAGAGAAGCAACATCT | CA1708918326 | EGFR | c.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=) | |
7 | g.55174773_55174794delinsATCT | CA645561504 | EGFR | c.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 |
7 | g.55174773_55174794delinsCTCT | CA645561496 | EGFR | c.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 |
7 | g.55174773_55174794delinsGAATTAAGAGAAGCAACATCTC | CA1708918321 | EGFR | c.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=) | |
7 | g.55174774_55174775delinsTT | CA645561511 | EGFR | c.2078_2079delinsTT (p.Glu693Val) c.586_587delinsTT c.2237_2238delinsTT (p.Glu746Val) c.*28+1846_*28+1847delinsTT (n.*28+1846_*28+1847delinsTT) c.2102_2103delinsTT (p.Glu701Val) c.1436_1437delinsTT (p.Glu479Val) | COSMIC |
7 | g.55174775dup | CA2682854897 | EGFR | c.2079dup (p.Leu694IlefsTer16) c.587dup c.2238dup (p.Leu747IlefsTer16) c.*28+1847dup (n.*28+1847dup) c.2103dup (p.Leu702IlefsTer16) c.1437dup (p.Leu480IlefsTer16) | gnomAD v4 |
7 | g.55174774_55174783delinsC | CA182031 | EGFR | c.2078_2087delinsC (p.Glu693_Glu696delinsAla) c.586_595delinsC c.2237_2246delinsC (p.Glu746_Glu749delinsAla) c.*28+1846_*28+1855delinsC (n.*28+1846_*28+1855delinsC) c.2102_2111delinsC (p.Glu701_Glu704delinsAla) c.1436_1445delinsC (p.Glu479_Glu482delinsAla) | ClinVar dbSNP |
7 | g.55174775_55174784del | CA891842011 | EGFR | c.2079_2088del (p.Leu694GlnfsTer16) c.587_596del c.2238_2247del (p.Leu747GlnfsTer16) c.*28+1847_*28+1856del (n.*28+1847_*28+1856del) c.2103_2112del (p.Leu702GlnfsTer16) c.1437_1446del (p.Leu480GlnfsTer16) | |
7 | g.55174774_55174785delinsCAC | CA180653 | EGFR | c.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 |
7 | g.55174774_55174785delinsCCC | CA175997 | EGFR | c.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 |
7 | g.55174774_55174785delinsAATTAAGAGAAG | CA1708918330 | EGFR | c.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=) | |
7 | g.55174774_55174787delinsTCCCT | CA645561513 | EGFR | c.2078_2091delinsTCCCT (p.Glu693_Ala697delinsValPro) c.586_599delinsTCCCT c.2237_2250delinsTCCCT (p.Glu746_Ala750delinsValPro) c.*28+1846_*28+1859delinsTCCCT (n.*28+1846_*28+1859delinsTCCCT) c.2102_2115delinsTCCCT (p.Glu701_Ala705delinsValPro) c.1436_1449delinsTCCCT (p.Glu479_Ala483delinsValPro) | dbSNP COSMIC |
7 | g.55174774_55174788del | CA180560 | EGFR | c.2078_2092del (p.Glu693_Thr698delinsAla) c.586_600del c.2237_2251del (p.Glu746_Thr751delinsAla) c.*28+1846_*28+1860del (n.*28+1846_*28+1860del) c.2102_2116del (p.Glu701_Thr706delinsAla) c.1436_1450del (p.Glu479_Thr484delinsAla) | ClinVar dbSNP COSMIC |
7 | g.55174774_55174788delinsTGG | CA645561508 | EGFR | c.2078_2092delinsTGG (p.Glu693_Thr698delinsValAla) c.586_600delinsTGG c.2237_2251delinsTGG (p.Glu746_Thr751delinsValAla) c.*28+1846_*28+1860delinsTGG (n.*28+1846_*28+1860delinsTGG) c.2102_2116delinsTGG (p.Glu701_Thr706delinsValAla) c.1436_1450delinsTGG (p.Glu479_Thr484delinsValAla) | dbSNP COSMIC |
7 | g.55174774_55174788delinsTTC | CA176000 | EGFR | c.2078_2092delinsTTC (p.Glu693_Thr698delinsValPro) c.586_600delinsTTC c.2237_2251delinsTTC (p.Glu746_Thr751delinsValPro) c.*28+1846_*28+1860delinsTTC (n.*28+1846_*28+1860delinsTTC) c.2102_2116delinsTTC (p.Glu701_Thr706delinsValPro) c.1436_1450delinsTTC (p.Glu479_Thr484delinsValPro) | ClinVar dbSNP COSMIC |
7 | g.55174774_55174788delinsTTG | CA2499306878 | EGFR | c.2078_2092delinsTTG (p.Glu693_Thr698delinsValAla) c.586_600delinsTTG c.2237_2251delinsTTG (p.Glu746_Thr751delinsValAla) c.*28+1846_*28+1860delinsTTG (n.*28+1846_*28+1860delinsTTG) c.2102_2116delinsTTG (p.Glu701_Thr706delinsValAla) c.1436_1450delinsTTG (p.Glu479_Thr484delinsValAla) | |
7 | g.55174774_55174788delinsAATTAAGAGAAGCAA | CA1708918328 | EGFR | c.2078_2092delinsAATTAAGAGAAGCAA (p.Glu693=) c.586_600delinsAATTAAGAGAAGCAA c.2237_2251delinsAATTAAGAGAAGCAA (p.Glu746=) c.*28+1846_*28+1860delinsAATTAAGAGAAGCAA (n.*28+1846_*28+1860delinsAATTAAGAGAAGCAA) c.2102_2116delinsAATTAAGAGAAGCAA (p.Glu701=) c.1436_1450delinsAATTAAGAGAAGCAA (p.Glu479=) | |
7 | g.55174776_55174788del | CA891842010 | EGFR | c.2080_2092del (p.Leu694HisfsTer15) c.588_600del c.2239_2251del (p.Leu747HisfsTer15) c.*28+1848_*28+1860del (n.*28+1848_*28+1860del) c.2104_2116del (p.Leu702HisfsTer15) c.1438_1450del (p.Leu480HisfsTer15) | |
7 | g.55174774_55174789delinsT | CA645561512 | EGFR | c.2078_2093delinsT (p.Glu693_Thr698delinsVal) c.586_601delinsT c.2237_2252delinsT (p.Glu746_Thr751delinsVal) c.*28+1846_*28+1861delinsT (n.*28+1846_*28+1861delinsT) c.2102_2117delinsT (p.Glu701_Thr706delinsVal) c.1436_1451delinsT (p.Glu479_Thr484delinsVal) | dbSNP COSMIC COSMIC |
7 | g.55174774_55174789delinsAATTAAGAGAAGCAAC | CA1708918329 | EGFR | c.2078_2093delinsAATTAAGAGAAGCAAC (p.Glu693=) c.586_601delinsAATTAAGAGAAGCAAC c.2237_2252delinsAATTAAGAGAAGCAAC (p.Glu746=) c.*28+1846_*28+1861delinsAATTAAGAGAAGCAAC (n.*28+1846_*28+1861delinsAATTAAGAGAAGCAAC) c.2102_2117delinsAATTAAGAGAAGCAAC (p.Glu701=) c.1436_1451delinsAATTAAGAGAAGCAAC (p.Glu479=) | |
7 | g.55174774_55174790delinsTC | CA645561507 | EGFR | c.2078_2094delinsTC (p.Glu693_Thr698delinsVal) c.586_602delinsTC c.2237_2253delinsTC (p.Glu746_Thr751delinsVal) c.*28+1846_*28+1862delinsTC (n.*28+1846_*28+1862delinsTC) c.2102_2118delinsTC (p.Glu701_Thr706delinsVal) c.1436_1452delinsTC (p.Glu479_Thr484delinsVal) | dbSNP COSMIC |
7 | g.55174774_55174790delinsTTCCT | CA645561514 | EGFR | c.2078_2094delinsTTCCT (p.Glu693_Thr698delinsValPro) c.586_602delinsTTCCT c.2237_2253delinsTTCCT (p.Glu746_Thr751delinsValPro) c.*28+1846_*28+1862delinsTTCCT (n.*28+1846_*28+1862delinsTTCCT) c.2102_2118delinsTTCCT (p.Glu701_Thr706delinsValPro) c.1436_1452delinsTTCCT (p.Glu479_Thr484delinsValPro) | dbSNP COSMIC |
7 | g.55174774_55174790delinsTTGCT | CA645561515 | EGFR | c.2078_2094delinsTTGCT (p.Glu693_Thr698delinsValAla) c.586_602delinsTTGCT c.2237_2253delinsTTGCT (p.Glu746_Thr751delinsValAla) c.*28+1846_*28+1862delinsTTGCT (n.*28+1846_*28+1862delinsTTGCT) c.2102_2118delinsTTGCT (p.Glu701_Thr706delinsValAla) c.1436_1452delinsTTGCT (p.Glu479_Thr484delinsValAla) | dbSNP COSMIC |
7 | g.55174774_55174791del | CA180654 | EGFR | c.2078_2095del (p.Glu693_Ser699delinsAla) c.586_603del c.2237_2254del (p.Glu746_Ser752delinsAla) c.*28+1846_*28+1863del (n.*28+1846_*28+1863del) c.2102_2119del (p.Glu701_Ser707delinsAla) c.1436_1453del (p.Glu479_Ser485delinsAla) | ClinVar dbSNP COSMIC |
7 | g.55174774_55174792delinsT | CA180574 | EGFR | c.2078_2096delinsT (p.Glu693_Ser699delinsVal) c.586_604delinsT c.2237_2255delinsT (p.Glu746_Ser752delinsVal) c.*28+1846_*28+1864delinsT (n.*28+1846_*28+1864delinsT) c.2102_2120delinsT (p.Glu701_Ser707delinsVal) c.1436_1454delinsT (p.Glu479_Ser485delinsVal) | ClinVar dbSNP COSMIC COSMIC COSMIC |
7 | g.55174774_55174792delinsAATTAAGAGAAGCAACATC | CA1708918331 | EGFR | c.2078_2096delinsAATTAAGAGAAGCAACATC (p.Glu693=) c.586_604delinsAATTAAGAGAAGCAACATC c.2237_2255delinsAATTAAGAGAAGCAACATC (p.Glu746=) c.*28+1846_*28+1864delinsAATTAAGAGAAGCAACATC (n.*28+1846_*28+1864delinsAATTAAGAGAAGCAACATC) c.2102_2120delinsAATTAAGAGAAGCAACATC (p.Glu701=) c.1436_1454delinsAATTAAGAGAAGCAACATC (p.Glu479=) | |
7 | g.55174774_55174793delinsTC | CA180811 | EGFR | c.2078_2097delinsTC (p.Glu693_Ser699delinsVal) c.586_605delinsTC c.2237_2256delinsTC (p.Glu746_Ser752delinsVal) c.*28+1846_*28+1865delinsTC (n.*28+1846_*28+1865delinsTC) c.2102_2121delinsTC (p.Glu701_Ser707delinsVal) c.1436_1455delinsTC (p.Glu479_Ser485delinsVal) | ClinVar dbSNP COSMIC |
7 | g.55174774_55174793delinsTG | CA645561509 | EGFR | c.2078_2097delinsTG (p.Glu693_Ser699delinsVal) c.586_605delinsTG c.2237_2256delinsTG (p.Glu746_Ser752delinsVal) c.*28+1846_*28+1865delinsTG (n.*28+1846_*28+1865delinsTG) c.2102_2121delinsTG (p.Glu701_Ser707delinsVal) c.1436_1455delinsTG (p.Glu479_Ser485delinsVal) | dbSNP COSMIC |
7 | g.55174774_55174794delinsTCT | CA180622 | EGFR | c.2078_2098delinsTCT (p.Glu693_Pro700delinsValSer) c.586_606delinsTCT c.2237_2257delinsTCT (p.Glu746_Pro753delinsValSer) c.*28+1846_*28+1866delinsTCT (n.*28+1846_*28+1866delinsTCT) c.2102_2122delinsTCT (p.Glu701_Pro708delinsValSer) c.1436_1456delinsTCT (p.Glu479_Pro486delinsValSer) | ClinVar dbSNP COSMIC |
7 | g.55174774_55174795delinsTTCA | CA645561510 | EGFR | c.2078_2099delinsTTCA (p.Glu693_Pro700delinsValGln) c.586_607delinsTTCA c.2237_2258delinsTTCA (p.Glu746_Pro753delinsValGln) c.*28+1846_*28+1867delinsTTCA (n.*28+1846_*28+1867delinsTTCA) c.2102_2123delinsTTCA (p.Glu701_Pro708delinsValGln) c.1436_1457delinsTTCA (p.Glu479_Pro486delinsValGln) | dbSNP COSMIC |
7 | g.55174776_55174799del | CA645561506 | EGFR | c.2080_2103del (p.Leu694_Lys701del) c.588_611del c.2239_2262del (p.Leu747_Lys754del) c.*28+1848_*28+1871del (n.*28+1848_*28+1871del) c.2104_2127del (p.Leu702_Lys709del) c.1438_1461del (p.Leu480_Lys487del) | COSMIC |
7 | g.55174774_55174800delinsCTTCTCTTAATT | CA891842012 | EGFR | c.2078_2104delinsCTTCTCTTAATT (p.Glu693_Ala702delinsAlaSerLeuAsnSer) c.586_612delinsCTTCTCTTAATT c.2237_2263delinsCTTCTCTTAATT (p.Glu746_Ala755delinsAlaSerLeuAsnSer) c.*28+1846_*28+1872delinsCTTCTCTTAATT (n.*28+1846_*28+1872delinsCTTCTCTTAATT) c.2102_2128delinsCTTCTCTTAATT (p.Glu701_Ala710delinsAlaSerLeuAsnSer) c.1436_1462delinsCTTCTCTTAATT (p.Glu479_Ala488delinsAlaSerLeuAsnSer) | |
7 | g.55174775A>C | CA367584151 | EGFR | c.2079A>C (p.Glu693Asp) c.587A>C c.2238A>C (p.Glu746Asp) c.*28+1847A>C (n.*28+1847A>C) c.2103A>C (p.Glu701Asp) c.1437A>C (p.Glu479Asp) | |
7 | g.55174775A>G | CA454979478 | EGFR | c.2079A>G (p.Glu693=) c.587A>G c.2238A>G (p.Glu746=) c.*28+1847A>G (n.*28+1847A>G) c.2103A>G (p.Glu701=) c.1437A>G (p.Glu479=) | |
7 | g.55174775A>T | CA367584152 | EGFR | c.2079A>T (p.Glu693Asp) c.587A>T c.2238A>T (p.Glu746Asp) c.*28+1847A>T (n.*28+1847A>T) c.2103A>T (p.Glu701Asp) c.1437A>T (p.Glu479Asp) | |
7 | g.55174775_55174785delinsGC | CA181028 | EGFR | c.2079_2089delinsGC (p.Leu694_Ala697delinsPro) c.587_597delinsGC c.2238_2248delinsGC (p.Leu747_Ala750delinsPro) c.*28+1847_*28+1857delinsGC (n.*28+1847_*28+1857delinsGC) c.2103_2113delinsGC (p.Leu702_Ala705delinsPro) c.1437_1447delinsGC (p.Leu480_Ala483delinsPro) | ClinVar dbSNP COSMIC |
7 | g.55174775_55174785delinsTC | CA645561522 | EGFR | c.2079_2089delinsTC (p.Glu693_Ala697delinsAspPro) c.587_597delinsTC c.2238_2248delinsTC (p.Glu746_Ala750delinsAspPro) c.*28+1847_*28+1857delinsTC (n.*28+1847_*28+1857delinsTC) c.2103_2113delinsTC (p.Glu701_Ala705delinsAspPro) c.1437_1447delinsTC (p.Glu479_Ala483delinsAspPro) | dbSNP COSMIC |
7 | g.55174775_55174785delinsATTAAGAGAAG | CA1708918332 | EGFR | c.2079_2089delinsATTAAGAGAAG (p.Glu693=) c.587_597delinsATTAAGAGAAG c.2238_2248delinsATTAAGAGAAG (p.Glu746=) c.*28+1847_*28+1857delinsATTAAGAGAAG (n.*28+1847_*28+1857delinsATTAAGAGAAG) c.2103_2113delinsATTAAGAGAAG (p.Glu701=) c.1437_1447delinsATTAAGAGAAG (p.Glu479=) | |
7 | g.55174776_55174787del | CA891842014 | EGFR | c.2080_2091del (p.Leu694_Ala697del) c.588_599del c.2239_2250del (p.Leu747_Ala750del) c.*28+1848_*28+1859del (n.*28+1848_*28+1859del) c.2104_2115del (p.Leu702_Ala705del) c.1438_1449del (p.Leu480_Ala483del) | |
7 | g.55174775_55174788delinsGC | CA180573 | EGFR | c.2079_2092delinsGC (p.Leu694_Thr698delinsPro) c.587_600delinsGC c.2238_2251delinsGC (p.Leu747_Thr751delinsPro) c.*28+1847_*28+1860delinsGC (n.*28+1847_*28+1860delinsGC) c.2103_2116delinsGC (p.Leu702_Thr706delinsPro) c.1437_1450delinsGC (p.Leu480_Thr484delinsPro) | ClinVar dbSNP COSMIC |
7 | g.55174775_55174788delinsATTAAGAGAAGCAA | CA1708918335 | EGFR | c.2079_2092delinsATTAAGAGAAGCAA (p.Glu693=) c.587_600delinsATTAAGAGAAGCAA c.2238_2251delinsATTAAGAGAAGCAA (p.Glu746=) c.*28+1847_*28+1860delinsATTAAGAGAAGCAA (n.*28+1847_*28+1860delinsATTAAGAGAAGCAA) c.2103_2116delinsATTAAGAGAAGCAA (p.Glu701=) c.1437_1450delinsATTAAGAGAAGCAA (p.Glu479=) | |
7 | g.55174775_55174789delinsGCA | CA645561518 | EGFR | c.2079_2093delinsGCA (p.Leu694_Thr698delinsGln) c.587_601delinsGCA c.2238_2252delinsGCA (p.Leu747_Thr751delinsGln) c.*28+1847_*28+1861delinsGCA (n.*28+1847_*28+1861delinsGCA) c.2103_2117delinsGCA (p.Leu702_Thr706delinsGln) c.1437_1451delinsGCA (p.Leu480_Thr484delinsGln) | dbSNP COSMIC |
7 | g.55174777_55174791del | CA180569 | EGFR | c.2081_2095del (p.Leu694_Thr698del) c.589_603del c.2240_2254del (p.Leu747_Thr751del) c.*28+1849_*28+1863del (n.*28+1849_*28+1863del) c.2105_2119del (p.Leu702_Thr706del) c.1439_1453del (p.Leu480_Thr484del) | ClinVar dbSNP COSMIC COSMIC |
7 | g.55174775_55174792del | CA158932595 | EGFR | c.2079_2096del (p.Glu693_Ser699delinsAsp) c.587_604del c.2238_2255del (p.Glu746_Ser752delinsAsp) c.*28+1847_*28+1864del (n.*28+1847_*28+1864del) c.2103_2120del (p.Glu701_Ser707delinsAsp) c.1437_1454del (p.Glu479_Ser485delinsAsp) | dbSNP COSMIC |
7 | g.55174775_55174792delinsGCAACA | CA645561520 | EGFR | c.2079_2096delinsGCAACA (p.Leu694_Ser699delinsGlnHis) c.587_604delinsGCAACA c.2238_2255delinsGCAACA (p.Leu747_Ser752delinsGlnHis) c.*28+1847_*28+1864delinsGCAACA (n.*28+1847_*28+1864delinsGCAACA) c.2103_2120delinsGCAACA (p.Leu702_Ser707delinsGlnHis) c.1437_1454delinsGCAACA (p.Leu480_Ser485delinsGlnHis) | dbSNP COSMIC |
7 | g.55174775_55174793delinsGCAA | CA645561521 | EGFR | c.2079_2097delinsGCAA (p.Leu694_Ser699delinsGln) c.587_605delinsGCAA c.2238_2256delinsGCAA (p.Leu747_Ser752delinsGln) c.*28+1847_*28+1865delinsGCAA (n.*28+1847_*28+1865delinsGCAA) c.2103_2121delinsGCAA (p.Leu702_Ser707delinsGln) c.1437_1455delinsGCAA (p.Leu480_Ser485delinsGln) | dbSNP COSMIC |
7 | g.55174775_55174793delinsATTAAGAGAAGCAACATCT | CA1708918336 | EGFR | c.2079_2097delinsATTAAGAGAAGCAACATCT (p.Glu693=) c.587_605delinsATTAAGAGAAGCAACATCT c.2238_2256delinsATTAAGAGAAGCAACATCT (p.Glu746=) c.*28+1847_*28+1865delinsATTAAGAGAAGCAACATCT (n.*28+1847_*28+1865delinsATTAAGAGAAGCAACATCT) c.2103_2121delinsATTAAGAGAAGCAACATCT (p.Glu701=) c.1437_1455delinsATTAAGAGAAGCAACATCT (p.Glu479=) | |
7 | g.55174775_55174794delinsATTAAGAGAAGCAACATCTC | CA1708918334 | EGFR | c.2079_2098delinsATTAAGAGAAGCAACATCTC (p.Glu693=) c.587_606delinsATTAAGAGAAGCAACATCTC c.2238_2257delinsATTAAGAGAAGCAACATCTC (p.Glu746=) c.*28+1847_*28+1866delinsATTAAGAGAAGCAACATCTC (n.*28+1847_*28+1866delinsATTAAGAGAAGCAACATCTC) c.2103_2122delinsATTAAGAGAAGCAACATCTC (p.Glu701=) c.1437_1456delinsATTAAGAGAAGCAACATCTC (p.Glu479=) | |
7 | g.55174775_55174795del | CA645561519 | EGFR | c.2079_2099del (p.Leu694_Pro700del) c.587_607del c.2238_2258del (p.Leu747_Pro753del) c.*28+1847_*28+1867del (n.*28+1847_*28+1867del) c.2103_2123del (p.Leu702_Pro708del) c.1437_1457del (p.Leu480_Pro486del) | COSMIC |
7 | g.55174775_55174795delinsATTAAGAGAAGCAACATCTCC | CA1708918337 | EGFR | c.2079_2099delinsATTAAGAGAAGCAACATCTCC (p.Glu693=) c.587_607delinsATTAAGAGAAGCAACATCTCC c.2238_2258delinsATTAAGAGAAGCAACATCTCC (p.Glu746=) c.*28+1847_*28+1867delinsATTAAGAGAAGCAACATCTCC (n.*28+1847_*28+1867delinsATTAAGAGAAGCAACATCTCC) c.2103_2123delinsATTAAGAGAAGCAACATCTCC (p.Glu701=) c.1437_1457delinsATTAAGAGAAGCAACATCTCC (p.Glu479=) | |
7 | g.55174775_55174801delinsATTAAGAGAAGCAACATCTCCGAAAGC | CA1708918333 | EGFR | c.2079_2105delinsATTAAGAGAAGCAACATCTCCGAAAGC (p.Glu693=) c.587_613delinsATTAAGAGAAGCAACATCTCCGAAAGC c.2238_2264delinsATTAAGAGAAGCAACATCTCCGAAAGC (p.Glu746=) c.*28+1847_*28+1873delinsATTAAGAGAAGCAACATCTCCGAAAGC (n.*28+1847_*28+1873delinsATTAAGAGAAGCAACATCTCCGAAAGC) c.2103_2129delinsATTAAGAGAAGCAACATCTCCGAAAGC (p.Glu701=) c.1437_1463delinsATTAAGAGAAGCAACATCTCCGAAAGC (p.Glu479=) | |
7 | g.55174776T>A | CA367584154 | EGFR | c.2080T>A (p.Leu694Ile) c.588T>A c.2239T>A (p.Leu747Ile) c.*28+1848T>A (n.*28+1848T>A) c.2104T>A (p.Leu702Ile) c.1438T>A (p.Leu480Ile) | |
7 | g.55174776T>C | CA135797 | EGFR | c.2080T>C (p.Leu694=) c.588T>C c.2239T>C (p.Leu747=) c.*28+1848T>C (n.*28+1848T>C) c.2104T>C (p.Leu702=) c.1438T>C (p.Leu480=) | ClinVar dbSNP |
7 | g.55174776T>G | CA367584153 | EGFR | c.2080T>G (p.Leu694Val) c.588T>G c.2239T>G (p.Leu747Val) c.*28+1848T>G (n.*28+1848T>G) c.2104T>G (p.Leu702Val) c.1438T>G (p.Leu480Val) | ClinVar dbSNP |
7 | g.55174776T= | CA1708918340 | EGFR | c.2080T= (p.Leu694=) c.588T= c.2239T= (p.Leu747=) c.*28+1848T= (n.*28+1848T=) c.2104T= (p.Leu702=) c.1438T= (p.Leu480=) | |
7 | g.55174776_55174777delinsCC | CA135800 | EGFR | c.2080_2081delinsCC (p.Leu694Pro) c.588_589delinsCC c.2239_2240delinsCC (p.Leu747Pro) c.*28+1848_*28+1849delinsCC (n.*28+1848_*28+1849delinsCC) c.2104_2105delinsCC (p.Leu702Pro) c.1438_1439delinsCC (p.Leu480Pro) | ClinVar dbSNP COSMIC |
7 | g.55174776_55174777delinsTT | CA1708918339 | EGFR | c.2080_2081delinsTT (p.Leu694=) c.588_589delinsTT c.2239_2240delinsTT (p.Leu747=) c.*28+1848_*28+1849delinsTT (n.*28+1848_*28+1849delinsTT) c.2104_2105delinsTT (p.Leu702=) c.1438_1439delinsTT (p.Leu480=) | |
7 | g.55174776_55174785del | CA891842023 | EGFR | c.2080_2089del (p.Leu694GlnfsTer16) c.588_597del c.2239_2248del (p.Leu747GlnfsTer16) c.*28+1848_*28+1857del (n.*28+1848_*28+1857del) c.2104_2113del (p.Leu702GlnfsTer16) c.1438_1447del (p.Leu480GlnfsTer16) | |
7 | g.55174776_55174785delinsC | CA180612 | EGFR | c.2080_2089delinsC (p.Leu694_Ala697delinsPro) c.588_597delinsC c.2239_2248delinsC (p.Leu747_Ala750delinsPro) c.*28+1848_*28+1857delinsC (n.*28+1848_*28+1857delinsC) c.2104_2113delinsC (p.Leu702_Ala705delinsPro) c.1438_1447delinsC (p.Leu480_Ala483delinsPro) | ClinVar dbSNP COSMIC |
7 | g.55174776_55174785delinsTTAAGAGAAG | CA1708918338 | EGFR | c.2080_2089delinsTTAAGAGAAG (p.Leu694=) c.588_597delinsTTAAGAGAAG c.2239_2248delinsTTAAGAGAAG (p.Leu747=) c.*28+1848_*28+1857delinsTTAAGAGAAG (n.*28+1848_*28+1857delinsTTAAGAGAAG) c.2104_2113delinsTTAAGAGAAG (p.Leu702=) c.1438_1447delinsTTAAGAGAAG (p.Leu480=) | |
7 | g.55174776_55174787delinsCCG | CA645561526 | EGFR | c.2080_2091delinsCCG (p.Leu694_Ala697delinsPro) c.588_599delinsCCG c.2239_2250delinsCCG (p.Leu747_Ala750delinsPro) c.*28+1848_*28+1859delinsCCG (n.*28+1848_*28+1859delinsCCG) c.2104_2115delinsCCG (p.Leu702_Ala705delinsPro) c.1438_1449delinsCCG (p.Leu480_Ala483delinsPro) | dbSNP COSMIC |
7 | g.55174776_55174788delinsC | CA126716 | EGFR | c.2080_2092delinsC (p.Leu694_Thr698delinsPro) c.588_600delinsC c.2239_2251delinsC (p.Leu747_Thr751delinsPro) c.*28+1848_*28+1860delinsC (n.*28+1848_*28+1860delinsC) c.2104_2116delinsC (p.Leu702_Thr706delinsPro) c.1438_1450delinsC (p.Leu480_Thr484delinsPro) | ClinVar dbSNP COSMIC |
7 | g.55174776_55174788delinsTTAAGAGAAGCAA | CA1708918341 | EGFR | c.2080_2092delinsTTAAGAGAAGCAA (p.Leu694=) c.588_600delinsTTAAGAGAAGCAA c.2239_2251delinsTTAAGAGAAGCAA (p.Leu747=) c.*28+1848_*28+1860delinsTTAAGAGAAGCAA (n.*28+1848_*28+1860delinsTTAAGAGAAGCAA) c.2104_2116delinsTTAAGAGAAGCAA (p.Leu702=) c.1438_1450delinsTTAAGAGAAGCAA (p.Leu480=) | |
7 | g.55174776_55174789delinsCA | CA645561530 | EGFR | c.2080_2093delinsCA (p.Leu694_Thr698delinsGln) c.588_601delinsCA c.2239_2252delinsCA (p.Leu747_Thr751delinsGln) c.*28+1848_*28+1861delinsCA (n.*28+1848_*28+1861delinsCA) c.2104_2117delinsCA (p.Leu702_Thr706delinsGln) c.1438_1451delinsCA (p.Leu480_Thr484delinsGln) | dbSNP COSMIC COSMIC |
7 | g.55174776_55174790delinsAAT | CA645561527 | EGFR | c.2080_2094delinsAAT (p.Leu694_Thr698delinsAsn) c.588_602delinsAAT c.2239_2253delinsAAT (p.Leu747_Thr751delinsAsn) c.*28+1848_*28+1862delinsAAT (n.*28+1848_*28+1862delinsAAT) c.2104_2118delinsAAT (p.Leu702_Thr706delinsAsn) c.1438_1452delinsAAT (p.Leu480_Thr484delinsAsn) | COSMIC |
7 | g.55174776_55174790delinsGCT | CA645561529 | EGFR | c.2080_2094delinsGCT (p.Leu694_Thr698delinsAla) c.588_602delinsGCT c.2239_2253delinsGCT (p.Leu747_Thr751delinsAla) c.*28+1848_*28+1862delinsGCT (n.*28+1848_*28+1862delinsGCT) c.2104_2118delinsGCT (p.Leu702_Thr706delinsAla) c.1438_1452delinsGCT (p.Leu480_Thr484delinsAla) | dbSNP COSMIC |
7 | g.55174776_55174790delinsCCAACG | CA645561531 | EGFR | c.2080_2094delinsCCAACG (p.Leu694_Ala697delinsPro) c.588_602delinsCCAACG c.2239_2253delinsCCAACG (p.Leu747_Ala750delinsPro) c.*28+1848_*28+1862delinsCCAACG (n.*28+1848_*28+1862delinsCCAACG) c.2104_2118delinsCCAACG (p.Leu702_Ala705delinsPro) c.1438_1452delinsCCAACG (p.Leu480_Ala483delinsPro) | dbSNP COSMIC |
7 | g.55174776_55174792delinsCAACA | CA645561528 | EGFR | c.2080_2096delinsCAACA (p.Leu694_Ser699delinsGlnHis) c.588_604delinsCAACA c.2239_2255delinsCAACA (p.Leu747_Ser752delinsGlnHis) c.*28+1848_*28+1864delinsCAACA (n.*28+1848_*28+1864delinsCAACA) c.2104_2120delinsCAACA (p.Leu702_Ser707delinsGlnHis) c.1438_1454delinsCAACA (p.Leu480_Ser485delinsGlnHis) | dbSNP COSMIC |
7 | g.55174776_55174792delinsCCACA | CA2573129747 | EGFR | c.2080_2096delinsCCACA (p.Leu694_Ser699delinsProHis) c.588_604delinsCCACA c.2239_2255delinsCCACA (p.Leu747_Ser752delinsProHis) c.*28+1848_*28+1864delinsCCACA (n.*28+1848_*28+1864delinsCCACA) c.2104_2120delinsCCACA (p.Leu702_Ser707delinsProHis) c.1438_1454delinsCCACA (p.Leu480_Ser485delinsProHis) | |
7 | g.55174776_55174793del | CA180566 | EGFR | c.2080_2097del (p.Leu694_Ser699del) c.588_605del c.2239_2256del (p.Leu747_Ser752del) c.*28+1848_*28+1865del (n.*28+1848_*28+1865del) c.2104_2121del (p.Leu702_Ser707del) c.1438_1455del (p.Leu480_Ser485del) | ClinVar dbSNP COSMIC |
7 | g.55174776_55174793delinsCAA | CA645561524 | EGFR | c.2080_2097delinsCAA (p.Leu694_Ser699delinsGln) c.588_605delinsCAA c.2239_2256delinsCAA (p.Leu747_Ser752delinsGln) c.*28+1848_*28+1865delinsCAA (n.*28+1848_*28+1865delinsCAA) c.2104_2121delinsCAA (p.Leu702_Ser707delinsGln) c.1438_1455delinsCAA (p.Leu480_Ser485delinsGln) | ClinVar dbSNP COSMIC |
7 | g.55174776_55174794delinsA | CA180819 | EGFR | c.2080_2098delinsA (p.Leu694_Pro700delinsThr) c.588_606delinsA c.2239_2257delinsA (p.Leu747_Pro753delinsThr) c.*28+1848_*28+1866delinsA (n.*28+1848_*28+1866delinsA) c.2104_2122delinsA (p.Leu702_Pro708delinsThr) c.1438_1456delinsA (p.Leu480_Pro486delinsThr) | ClinVar dbSNP |
7 | g.55174776_55174794delinsCAAT | CA180861 | EGFR | c.2080_2098delinsCAAT (p.Leu694_Pro700delinsGlnSer) c.588_606delinsCAAT c.2239_2257delinsCAAT (p.Leu747_Pro753delinsGlnSer) c.*28+1848_*28+1866delinsCAAT (n.*28+1848_*28+1866delinsCAAT) c.2104_2122delinsCAAT (p.Leu702_Pro708delinsGlnSer) c.1438_1456delinsCAAT (p.Leu480_Pro486delinsGlnSer) | ClinVar dbSNP |
7 | g.55174776_55174794delinsTTAAGAGAAGCAACATCTC | CA1708918342 | EGFR | c.2080_2098delinsTTAAGAGAAGCAACATCTC (p.Leu694=) c.588_606delinsTTAAGAGAAGCAACATCTC c.2239_2257delinsTTAAGAGAAGCAACATCTC (p.Leu747=) c.*28+1848_*28+1866delinsTTAAGAGAAGCAACATCTC (n.*28+1848_*28+1866delinsTTAAGAGAAGCAACATCTC) c.2104_2122delinsTTAAGAGAAGCAACATCTC (p.Leu702=) c.1438_1456delinsTTAAGAGAAGCAACATCTC (p.Leu480=) | |
7 | g.55174776_55174795delinsCA | CA158932624 | EGFR | c.2080_2099delinsCA (p.Leu694_Pro700delinsGln) c.588_607delinsCA c.2239_2258delinsCA (p.Leu747_Pro753delinsGln) c.*28+1848_*28+1867delinsCA (n.*28+1848_*28+1867delinsCA) c.2104_2123delinsCA (p.Leu702_Pro708delinsGln) c.1438_1457delinsCA (p.Leu480_Pro486delinsGln) | dbSNP COSMIC |
7 | g.55174776_55174796del | CA891842022 | EGFR | c.2080_2100del (p.Leu694_Pro700del) c.588_608del c.2239_2259del (p.Leu747_Pro753del) c.*28+1848_*28+1868del (n.*28+1848_*28+1868del) c.2104_2124del (p.Leu702_Pro708del) c.1438_1458del (p.Leu480_Pro486del) | |
7 | g.55174776_55174796delinsCAA | CA645561523 | EGFR | c.2080_2100delinsCAA (p.Leu694_Pro700delinsGln) c.588_608delinsCAA c.2239_2259delinsCAA (p.Leu747_Pro753delinsGln) c.*28+1848_*28+1868delinsCAA (n.*28+1848_*28+1868delinsCAA) c.2104_2124delinsCAA (p.Leu702_Pro708delinsGln) c.1438_1458delinsCAA (p.Leu480_Pro486delinsGln) | COSMIC |
7 | g.55174776_55174797delinsGCAATATCTCCGG | CA891842021 | EGFR | c.2080_2101delinsGCAATATCTCCGG (p.Leu694_Lys701delinsAlaIleSerProGlu) c.588_609delinsGCAATATCTCCGG c.2239_2260delinsGCAATATCTCCGG (p.Leu747_Lys754delinsAlaIleSerProGlu) c.*28+1848_*28+1869delinsGCAATATCTCCGG (n.*28+1848_*28+1869delinsGCAATATCTCCGG) c.2104_2125delinsGCAATATCTCCGG (p.Leu702_Lys709delinsAlaIleSerProGlu) c.1438_1459delinsGCAATATCTCCGG (p.Leu480_Lys487delinsAlaIleSerProGlu) | |
7 | g.55174776_55174798delinsGCCAACAAGGG | CA645561525 | EGFR | c.2080_2102delinsGCCAACAAGGG (p.Leu694_Lys701delinsAlaAsnLysGly) c.588_610delinsGCCAACAAGGG c.2239_2261delinsGCCAACAAGGG (p.Leu747_Lys754delinsAlaAsnLysGly) c.*28+1848_*28+1870delinsGCCAACAAGGG (n.*28+1848_*28+1870delinsGCCAACAAGGG) c.2104_2126delinsGCCAACAAGGG (p.Leu702_Lys709delinsAlaAsnLysGly) c.1438_1460delinsGCCAACAAGGG (p.Leu480_Lys487delinsAlaAsnLysGly) | dbSNP COSMIC |
7 | g.55174776_55174801delinsGCCAA | CA645561532 | EGFR | c.2080_2105delinsGCCAA (p.Leu694_Ala702delinsAlaAsn) c.588_613delinsGCCAA c.2239_2264delinsGCCAA (p.Leu747_Ala755delinsAlaAsn) c.*28+1848_*28+1873delinsGCCAA (n.*28+1848_*28+1873delinsGCCAA) c.2104_2129delinsGCCAA (p.Leu702_Ala710delinsAlaAsn) c.1438_1463delinsGCCAA (p.Leu480_Ala488delinsAlaAsn) | COSMIC |
7 | g.55174776_55174801delinsACGAGAGA | CA181041 | EGFR | c.2080_2105delinsACGAGAGA (p.Leu694_Ala702delinsThrArgAsp) c.588_613delinsACGAGAGA c.2239_2264delinsACGAGAGA (p.Leu747_Ala755delinsThrArgAsp) c.*28+1848_*28+1873delinsACGAGAGA (n.*28+1848_*28+1873delinsACGAGAGA) c.2104_2129delinsACGAGAGA (p.Leu702_Ala710delinsThrArgAsp) c.1438_1463delinsACGAGAGA (p.Leu480_Ala488delinsThrArgAsp) | ClinVar dbSNP |
7 | g.55174777T>A | CA367584156 | EGFR | c.2081T>A (p.Leu694Ter) c.589T>A c.2240T>A (p.Leu747Ter) c.*28+1849T>A (n.*28+1849T>A) c.2105T>A (p.Leu702Ter) c.1439T>A (p.Leu480Ter) | |
7 | g.55174777T>C | CA135803 | EGFR | c.2081T>C (p.Leu694Ser) c.589T>C c.2240T>C (p.Leu747Ser) c.*28+1849T>C (n.*28+1849T>C) c.2105T>C (p.Leu702Ser) c.1439T>C (p.Leu480Ser) | ClinVar dbSNP COSMIC |
7 | g.55174777T>G | CA367584155 | EGFR | c.2081T>G (p.Leu694Ter) c.589T>G c.2240T>G (p.Leu747Ter) c.*28+1849T>G (n.*28+1849T>G) c.2105T>G (p.Leu702Ter) c.1439T>G (p.Leu480Ter) | |
7 | g.55174777T= | CA1708918343 | EGFR | c.2081T= (p.Leu694=) c.589T= c.2240T= (p.Leu747=) c.*28+1849T= (n.*28+1849T=) c.2105T= (p.Leu702=) c.1439T= (p.Leu480=) | |
7 | g.55174777_55174785del | CA135806 | EGFR | c.2081_2089del (p.Leu694_Ala697delinsSer) c.589_597del c.2240_2248del (p.Leu747_Ala750delinsSer) c.*28+1849_*28+1857del (n.*28+1849_*28+1857del) c.2105_2113del (p.Leu702_Ala705delinsSer) c.1439_1447del (p.Leu480_Ala483delinsSer) | ClinVar dbSNP COSMIC |
7 | g.55174777_55174788del | CA158932632 | EGFR | c.2081_2092del (p.Leu694_Thr698delinsSer) c.589_600del c.2240_2251del (p.Leu747_Thr751delinsSer) c.*28+1849_*28+1860del (n.*28+1849_*28+1860del) c.2105_2116del (p.Leu702_Thr706delinsSer) c.1439_1450del (p.Leu480_Thr484delinsSer) | dbSNP COSMIC |
7 | g.55174777_55174794del | CA126710 | EGFR | c.2081_2098del (p.Leu694_Pro700delinsSer) c.589_606del c.2240_2257del (p.Leu747_Pro753delinsSer) c.*28+1849_*28+1866del (n.*28+1849_*28+1866del) c.2105_2122del (p.Leu702_Pro708delinsSer) c.1439_1456del (p.Leu480_Pro486delinsSer) | ClinVar dbSNP COSMIC COSMIC |
7 | g.55174777_55174796delinsCT | CA891842026 | EGFR | c.2081_2100delinsCT (p.Leu694_Pro700delinsSer) c.589_608delinsCT c.2240_2259delinsCT (p.Leu747_Pro753delinsSer) c.*28+1849_*28+1868delinsCT (n.*28+1849_*28+1868delinsCT) c.2105_2124delinsCT (p.Leu702_Pro708delinsSer) c.1439_1458delinsCT (p.Leu480_Pro486delinsSer) | |
7 | g.55174777_55174798delinsCGAC | CA645561534 | EGFR | c.2081_2102delinsCGAC (p.Leu694_Lys701delinsSerThr) c.589_610delinsCGAC c.2240_2261delinsCGAC (p.Leu747_Lys754delinsSerThr) c.*28+1849_*28+1870delinsCGAC (n.*28+1849_*28+1870delinsCGAC) c.2105_2126delinsCGAC (p.Leu702_Lys709delinsSerThr) c.1439_1460delinsCGAC (p.Leu480_Lys487delinsSerThr) | dbSNP COSMIC |
7 | g.55174777_55174801delinsCGAAAGA | CA891842025 | EGFR | c.2081_2105delinsCGAAAGA (p.Leu694_Ala702delinsSerLysAsp) c.589_613delinsCGAAAGA c.2240_2264delinsCGAAAGA (p.Leu747_Ala755delinsSerLysAsp) c.*28+1849_*28+1873delinsCGAAAGA (n.*28+1849_*28+1873delinsCGAAAGA) c.2105_2129delinsCGAAAGA (p.Leu702_Ala710delinsSerLysAsp) c.1439_1463delinsCGAAAGA (p.Leu480_Ala488delinsSerLysAsp) | |
7 | g.55174777_55174801delinsCGAAAGG | CA645561535 | EGFR | c.2081_2105delinsCGAAAGG (p.Leu694_Ala702delinsSerLysGly) c.589_613delinsCGAAAGG c.2240_2264delinsCGAAAGG (p.Leu747_Ala755delinsSerLysGly) c.*28+1849_*28+1873delinsCGAAAGG (n.*28+1849_*28+1873delinsCGAAAGG) c.2105_2129delinsCGAAAGG (p.Leu702_Ala710delinsSerLysGly) c.1439_1463delinsCGAAAGG (p.Leu480_Ala488delinsSerLysGly) | dbSNP COSMIC |
7 | g.55174778A>C | CA367584157 | EGFR | c.2082A>C (p.Leu694Phe) c.590A>C c.2241A>C (p.Leu747Phe) c.*28+1850A>C (n.*28+1850A>C) c.2106A>C (p.Leu702Phe) c.1440A>C (p.Leu480Phe) | |
7 | g.55174778A>G | CA454979509 | EGFR | c.2082A>G (p.Leu694=) c.590A>G c.2241A>G (p.Leu747=) c.*28+1850A>G (n.*28+1850A>G) c.2106A>G (p.Leu702=) c.1440A>G (p.Leu480=) | dbSNP |
7 | g.55174778A>T | CA367584158 | EGFR | c.2082A>T (p.Leu694Phe) c.590A>T c.2241A>T (p.Leu747Phe) c.*28+1850A>T (n.*28+1850A>T) c.2106A>T (p.Leu702Phe) c.1440A>T (p.Leu480Phe) | dbSNP |
7 | g.55174778_55174781delinsAAGA | CA1708918344 | EGFR | c.2082_2085delinsAAGA (p.Leu694=) c.590_593delinsAAGA c.2241_2244delinsAAGA (p.Leu747=) c.*28+1850_*28+1853delinsAAGA (n.*28+1850_*28+1853delinsAAGA) c.2106_2109delinsAAGA (p.Leu702=) c.1440_1443delinsAAGA (p.Leu480=) | |
7 | g.55174778_55174781delinsCCCG | CA158932639 | EGFR | c.2082_2085delinsCCCG (p.Leu694_Arg695delinsPhePro) c.590_593delinsCCCG c.2241_2244delinsCCCG (p.Leu747_Arg748delinsPhePro) c.*28+1850_*28+1853delinsCCCG (n.*28+1850_*28+1853delinsCCCG) c.2106_2109delinsCCCG (p.Leu702_Arg703delinsPhePro) c.1440_1443delinsCCCG (p.Leu480_Arg481delinsPhePro) | dbSNP COSMIC |
7 | g.55174779_55174788del | CA891842027 | EGFR | c.2083_2092del (p.Arg695HisfsTer15) c.591_600del c.2242_2251del (p.Arg748HisfsTer15) c.*28+1851_*28+1860del (n.*28+1851_*28+1860del) c.2107_2116del (p.Arg703HisfsTer15) c.1441_1450del (p.Arg481HisfsTer15) | |
7 | g.55174779A>C | CA454979513 | EGFR | c.2083A>C (p.Arg695=) c.591A>C c.2242A>C (p.Arg748=) c.*28+1851A>C (n.*28+1851A>C) c.2107A>C (p.Arg703=) c.1441A>C (p.Arg481=) | |
7 | g.55174779A>G | CA367584159 | EGFR | c.2083A>G (p.Arg695Gly) c.591A>G c.2242A>G (p.Arg748Gly) c.*28+1851A>G (n.*28+1851A>G) c.2107A>G (p.Arg703Gly) c.1441A>G (p.Arg481Gly) | dbSNP |
7 | g.55174779A>T | CA367584160 | EGFR | c.2083A>T (p.Arg695Ter) c.591A>T c.2242A>T (p.Arg748Ter) c.*28+1851A>T (n.*28+1851A>T) c.2107A>T (p.Arg703Ter) c.1441A>T (p.Arg481Ter) | dbSNP |
7 | g.55174780G>A | CA367584163 | EGFR | c.2084G>A (p.Arg695Lys) c.592G>A c.2243G>A (p.Arg748Lys) c.*28+1852G>A (n.*28+1852G>A) c.2108G>A (p.Arg703Lys) c.1442G>A (p.Arg481Lys) | dbSNP gnomAD v2 gnomAD v4 COSMIC |
7 | g.55174780G>C | CA367584161 | EGFR | c.2084G>C (p.Arg695Thr) c.592G>C c.2243G>C (p.Arg748Thr) c.*28+1852G>C (n.*28+1852G>C) c.2108G>C (p.Arg703Thr) c.1442G>C (p.Arg481Thr) | dbSNP |
7 | g.55174780G= | CA1708918345 | EGFR | c.2084G= (p.Arg695=) c.592G= c.2243G= (p.Arg748=) c.*28+1852G= (n.*28+1852G=) c.2108G= (p.Arg703=) c.1442G= (p.Arg481=) | |
7 | g.55174780G>T | CA367584162 | EGFR | c.2084G>T (p.Arg695Ile) c.592G>T c.2243G>T (p.Arg748Ile) c.*28+1852G>T (n.*28+1852G>T) c.2108G>T (p.Arg703Ile) c.1442G>T (p.Arg481Ile) | dbSNP COSMIC |
7 | g.55174781A= | CA1708918346 | EGFR | c.2085A= (p.Arg695=) c.593A= c.2244A= (p.Arg748=) c.*28+1853A= (n.*28+1853A=) c.2109A= (p.Arg703=) c.1443A= (p.Arg481=) | |
7 | g.55174781A>C | CA367584164 | EGFR | c.2085A>C (p.Arg695Ser) c.593A>C c.2244A>C (p.Arg748Ser) c.*28+1853A>C (n.*28+1853A>C) c.2109A>C (p.Arg703Ser) c.1443A>C (p.Arg481Ser) | |
7 | g.55174781A>G | CA454979521 | EGFR | c.2085A>G (p.Arg695=) c.593A>G c.2244A>G (p.Arg748=) c.*28+1853A>G (n.*28+1853A>G) c.2109A>G (p.Arg703=) c.1443A>G (p.Arg481=) | |
7 | g.55174781A>T | CA367584165 | EGFR | c.2085A>T (p.Arg695Ser) c.593A>T c.2244A>T (p.Arg748Ser) c.*28+1853A>T (n.*28+1853A>T) c.2109A>T (p.Arg703Ser) c.1443A>T (p.Arg481Ser) | dbSNP |
7 | g.55174782G>A | CA367584166 | EGFR | c.2086G>A (p.Glu696Lys) c.594G>A c.2245G>A (p.Glu749Lys) c.*28+1854G>A (n.*28+1854G>A) c.2110G>A (p.Glu704Lys) c.1444G>A (p.Glu482Lys) | |
7 | g.55174782G>C | CA16603146 | EGFR | c.2086G>C (p.Glu696Gln) c.594G>C c.2245G>C (p.Glu749Gln) c.*28+1854G>C (n.*28+1854G>C) c.2110G>C (p.Glu704Gln) c.1444G>C (p.Glu482Gln) | ClinVar dbSNP |
7 | g.55174782G= | CA1708918347 | EGFR | c.2086G= (p.Glu696=) c.594G= c.2245G= (p.Glu749=) c.*28+1854G= (n.*28+1854G=) c.2110G= (p.Glu704=) c.1444G= (p.Glu482=) | |
7 | g.55174782G>T | CA367584167 | EGFR | c.2086G>T (p.Glu696Ter) c.594G>T c.2245G>T (p.Glu749Ter) c.*28+1854G>T (n.*28+1854G>T) c.2110G>T (p.Glu704Ter) c.1444G>T (p.Glu482Ter) | |
7 | g.55174785_55174811del | CA645561536 | EGFR | c.2089_2115del (p.Ala697_Glu705del) c.597_623del c.2248_2274del (p.Ala750_Glu758del) c.*28+1857_*28+1883del (n.*28+1857_*28+1883del) c.2113_2139del (p.Ala705_Glu713del) c.1447_1473del (p.Ala483_Glu491del) | COSMIC |
7 | g.55174783A>C | CA367584170 | EGFR | c.2087A>C (p.Glu696Ala) c.595A>C c.2246A>C (p.Glu749Ala) c.*28+1855A>C (n.*28+1855A>C) c.2111A>C (p.Glu704Ala) c.1445A>C (p.Glu482Ala) | |
7 | g.55174783A>G | CA367584169 | EGFR | c.2087A>G (p.Glu696Gly) c.595A>G c.2246A>G (p.Glu749Gly) c.*28+1855A>G (n.*28+1855A>G) c.2111A>G (p.Glu704Gly) c.1445A>G (p.Glu482Gly) | ClinVar dbSNP COSMIC |
7 | g.55174783A>T | CA367584168 | EGFR | c.2087A>T (p.Glu696Val) c.595A>T c.2246A>T (p.Glu749Val) c.*28+1855A>T (n.*28+1855A>T) c.2111A>T (p.Glu704Val) c.1445A>T (p.Glu482Val) | |
7 | g.55174783_55174801delinsAAGCAACATCTCCGAAAGC | CA1708918348 | EGFR | c.2087_2105delinsAAGCAACATCTCCGAAAGC (p.Glu696=) c.595_613delinsAAGCAACATCTCCGAAAGC c.2246_2264delinsAAGCAACATCTCCGAAAGC (p.Glu749=) c.*28+1855_*28+1873delinsAAGCAACATCTCCGAAAGC (n.*28+1855_*28+1873delinsAAGCAACATCTCCGAAAGC) c.2111_2129delinsAAGCAACATCTCCGAAAGC (p.Glu704=) c.1445_1463delinsAAGCAACATCTCCGAAAGC (p.Glu482=) | |
7 | g.55174787_55174801del | CA645561537 | EGFR | c.2091_2105del (p.Thr698_Ala702del) c.599_613del c.2250_2264del (p.Thr751_Ala755del) c.*28+1859_*28+1873del (n.*28+1859_*28+1873del) c.2115_2129del (p.Thr706_Ala710del) c.1449_1463del (p.Thr484_Ala488del) | dbSNP COSMIC |
7 | g.55174784A= | CA1708918349 | EGFR | c.2088A= (p.Glu696=) c.596A= c.2247A= (p.Glu749=) c.*28+1856A= (n.*28+1856A=) c.2112A= (p.Glu704=) c.1446A= (p.Glu482=) | |
7 | g.55174784A>C | CA367584171 | EGFR | c.2088A>C (p.Glu696Asp) c.596A>C c.2247A>C (p.Glu749Asp) c.*28+1856A>C (n.*28+1856A>C) c.2112A>C (p.Glu704Asp) c.1446A>C (p.Glu482Asp) | dbSNP gnomAD v4 |
7 | g.55174784A>G | CA454979532 | EGFR | c.2088A>G (p.Glu696=) c.596A>G c.2247A>G (p.Glu749=) c.*28+1856A>G (n.*28+1856A>G) c.2112A>G (p.Glu704=) c.1446A>G (p.Glu482=) | ClinVar dbSNP |
7 | g.55174784A>T | CA367584172 | EGFR | c.2088A>T (p.Glu696Asp) c.596A>T c.2247A>T (p.Glu749Asp) c.*28+1856A>T (n.*28+1856A>T) c.2112A>T (p.Glu704Asp) c.1446A>T (p.Glu482Asp) | dbSNP |
7 | g.55174784_55174801del | CA135809 | EGFR | c.2088_2105del (p.Glu696_Ala702delinsAsp) c.596_613del c.2247_2264del (p.Glu749_Ala755delinsAsp) c.*28+1856_*28+1873del (n.*28+1856_*28+1873del) c.2112_2129del (p.Glu704_Ala710delinsAsp) c.1446_1463del (p.Glu482_Ala488delinsAsp) | ClinVar dbSNP |
7 | g.55174785G>A | CA367584173 | EGFR | c.2089G>A (p.Ala697Thr) c.597G>A c.2248G>A (p.Ala750Thr) c.*28+1857G>A (n.*28+1857G>A) c.2113G>A (p.Ala705Thr) c.1447G>A (p.Ala483Thr) | dbSNP |
7 | g.55174785G>C | CA135812 | EGFR | c.2089G>C (p.Ala697Pro) c.597G>C c.2248G>C (p.Ala750Pro) c.*28+1857G>C (n.*28+1857G>C) c.2113G>C (p.Ala705Pro) c.1447G>C (p.Ala483Pro) | ClinVar dbSNP COSMIC |
7 | g.55174785G= | CA1708918350 | EGFR | c.2089G= (p.Ala697=) c.597G= c.2248G= (p.Ala750=) c.*28+1857G= (n.*28+1857G=) c.2113G= (p.Ala705=) c.1447G= (p.Ala483=) | |
7 | g.55174785G>T | CA367584174 | EGFR | c.2089G>T (p.Ala697Ser) c.597G>T c.2248G>T (p.Ala750Ser) c.*28+1857G>T (n.*28+1857G>T) c.2113G>T (p.Ala705Ser) c.1447G>T (p.Ala483Ser) | |
7 | g.55174785_55174801delinsGCAACATCTCCGAAAGC | CA1708918351 | EGFR | c.2089_2105delinsGCAACATCTCCGAAAGC (p.Ala697=) c.597_613delinsGCAACATCTCCGAAAGC c.2248_2264delinsGCAACATCTCCGAAAGC (p.Ala750=) c.*28+1857_*28+1873delinsGCAACATCTCCGAAAGC (n.*28+1857_*28+1873delinsGCAACATCTCCGAAAGC) c.2113_2129delinsGCAACATCTCCGAAAGC (p.Ala705=) c.1447_1463delinsGCAACATCTCCGAAAGC (p.Ala483=) | |
7 | g.55174785_55174810delinsCC | CA645561539 | EGFR | c.2089_2114delinsCC (p.Ala697_Glu705delinsPro) c.597_622delinsCC c.2248_2273delinsCC (p.Ala750_Glu758delinsPro) c.*28+1857_*28+1882delinsCC (n.*28+1857_*28+1882delinsCC) c.2113_2138delinsCC (p.Ala705_Glu713delinsPro) c.1447_1472delinsCC (p.Ala483_Glu491delinsPro) | COSMIC |
7 | g.55174785_55174813delinsCCAAC | CA645561538 | EGFR | c.2089_2117delinsCCAAC (p.Ala697_Ile706delinsProThr) c.597_625delinsCCAAC c.2248_2276delinsCCAAC (p.Ala750_Ile759delinsProThr) c.*28+1857_*28+1885delinsCCAAC (n.*28+1857_*28+1885delinsCCAAC) c.2113_2141delinsCCAAC (p.Ala705_Ile714delinsProThr) c.1447_1475delinsCCAAC (p.Ala483_Ile492delinsProThr) | COSMIC |
7 | g.55174786C>A | CA367584175 | EGFR | c.2090C>A (p.Ala697Glu) c.598C>A c.2249C>A (p.Ala750Glu) c.*28+1858C>A (n.*28+1858C>A) c.2114C>A (p.Ala705Glu) c.1448C>A (p.Ala483Glu) | |
7 | g.55174786C= | CA1708918352 | EGFR | c.2090C= (p.Ala697=) c.598C= c.2249C= (p.Ala750=) c.*28+1858C= (n.*28+1858C=) c.2114C= (p.Ala705=) c.1448C= (p.Ala483=) | |
7 | g.55174786C>G | CA367584176 | EGFR | c.2090C>G (p.Ala697Gly) c.598C>G c.2249C>G (p.Ala750Gly) c.*28+1858C>G (n.*28+1858C>G) c.2114C>G (p.Ala705Gly) c.1448C>G (p.Ala483Gly) | dbSNP |
7 | g.55174786C>T | CA367584177 | EGFR | c.2090C>T (p.Ala697Val) c.598C>T c.2249C>T (p.Ala750Val) c.*28+1858C>T (n.*28+1858C>T) c.2114C>T (p.Ala705Val) c.1448C>T (p.Ala483Val) | ClinVar dbSNP |
7 | g.55174791_55174806del | CA574335579 | EGFR | c.2095_2110del (p.Ser699ArgfsTer9) c.603_618del c.2254_2269del (p.Ser752ArgfsTer9) c.*28+1863_*28+1878del (n.*28+1863_*28+1878del) c.2119_2134del (p.Ser707ArgfsTer9) c.1453_1468del (p.Ser485ArgfsTer9) | dbSNP gnomAD v2 gnomAD v4 |
7 | g.55174786_55174811delinsCAACATCTCCGAAAGCCAACAAGGAA | CA1708918353 | EGFR | c.2090_2115delinsCAACATCTCCGAAAGCCAACAAGGAA (p.Ala697=) c.598_623delinsCAACATCTCCGAAAGCCAACAAGGAA c.2249_2274delinsCAACATCTCCGAAAGCCAACAAGGAA (p.Ala750=) c.*28+1858_*28+1883delinsCAACATCTCCGAAAGCCAACAAGGAA (n.*28+1858_*28+1883delinsCAACATCTCCGAAAGCCAACAAGGAA) c.2114_2139delinsCAACATCTCCGAAAGCCAACAAGGAA (p.Ala705=) c.1448_1473delinsCAACATCTCCGAAAGCCAACAAGGAA (p.Ala483=) | |
7 | g.55174786_55174814delinsGAAGT | CA645561540 | EGFR | c.2090_2118delinsGAAGT (p.Ala697_Ile706delinsGlySer) c.598_626delinsGAAGT c.2249_2277delinsGAAGT (p.Ala750_Ile759delinsGlySer) c.*28+1858_*28+1886delinsGAAGT (n.*28+1858_*28+1886delinsGAAGT) c.2114_2142delinsGAAGT (p.Ala705_Ile714delinsGlySer) c.1448_1476delinsGAAGT (p.Ala483_Ile492delinsGlySer) | COSMIC |
7 | g.55174787A>C | CA454979546 | EGFR | c.2091A>C (p.Ala697=) c.599A>C c.2250A>C (p.Ala750=) c.*28+1859A>C (n.*28+1859A>C) c.2115A>C (p.Ala705=) c.1449A>C (p.Ala483=) | ClinVar |
7 | g.55174787A>G | CA454979549 | EGFR | c.2091A>G (p.Ala697=) c.599A>G c.2250A>G (p.Ala750=) c.*28+1859A>G (n.*28+1859A>G) c.2115A>G (p.Ala705=) c.1449A>G (p.Ala483=) | ClinVar dbSNP |
7 | g.55174787A>T | CA454979551 | EGFR | c.2091A>T (p.Ala697=) c.599A>T c.2250A>T (p.Ala750=) c.*28+1859A>T (n.*28+1859A>T) c.2115A>T (p.Ala705=) c.1449A>T (p.Ala483=) | |
7 | g.55174789_55174812del | CA645561543 | EGFR | c.2093_2116del (p.Thr698_Glu705del) c.601_624del c.2252_2275del (p.Thr751_Glu758del) c.*28+1861_*28+1884del (n.*28+1861_*28+1884del) c.2117_2140del (p.Thr706_Glu713del) c.1451_1474del (p.Thr484_Glu491del) | COSMIC COSMIC |
7 | g.55174788_55174812del | CA180628 | EGFR | c.2092_2116del (p.Thr698SerfsTer7) c.600_624del c.2251_2275del (p.Thr751SerfsTer7) c.*28+1860_*28+1884del (n.*28+1860_*28+1884del) c.2116_2140del (p.Thr706SerfsTer7) c.1450_1474del (p.Thr484SerfsTer7) | ClinVar dbSNP |
7 | g.55174787_55174813delinsCAA | CA645561542 | EGFR | c.2091_2117delinsCAA (p.Thr698_Ile706delinsAsn) c.599_625delinsCAA c.2250_2276delinsCAA (p.Thr751_Ile759delinsAsn) c.*28+1859_*28+1885delinsCAA (n.*28+1859_*28+1885delinsCAA) c.2115_2141delinsCAA (p.Thr706_Ile714delinsAsn) c.1449_1475delinsCAA (p.Thr484_Ile492delinsAsn) | COSMIC |
7 | g.55174787_55174814delinsAACATCTCCGAAAGCCAACAAGGAAATC | CA1708918354 | EGFR | c.2091_2118delinsAACATCTCCGAAAGCCAACAAGGAAATC (p.Ala697=) c.599_626delinsAACATCTCCGAAAGCCAACAAGGAAATC c.2250_2277delinsAACATCTCCGAAAGCCAACAAGGAAATC (p.Ala750=) c.*28+1859_*28+1886delinsAACATCTCCGAAAGCCAACAAGGAAATC (n.*28+1859_*28+1886delinsAACATCTCCGAAAGCCAACAAGGAAATC) c.2115_2142delinsAACATCTCCGAAAGCCAACAAGGAAATC (p.Ala705=) c.1449_1476delinsAACATCTCCGAAAGCCAACAAGGAAATC (p.Ala483=) | |
7 | g.55174788A>C | CA367584178 | EGFR | c.2092A>C (p.Thr698Pro) c.600A>C c.2251A>C (p.Thr751Pro) c.*28+1860A>C (n.*28+1860A>C) c.2116A>C (p.Thr706Pro) c.1450A>C (p.Thr484Pro) | dbSNP |
7 | g.55174788A>G | CA367584179 | EGFR | c.2092A>G (p.Thr698Ala) c.600A>G c.2251A>G (p.Thr751Ala) c.*28+1860A>G (n.*28+1860A>G) c.2116A>G (p.Thr706Ala) c.1450A>G (p.Thr484Ala) | |
7 | g.55174788A>T | CA367584180 | EGFR | c.2092A>T (p.Thr698Ser) c.600A>T c.2251A>T (p.Thr751Ser) c.*28+1860A>T (n.*28+1860A>T) c.2116A>T (p.Thr706Ser) c.1450A>T (p.Thr484Ser) | dbSNP |
7 | g.55174789_55174790del | CA891842028 | EGFR | c.2093_2094del (p.Thr698IlefsTer11) c.601_602del c.2252_2253del (p.Thr751IlefsTer11) c.*28+1861_*28+1862del (n.*28+1861_*28+1862del) c.2117_2118del (p.Thr706IlefsTer11) c.1451_1452del (p.Thr484IlefsTer11) | |
7 | g.55174788_55174813delinsTC | CA645561544 | EGFR | c.2092_2117delinsTC (p.Thr698_Ile706delinsSer) c.600_625delinsTC c.2251_2276delinsTC (p.Thr751_Ile759delinsSer) c.*28+1860_*28+1885delinsTC (n.*28+1860_*28+1885delinsTC) c.2116_2141delinsTC (p.Thr706_Ile714delinsSer) c.1450_1475delinsTC (p.Thr484_Ile492delinsSer) | COSMIC |
7 | g.55174788_55174814delinsGAT | CA180978 | EGFR | c.2092_2118delinsGAT (p.Thr698_Ile706delinsAsp) c.600_626delinsGAT c.2251_2277delinsGAT (p.Thr751_Ile759delinsAsp) c.*28+1860_*28+1886delinsGAT (n.*28+1860_*28+1886delinsGAT) c.2116_2142delinsGAT (p.Thr706_Ile714delinsAsp) c.1450_1476delinsGAT (p.Thr484_Ile492delinsAsp) | ClinVar dbSNP |
7 | g.55174788_55174814delinsTCT | CA645561545 | EGFR | c.2092_2118delinsTCT (p.Thr698_Ile706delinsSer) c.600_626delinsTCT c.2251_2277delinsTCT (p.Thr751_Ile759delinsSer) c.*28+1860_*28+1886delinsTCT (n.*28+1860_*28+1886delinsTCT) c.2116_2142delinsTCT (p.Thr706_Ile714delinsSer) c.1450_1476delinsTCT (p.Thr484_Ile492delinsSer) | COSMIC |
7 | g.55174788_55174814delinsACATCTCCGAAAGCCAACAAGGAAATC | CA1708918355 | EGFR | c.2092_2118delinsACATCTCCGAAAGCCAACAAGGAAATC (p.Thr698=) c.600_626delinsACATCTCCGAAAGCCAACAAGGAAATC c.2251_2277delinsACATCTCCGAAAGCCAACAAGGAAATC (p.Thr751=) c.*28+1860_*28+1886delinsACATCTCCGAAAGCCAACAAGGAAATC (n.*28+1860_*28+1886delinsACATCTCCGAAAGCCAACAAGGAAATC) c.2116_2142delinsACATCTCCGAAAGCCAACAAGGAAATC (p.Thr706=) c.1450_1476delinsACATCTCCGAAAGCCAACAAGGAAATC (p.Thr484=) | |
7 | g.55174789C>A | CA367584182 | EGFR | c.2093C>A (p.Thr698Lys) c.601C>A c.2252C>A (p.Thr751Lys) c.*28+1861C>A (n.*28+1861C>A) c.2117C>A (p.Thr706Lys) c.1451C>A (p.Thr484Lys) | |
7 | g.55174789C= | CA1708918357 | EGFR | c.2093C= (p.Thr698=) c.601C= c.2252C= (p.Thr751=) c.*28+1861C= (n.*28+1861C=) c.2117C= (p.Thr706=) c.1451C= (p.Thr484=) | |
7 | g.55174789C>G | CA367584181 | EGFR | c.2093C>G (p.Thr698Arg) c.601C>G c.2252C>G (p.Thr751Arg) c.*28+1861C>G (n.*28+1861C>G) c.2117C>G (p.Thr706Arg) c.1451C>G (p.Thr484Arg) | |
7 | g.55174789C>T | CA180736 | EGFR | c.2093C>T (p.Thr698Ile) c.601C>T c.2252C>T (p.Thr751Ile) c.*28+1861C>T (n.*28+1861C>T) c.2117C>T (p.Thr706Ile) c.1451C>T (p.Thr484Ile) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC |
7 | g.55174790_55174794del | CA891842029 | EGFR | c.2094_2098del (p.Ser699GlufsTer9) c.602_606del c.2253_2257del (p.Ser752GlufsTer9) c.*28+1862_*28+1866del (n.*28+1862_*28+1866del) c.2118_2122del (p.Ser707GlufsTer9) c.1452_1456del (p.Ser485GlufsTer9) | |
7 | g.55174790_55174801del | CA891842030 | EGFR | c.2094_2105del (p.Ser699_Ala702del) c.602_613del c.2253_2264del (p.Ser752_Ala755del) c.*28+1862_*28+1873del (n.*28+1862_*28+1873del) c.2118_2129del (p.Ser707_Ala710del) c.1452_1463del (p.Ser485_Ala488del) | |
7 | g.55174789_55174812delinsG | CA645561548 | EGFR | c.2093_2116delinsG (p.Thr698SerfsTer4) c.601_624delinsG c.2252_2275delinsG (p.Thr751SerfsTer4) c.*28+1861_*28+1884delinsG (n.*28+1861_*28+1884delinsG) c.2117_2140delinsG (p.Thr706SerfsTer4) c.1451_1474delinsG (p.Thr484SerfsTer4) | COSMIC |
7 | g.55174789_55174813delinsA | CA645561546 | EGFR | c.2093_2117delinsA (p.Thr698_Ile706delinsAsn) c.601_625delinsA c.2252_2276delinsA (p.Thr751_Ile759delinsAsn) c.*28+1861_*28+1885delinsA (n.*28+1861_*28+1885delinsA) c.2117_2141delinsA (p.Thr706_Ile714delinsAsn) c.1451_1475delinsA (p.Thr484_Ile492delinsAsn) | COSMIC |
7 | g.55174789_55174813delinsG | CA645561549 | EGFR | c.2093_2117delinsG (p.Thr698_Ile706delinsSer) c.601_625delinsG c.2252_2276delinsG (p.Thr751_Ile759delinsSer) c.*28+1861_*28+1885delinsG (n.*28+1861_*28+1885delinsG) c.2117_2141delinsG (p.Thr706_Ile714delinsSer) c.1451_1475delinsG (p.Thr484_Ile492delinsSer) | COSMIC |
7 | g.55174789_55174813delinsCATCTCCGAAAGCCAACAAGGAAAT | CA1708918356 | EGFR | c.2093_2117delinsCATCTCCGAAAGCCAACAAGGAAAT (p.Thr698=) c.601_625delinsCATCTCCGAAAGCCAACAAGGAAAT c.2252_2276delinsCATCTCCGAAAGCCAACAAGGAAAT (p.Thr751=) c.*28+1861_*28+1885delinsCATCTCCGAAAGCCAACAAGGAAAT (n.*28+1861_*28+1885delinsCATCTCCGAAAGCCAACAAGGAAAT) c.2117_2141delinsCATCTCCGAAAGCCAACAAGGAAAT (p.Thr706=) c.1451_1475delinsCATCTCCGAAAGCCAACAAGGAAAT (p.Thr484=) | |
7 | g.55174789_55174814delinsAA | CA135815 | EGFR | c.2093_2118delinsAA (p.Thr698_Ile706delinsLys) c.601_626delinsAA c.2252_2277delinsAA (p.Thr751_Ile759delinsLys) c.*28+1861_*28+1886delinsAA (n.*28+1861_*28+1886delinsAA) c.2117_2142delinsAA (p.Thr706_Ile714delinsLys) c.1451_1476delinsAA (p.Thr484_Ile492delinsLys) | ClinVar dbSNP |
7 | g.55174789_55174814delinsAT | CA645561550 | EGFR | c.2093_2118delinsAT (p.Thr698_Ile706delinsAsn) c.601_626delinsAT c.2252_2277delinsAT (p.Thr751_Ile759delinsAsn) c.*28+1861_*28+1886delinsAT (n.*28+1861_*28+1886delinsAT) c.2117_2142delinsAT (p.Thr706_Ile714delinsAsn) c.1451_1476delinsAT (p.Thr484_Ile492delinsAsn) | ClinVar COSMIC |
7 | g.55174789_55174814delinsGAGAAGCG | CA645561547 | EGFR | c.2093_2118delinsGAGAAGCG (p.Thr698_Ile706delinsArgGluAla) c.601_626delinsGAGAAGCG c.2252_2277delinsGAGAAGCG (p.Thr751_Ile759delinsArgGluAla) c.*28+1861_*28+1886delinsGAGAAGCG (n.*28+1861_*28+1886delinsGAGAAGCG) c.2117_2142delinsGAGAAGCG (p.Thr706_Ile714delinsArgGluAla) c.1451_1476delinsGAGAAGCG (p.Thr484_Ile492delinsArgGluAla) | COSMIC |
7 | g.55174789_55174790insCACACGGACTTTATAACAGGCTTTACAAGCTTGAG | CA2775498838 | EGFR | c.2093_2094insCACACGGACTTTATAACAGGCTTTACAAGCTTGAG (p.Ser699ThrfsTer5) c.601_602insCACACGGACTTTATAACAGGCTTTACAAGCTTGAG c.2252_2253insCACACGGACTTTATAACAGGCTTTACAAGCTTGAG (p.Ser752ThrfsTer5) c.*28+1861_*28+1862insCACACGGACTTTATAACAGGCTTTACAAGCTTGAG (n.*28+1861_*28+1862insCACACGGACTTTATAACAGGCTTTACAAGCTTGAG) c.2117_2118insCACACGGACTTTATAACAGGCTTTACAAGCTTGAG (p.Ser707ThrfsTer5) c.1451_1452insCACACGGACTTTATAACAGGCTTTACAAGCTTGAG (p.Ser485ThrfsTer5) | |
7 | g.55174790A>C | CA454979562 | EGFR | c.2094A>C (p.Thr698=) c.602A>C c.2253A>C (p.Thr751=) c.*28+1862A>C (n.*28+1862A>C) c.2118A>C (p.Thr706=) c.1452A>C (p.Thr484=) | dbSNP |
7 | g.55174790A>G | CA454979564 | EGFR | c.2094A>G (p.Thr698=) c.602A>G c.2253A>G (p.Thr751=) c.*28+1862A>G (n.*28+1862A>G) c.2118A>G (p.Thr706=) c.1452A>G (p.Thr484=) | dbSNP |
7 | g.55174790A>T | CA454979565 | EGFR | c.2094A>T (p.Thr698=) c.602A>T c.2253A>T (p.Thr751=) c.*28+1862A>T (n.*28+1862A>T) c.2118A>T (p.Thr706=) c.1452A>T (p.Thr484=) | |
7 | g.55174791_55174798del | CA891842031 | EGFR | c.2095_2102del (p.Pro700GlnfsTer7) c.603_610del c.2254_2261del (p.Pro753GlnfsTer7) c.*28+1863_*28+1870del (n.*28+1863_*28+1870del) c.2119_2126del (p.Pro708GlnfsTer7) c.1453_1460del (p.Pro486GlnfsTer7) | |
7 | g.55174790_55174813del | CA180527 | EGFR | c.2094_2117del (p.Ser699_Ile706del) c.602_625del c.2253_2276del (p.Ser752_Ile759del) c.*28+1862_*28+1885del (n.*28+1862_*28+1885del) c.2118_2141del (p.Ser707_Ile714del) c.1452_1475del (p.Ser485_Ile492del) | ClinVar dbSNP COSMIC |
7 | g.55174790_55174814delinsATCTCCGAAAGCCAACAAGGAAATC | CA1708918358 | EGFR | c.2094_2118delinsATCTCCGAAAGCCAACAAGGAAATC (p.Thr698=) c.602_626delinsATCTCCGAAAGCCAACAAGGAAATC c.2253_2277delinsATCTCCGAAAGCCAACAAGGAAATC (p.Thr751=) c.*28+1862_*28+1886delinsATCTCCGAAAGCCAACAAGGAAATC (n.*28+1862_*28+1886delinsATCTCCGAAAGCCAACAAGGAAATC) c.2118_2142delinsATCTCCGAAAGCCAACAAGGAAATC (p.Thr706=) c.1452_1476delinsATCTCCGAAAGCCAACAAGGAAATC (p.Thr484=) | |
7 | g.55174791T>A | CA367584183 | EGFR | c.2095T>A (p.Ser699Thr) c.603T>A c.2254T>A (p.Ser752Thr) c.*28+1863T>A (n.*28+1863T>A) c.2119T>A (p.Ser707Thr) c.1453T>A (p.Ser485Thr) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
7 | g.55174791T>C | CA367584184 | EGFR | c.2095T>C (p.Ser699Pro) c.603T>C c.2254T>C (p.Ser752Pro) c.*28+1863T>C (n.*28+1863T>C) c.2119T>C (p.Ser707Pro) c.1453T>C (p.Ser485Pro) | ClinVar dbSNP COSMIC |
7 | g.55174791T>G | CA367584185 | EGFR | c.2095T>G (p.Ser699Ala) c.603T>G c.2254T>G (p.Ser752Ala) c.*28+1863T>G (n.*28+1863T>G) c.2119T>G (p.Ser707Ala) c.1453T>G (p.Ser485Ala) | |
7 | g.55174791T= | CA1708918359 | EGFR | c.2095T= (p.Ser699=) c.603T= c.2254T= (p.Ser752=) c.*28+1863T= (n.*28+1863T=) c.2119T= (p.Ser707=) c.1453T= (p.Ser485=) | |
7 | g.55174791_55174792delinsGT | CA2573049003 | EGFR | c.2095_2096delinsGT (p.Ser699Val) c.603_604delinsGT c.2254_2255delinsGT (p.Ser752Val) c.*28+1863_*28+1864delinsGT (n.*28+1863_*28+1864delinsGT) c.2119_2120delinsGT (p.Ser707Val) c.1453_1454delinsGT (p.Ser485Val) | |
7 | g.55174793_55174794del | CA891842033 | EGFR | c.2097_2098del (p.Pro700GlufsTer9) c.605_606del c.2256_2257del (p.Pro753GlufsTer9) c.*28+1865_*28+1866del (n.*28+1865_*28+1866del) c.2121_2122del (p.Pro708GlufsTer9) c.1455_1456del (p.Pro486GlufsTer9) | |
7 | g.55174791_55174814del | CA180524 | EGFR | c.2095_2118del (p.Ser699_Ile706del) c.603_626del c.2254_2277del (p.Ser752_Ile759del) c.*28+1863_*28+1886del (n.*28+1863_*28+1886del) c.2119_2142del (p.Ser707_Ile714del) c.1453_1476del (p.Ser485_Ile492del) | ClinVar dbSNP COSMIC |
7 | g.55174792C>A | CA16602725 | EGFR | c.2096C>A (p.Ser699Tyr) c.604C>A c.2255C>A (p.Ser752Tyr) c.*28+1864C>A (n.*28+1864C>A) c.2120C>A (p.Ser707Tyr) c.1454C>A (p.Ser485Tyr) | ClinVar dbSNP COSMIC |
7 | g.55174792C= | CA1708918360 | EGFR | c.2096C= (p.Ser699=) c.604C= c.2255C= (p.Ser752=) c.*28+1864C= (n.*28+1864C=) c.2120C= (p.Ser707=) c.1454C= (p.Ser485=) | |
7 | g.55174792C>G | CA367584186 | EGFR | c.2096C>G (p.Ser699Cys) c.604C>G c.2255C>G (p.Ser752Cys) c.*28+1864C>G (n.*28+1864C>G) c.2120C>G (p.Ser707Cys) c.1454C>G (p.Ser485Cys) | dbSNP |
7 | g.55174792C>T | CA367584187 | EGFR | c.2096C>T (p.Ser699Phe) c.604C>T c.2255C>T (p.Ser752Phe) c.*28+1864C>T (n.*28+1864C>T) c.2120C>T (p.Ser707Phe) c.1454C>T (p.Ser485Phe) | dbSNP COSMIC |
7 | g.55174793T>A | CA454979578 | EGFR | c.2097T>A (p.Ser699=) c.605T>A c.2256T>A (p.Ser752=) c.*28+1865T>A (n.*28+1865T>A) c.2121T>A (p.Ser707=) c.1455T>A (p.Ser485=) | dbSNP |
7 | g.55174793T>C | CA454979580 | EGFR | c.2097T>C (p.Ser699=) c.605T>C c.2256T>C (p.Ser752=) c.*28+1865T>C (n.*28+1865T>C) c.2121T>C (p.Ser707=) c.1455T>C (p.Ser485=) | |
7 | g.55174793T>G | CA454979577 | EGFR | c.2097T>G (p.Ser699=) c.605T>G c.2256T>G (p.Ser752=) c.*28+1865T>G (n.*28+1865T>G) c.2121T>G (p.Ser707=) c.1455T>G (p.Ser485=) | |
7 | g.55174794C>A | CA367584188 | EGFR | c.2098C>A (p.Pro700Thr) c.606C>A c.2257C>A (p.Pro753Thr) c.*28+1866C>A (n.*28+1866C>A) c.2122C>A (p.Pro708Thr) c.1456C>A (p.Pro486Thr) | dbSNP |
7 | g.55174794C= | CA1708918361 | EGFR | c.2098C= (p.Pro700=) c.606C= c.2257C= (p.Pro753=) c.*28+1866C= (n.*28+1866C=) c.2122C= (p.Pro708=) c.1456C= (p.Pro486=) | |
7 | g.55174794C>G | CA367584189 | EGFR | c.2098C>G (p.Pro700Ala) c.606C>G c.2257C>G (p.Pro753Ala) c.*28+1866C>G (n.*28+1866C>G) c.2122C>G (p.Pro708Ala) c.1456C>G (p.Pro486Ala) | dbSNP |
7 | g.55174794C>T | CA4266020 | EGFR | c.2098C>T (p.Pro700Ser) c.606C>T c.2257C>T (p.Pro753Ser) c.*28+1866C>T (n.*28+1866C>T) c.2122C>T (p.Pro708Ser) c.1456C>T (p.Pro486Ser) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC |
7 | g.55174795_55174815del | CA645561551 | EGFR | c.2099_2119del (p.Pro700_Ile706del) c.607_627del c.2258_2278del (p.Pro753_Ile759del) c.*28+1867_*28+1887del (n.*28+1867_*28+1887del) c.2123_2143del (p.Pro708_Ile714del) c.1457_1477del (p.Pro486_Ile492del) | COSMIC |
7 | g.55174795C>A | CA367584190 | EGFR | c.2099C>A (p.Pro700Gln) c.607C>A c.2258C>A (p.Pro753Gln) c.*28+1867C>A (n.*28+1867C>A) c.2123C>A (p.Pro708Gln) c.1457C>A (p.Pro486Gln) | dbSNP |
7 | g.55174795C= | CA1708918362 | EGFR | c.2099C= (p.Pro700=) c.607C= c.2258C= (p.Pro753=) c.*28+1867C= (n.*28+1867C=) c.2123C= (p.Pro708=) c.1457C= (p.Pro486=) | |
7 | g.55174795C>G | CA367584191 | EGFR | c.2099C>G (p.Pro700Arg) c.607C>G c.2258C>G (p.Pro753Arg) c.*28+1867C>G (n.*28+1867C>G) c.2123C>G (p.Pro708Arg) c.1457C>G (p.Pro486Arg) | dbSNP |
7 | g.55174795C>T | CA4266021 | EGFR | c.2099C>T (p.Pro700Leu) c.607C>T c.2258C>T (p.Pro753Leu) c.*28+1867C>T (n.*28+1867C>T) c.2123C>T (p.Pro708Leu) c.1457C>T (p.Pro486Leu) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
7 | g.55174796G>A | CA4266022 | EGFR | c.2100G>A (p.Pro700=) c.608G>A c.2259G>A (p.Pro753=) c.*28+1868G>A (n.*28+1868G>A) c.2124G>A (p.Pro708=) c.1458G>A (p.Pro486=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
7 | g.55174796G>C | CA454979590 | EGFR | c.2100G>C (p.Pro700=) c.608G>C c.2259G>C (p.Pro753=) c.*28+1868G>C (n.*28+1868G>C) c.2124G>C (p.Pro708=) c.1458G>C (p.Pro486=) | dbSNP |
7 | g.55174796G= | CA1708918363 | EGFR | c.2100G= (p.Pro700=) c.608G= c.2259G= (p.Pro753=) c.*28+1868G= (n.*28+1868G=) c.2124G= (p.Pro708=) c.1458G= (p.Pro486=) | |
7 | g.55174796G>T | CA454979592 | EGFR | c.2100G>T (p.Pro700=) c.608G>T c.2259G>T (p.Pro753=) c.*28+1868G>T (n.*28+1868G>T) c.2124G>T (p.Pro708=) c.1458G>T (p.Pro486=) | dbSNP gnomAD v4 COSMIC |
7 | g.55174797A= | CA1708918364 | EGFR | c.2101A= (p.Lys701=) c.609A= c.2260A= (p.Lys754=) c.*28+1869A= (n.*28+1869A=) c.2125A= (p.Lys709=) c.1459A= (p.Lys487=) | |
7 | g.55174797A>C | CA367584192 | EGFR | c.2101A>C (p.Lys701Gln) c.609A>C c.2260A>C (p.Lys754Gln) c.*28+1869A>C (n.*28+1869A>C) c.2125A>C (p.Lys709Gln) c.1459A>C (p.Lys487Gln) | |
7 | g.55174797A>G | CA135818 | EGFR | c.2101A>G (p.Lys701Glu) c.609A>G c.2260A>G (p.Lys754Glu) c.*28+1869A>G (n.*28+1869A>G) c.2125A>G (p.Lys709Glu) c.1459A>G (p.Lys487Glu) | ClinVar dbSNP COSMIC |
7 | g.55174797A>T | CA367584193 | EGFR | c.2101A>T (p.Lys701Ter) c.609A>T c.2260A>T (p.Lys754Ter) c.*28+1869A>T (n.*28+1869A>T) c.2125A>T (p.Lys709Ter) c.1459A>T (p.Lys487Ter) | |
7 | g.55174797_55174798delinsGC | CA645561552 | EGFR | c.2101_2102delinsGC (p.Lys701Ala) c.609_610delinsGC c.2260_2261delinsGC (p.Lys754Ala) c.*28+1869_*28+1870delinsGC (n.*28+1869_*28+1870delinsGC) c.2125_2126delinsGC (p.Lys709Ala) c.1459_1460delinsGC (p.Lys487Ala) | COSMIC |
7 | g.55174798A>C | CA367584194 | EGFR | c.2102A>C (p.Lys701Thr) c.610A>C c.2261A>C (p.Lys754Thr) c.*28+1870A>C (n.*28+1870A>C) c.2126A>C (p.Lys709Thr) c.1460A>C (p.Lys487Thr) | |
7 | g.55174798A>G | CA367584195 | EGFR | c.2102A>G (p.Lys701Arg) c.610A>G c.2261A>G (p.Lys754Arg) c.*28+1870A>G (n.*28+1870A>G) c.2126A>G (p.Lys709Arg) c.1460A>G (p.Lys487Arg) | COSMIC |
7 | g.55174798A>T | CA367584196 | EGFR | c.2102A>T (p.Lys701Ile) c.610A>T c.2261A>T (p.Lys754Ile) c.*28+1870A>T (n.*28+1870A>T) c.2126A>T (p.Lys709Ile) c.1460A>T (p.Lys487Ile) | dbSNP COSMIC |
7 | g.55174799A>C | CA367584197 | EGFR | c.2103A>C (p.Lys701Asn) c.611A>C c.2262A>C (p.Lys754Asn) c.*28+1871A>C (n.*28+1871A>C) c.2127A>C (p.Lys709Asn) c.1461A>C (p.Lys487Asn) | |
7 | g.55174799A>G | CA454979603 | EGFR | c.2103A>G (p.Lys701=) c.611A>G c.2262A>G (p.Lys754=) c.*28+1871A>G (n.*28+1871A>G) c.2127A>G (p.Lys709=) c.1461A>G (p.Lys487=) | dbSNP COSMIC |
7 | g.55174799A>T | CA367584198 | EGFR | c.2103A>T (p.Lys701Asn) c.611A>T c.2262A>T (p.Lys754Asn) c.*28+1871A>T (n.*28+1871A>T) c.2127A>T (p.Lys709Asn) c.1461A>T (p.Lys487Asn) | |
7 | g.55174800G>A | CA367584199 | EGFR | c.2104G>A (p.Ala702Thr) c.612G>A c.2263G>A (p.Ala755Thr) c.*28+1872G>A (n.*28+1872G>A) c.2128G>A (p.Ala710Thr) c.1462G>A (p.Ala488Thr) | dbSNP COSMIC |
7 | g.55174800G>C | CA367584200 | EGFR | c.2104G>C (p.Ala702Pro) c.612G>C c.2263G>C (p.Ala755Pro) c.*28+1872G>C (n.*28+1872G>C) c.2128G>C (p.Ala710Pro) c.1462G>C (p.Ala488Pro) | dbSNP |
7 | g.55174800G>T | CA367584201 | EGFR | c.2104G>T (p.Ala702Ser) c.612G>T c.2263G>T (p.Ala755Ser) c.*28+1872G>T (n.*28+1872G>T) c.2128G>T (p.Ala710Ser) c.1462G>T (p.Ala488Ser) | dbSNP |
7 | g.55174801C>A | CA367584202 | EGFR | c.2105C>A (p.Ala702Asp) c.613C>A c.2264C>A (p.Ala755Asp) c.*28+1873C>A (n.*28+1873C>A) c.2129C>A (p.Ala710Asp) c.1463C>A (p.Ala488Asp) | dbSNP |
7 | g.55174801C>G | CA367584204 | EGFR | c.2105C>G (p.Ala702Gly) c.613C>G c.2264C>G (p.Ala755Gly) c.*28+1873C>G (n.*28+1873C>G) c.2129C>G (p.Ala710Gly) c.1463C>G (p.Ala488Gly) | dbSNP |
7 | g.55174801C>T | CA367584203 | EGFR | c.2105C>T (p.Ala702Val) c.613C>T c.2264C>T (p.Ala755Val) c.*28+1873C>T (n.*28+1873C>T) c.2129C>T (p.Ala710Val) c.1463C>T (p.Ala488Val) | dbSNP COSMIC |
7 | g.55174802C>A | CA454979611 | EGFR | c.2106C>A (p.Ala702=) c.614C>A c.2265C>A (p.Ala755=) c.*28+1874C>A (n.*28+1874C>A) c.2130C>A (p.Ala710=) c.1464C>A (p.Ala488=) | dbSNP |
7 | g.55174802C= | CA1708918365 | EGFR | c.2106C= (p.Ala702=) c.614C= c.2265C= (p.Ala755=) c.*28+1874C= (n.*28+1874C=) c.2130C= (p.Ala710=) c.1464C= (p.Ala488=) | |
7 | g.55174802C>G | CA176003 | EGFR | c.2106C>G (p.Ala702=) c.614C>G c.2265C>G (p.Ala755=) c.*28+1874C>G (n.*28+1874C>G) c.2130C>G (p.Ala710=) c.1464C>G (p.Ala488=) | ClinVar dbSNP |
7 | g.55174802C>T | CA454979613 | EGFR | c.2106C>T (p.Ala702=) c.614C>T c.2265C>T (p.Ala755=) c.*28+1874C>T (n.*28+1874C>T) c.2130C>T (p.Ala710=) c.1464C>T (p.Ala488=) | dbSNP COSMIC |
7 | g.55174805_55174807dup | CA645561553 | EGFR | c.2109_2111dup (p.Asn703_Lys704insAsn) c.617_619dup c.2268_2270dup (p.Asn756_Lys757insAsn) c.*28+1877_*28+1879dup (n.*28+1877_*28+1879dup) c.2133_2135dup (p.Asn711_Lys712insAsn) c.1467_1469dup (p.Asn489_Lys490insAsn) | COSMIC |
7 | g.55174803A>C | CA367584205 | EGFR | c.2107A>C (p.Asn703His) c.615A>C c.2266A>C (p.Asn756His) c.*28+1875A>C (n.*28+1875A>C) c.2131A>C (p.Asn711His) c.1465A>C (p.Asn489His) | |
7 | g.55174803A>G | CA367584206 | EGFR | c.2107A>G (p.Asn703Asp) c.615A>G c.2266A>G (p.Asn756Asp) c.*28+1875A>G (n.*28+1875A>G) c.2131A>G (p.Asn711Asp) c.1465A>G (p.Asn489Asp) | |
7 | g.55174803A>T | CA367584207 | EGFR | c.2107A>T (p.Asn703Tyr) c.615A>T c.2266A>T (p.Asn756Tyr) c.*28+1875A>T (n.*28+1875A>T) c.2131A>T (p.Asn711Tyr) c.1465A>T (p.Asn489Tyr) | dbSNP COSMIC |
7 | g.55174804A= | CA1708918366 | EGFR | c.2108A= (p.Asn703=) c.616A= c.2267A= (p.Asn756=) c.*28+1876A= (n.*28+1876A=) c.2132A= (p.Asn711=) c.1466A= (p.Asn489=) | |
7 | g.55174804A>C | CA367584210 | EGFR | c.2108A>C (p.Asn703Thr) c.616A>C c.2267A>C (p.Asn756Thr) c.*28+1876A>C (n.*28+1876A>C) c.2132A>C (p.Asn711Thr) c.1466A>C (p.Asn489Thr) | dbSNP |
7 | g.55174804A>G | CA367584208 | EGFR | c.2108A>G (p.Asn703Ser) c.616A>G c.2267A>G (p.Asn756Ser) c.*28+1876A>G (n.*28+1876A>G) c.2132A>G (p.Asn711Ser) c.1466A>G (p.Asn489Ser) | ClinVar dbSNP gnomAD v4 COSMIC |
7 | g.55174804A>T | CA367584209 | EGFR | c.2108A>T (p.Asn703Ile) c.616A>T c.2267A>T (p.Asn756Ile) c.*28+1876A>T (n.*28+1876A>T) c.2132A>T (p.Asn711Ile) c.1466A>T (p.Asn489Ile) | dbSNP |
7 | g.55174805C>A | CA367584211 | EGFR | c.2109C>A (p.Asn703Lys) c.617C>A c.2268C>A (p.Asn756Lys) c.*28+1877C>A (n.*28+1877C>A) c.2133C>A (p.Asn711Lys) c.1467C>A (p.Asn489Lys) | dbSNP |
7 | g.55174805C= | CA1708918367 | EGFR | c.2109C= (p.Asn703=) c.617C= c.2268C= (p.Asn756=) c.*28+1877C= (n.*28+1877C=) c.2133C= (p.Asn711=) c.1467C= (p.Asn489=) | |
7 | g.55174805C>G | CA367584212 | EGFR | c.2109C>G (p.Asn703Lys) c.617C>G c.2268C>G (p.Asn756Lys) c.*28+1877C>G (n.*28+1877C>G) c.2133C>G (p.Asn711Lys) c.1467C>G (p.Asn489Lys) | dbSNP |
7 | g.55174805C>T | CA454979623 | EGFR | c.2109C>T (p.Asn703=) c.617C>T c.2268C>T (p.Asn756=) c.*28+1877C>T (n.*28+1877C>T) c.2133C>T (p.Asn711=) c.1467C>T (p.Asn489=) | dbSNP gnomAD v2 gnomAD v4 |
7 | g.55174806A>C | CA367584213 | EGFR | c.2110A>C (p.Lys704Gln) c.618A>C c.2269A>C (p.Lys757Gln) c.*28+1878A>C (n.*28+1878A>C) c.2134A>C (p.Lys712Gln) c.1468A>C (p.Lys490Gln) | |
7 | g.55174806A>G | CA367584214 | EGFR | c.2110A>G (p.Lys704Glu) c.618A>G c.2269A>G (p.Lys757Glu) c.*28+1878A>G (n.*28+1878A>G) c.2134A>G (p.Lys712Glu) c.1468A>G (p.Lys490Glu) | dbSNP |
7 | g.55174806A>T | CA367584215 | EGFR | c.2110A>T (p.Lys704Ter) c.618A>T c.2269A>T (p.Lys757Ter) c.*28+1878A>T (n.*28+1878A>T) c.2134A>T (p.Lys712Ter) c.1468A>T (p.Lys490Ter) | dbSNP |
7 | g.55174807A= | CA1708918368 | EGFR | c.2111A= (p.Lys704=) c.619A= c.2270A= (p.Lys757=) c.*28+1879A= (n.*28+1879A=) c.2135A= (p.Lys712=) c.1469A= (p.Lys490=) | |
7 | g.55174807A>C | CA367584216 | EGFR | c.2111A>C (p.Lys704Thr) c.619A>C c.2270A>C (p.Lys757Thr) c.*28+1879A>C (n.*28+1879A>C) c.2135A>C (p.Lys712Thr) c.1469A>C (p.Lys490Thr) | |
7 | g.55174807A>G | CA4266023 | EGFR | c.2111A>G (p.Lys704Arg) c.619A>G c.2270A>G (p.Lys757Arg) c.*28+1879A>G (n.*28+1879A>G) c.2135A>G (p.Lys712Arg) c.1469A>G (p.Lys490Arg) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC |
7 | g.55174807A>T | CA135821 | EGFR | c.2111A>T (p.Lys704Met) c.619A>T c.2270A>T (p.Lys757Met) c.*28+1879A>T (n.*28+1879A>T) c.2135A>T (p.Lys712Met) c.1469A>T (p.Lys490Met) | ClinVar dbSNP COSMIC |
7 | g.55174808G>A | CA454979634 | EGFR | c.2112G>A (p.Lys704=) c.620G>A c.2271G>A (p.Lys757=) c.*28+1880G>A (n.*28+1880G>A) c.2136G>A (p.Lys712=) c.1470G>A (p.Lys490=) | ClinVar dbSNP |
7 | g.55174808G>C | CA367584217 | EGFR | c.2112G>C (p.Lys704Asn) c.620G>C c.2271G>C (p.Lys757Asn) c.*28+1880G>C (n.*28+1880G>C) c.2136G>C (p.Lys712Asn) c.1470G>C (p.Lys490Asn) | dbSNP |
7 | g.55174808G= | CA1708918369 | EGFR | c.2112G= (p.Lys704=) c.620G= c.2271G= (p.Lys757=) c.*28+1880G= (n.*28+1880G=) c.2136G= (p.Lys712=) c.1470G= (p.Lys490=) | |
7 | g.55174808G>T | CA367584218 | EGFR | c.2112G>T (p.Lys704Asn) c.620G>T c.2271G>T (p.Lys757Asn) c.*28+1880G>T (n.*28+1880G>T) c.2136G>T (p.Lys712Asn) c.1470G>T (p.Lys490Asn) | dbSNP |
7 | g.55174809G>A | CA367584219 | EGFR | c.2113G>A (p.Glu705Lys) c.621G>A c.2272G>A (p.Glu758Lys) c.*28+1881G>A (n.*28+1881G>A) c.2137G>A (p.Glu713Lys) c.1471G>A (p.Glu491Lys) | dbSNP gnomAD v4 COSMIC |
7 | g.55174809G>C | CA367584220 | EGFR | c.2113G>C (p.Glu705Gln) c.621G>C c.2272G>C (p.Glu758Gln) c.*28+1881G>C (n.*28+1881G>C) c.2137G>C (p.Glu713Gln) c.1471G>C (p.Glu491Gln) | dbSNP gnomAD v4 |
7 | g.55174809G= | CA1708918370 | EGFR | c.2113G= (p.Glu705=) c.621G= c.2272G= (p.Glu758=) c.*28+1881G= (n.*28+1881G=) c.2137G= (p.Glu713=) c.1471G= (p.Glu491=) | |
7 | g.55174809G>T | CA367584221 | EGFR | c.2113G>T (p.Glu705Ter) c.621G>T c.2272G>T (p.Glu758Ter) c.*28+1881G>T (n.*28+1881G>T) c.2137G>T (p.Glu713Ter) c.1471G>T (p.Glu491Ter) | |
7 | g.55174810A= | CA1708918371 | EGFR | c.2114A= (p.Glu705=) c.622A= c.2273A= (p.Glu758=) c.*28+1882A= (n.*28+1882A=) c.2138A= (p.Glu713=) c.1472A= (p.Glu491=) | |
7 | g.55174810A>C | CA367584222 | EGFR | c.2114A>C (p.Glu705Ala) c.622A>C c.2273A>C (p.Glu758Ala) c.*28+1882A>C (n.*28+1882A>C) c.2138A>C (p.Glu713Ala) c.1472A>C (p.Glu491Ala) | |
7 | g.55174810A>G | CA4266024 | EGFR | c.2114A>G (p.Glu705Gly) c.622A>G c.2273A>G (p.Glu758Gly) c.*28+1882A>G (n.*28+1882A>G) c.2138A>G (p.Glu713Gly) c.1472A>G (p.Glu491Gly) | dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC |
7 | g.55174810A>T | CA367584223 | EGFR | c.2114A>T (p.Glu705Val) c.622A>T c.2273A>T (p.Glu758Val) c.*28+1882A>T (n.*28+1882A>T) c.2138A>T (p.Glu713Val) c.1472A>T (p.Glu491Val) | |
7 | g.55174811A>C | CA367584224 | EGFR | c.2115A>C (p.Glu705Asp) c.623A>C c.2274A>C (p.Glu758Asp) c.*28+1883A>C (n.*28+1883A>C) c.2139A>C (p.Glu713Asp) c.1473A>C (p.Glu491Asp) | dbSNP COSMIC |
7 | g.55174811A>G | CA454979645 | EGFR | c.2115A>G (p.Glu705=) c.623A>G c.2274A>G (p.Glu758=) c.*28+1883A>G (n.*28+1883A>G) c.2139A>G (p.Glu713=) c.1473A>G (p.Glu491=) | gnomAD v4 |
7 | g.55174811A>T | CA367584225 | EGFR | c.2115A>T (p.Glu705Asp) c.623A>T c.2274A>T (p.Glu758Asp) c.*28+1883A>T (n.*28+1883A>T) c.2139A>T (p.Glu713Asp) c.1473A>T (p.Glu491Asp) | ClinVar dbSNP |
7 | g.55174812A>C | CA367584226 | EGFR | c.2116A>C (p.Ile706Leu) c.624A>C c.2275A>C (p.Ile759Leu) c.*28+1884A>C (n.*28+1884A>C) c.2140A>C (p.Ile714Leu) c.1474A>C (p.Ile492Leu) | dbSNP |
7 | g.55174812A>G | CA367584227 | EGFR | c.2116A>G (p.Ile706Val) c.624A>G c.2275A>G (p.Ile759Val) c.*28+1884A>G (n.*28+1884A>G) c.2140A>G (p.Ile714Val) c.1474A>G (p.Ile492Val) | dbSNP gnomAD v4 |
7 | g.55174812A>T | CA367584228 | EGFR | c.2116A>T (p.Ile706Phe) c.624A>T c.2275A>T (p.Ile759Phe) c.*28+1884A>T (n.*28+1884A>T) c.2140A>T (p.Ile714Phe) c.1474A>T (p.Ile492Phe) | dbSNP |
7 | g.55174813T>A | CA367584229 | EGFR | c.2117T>A (p.Ile706Asn) c.625T>A c.2276T>A (p.Ile759Asn) c.*28+1885T>A (n.*28+1885T>A) c.2141T>A (p.Ile714Asn) c.1475T>A (p.Ile492Asn) | ClinVar dbSNP COSMIC |
7 | g.55174813T>C | CA367584230 | EGFR | c.2117T>C (p.Ile706Thr) c.625T>C c.2276T>C (p.Ile759Thr) c.*28+1885T>C (n.*28+1885T>C) c.2141T>C (p.Ile714Thr) c.1475T>C (p.Ile492Thr) | |
7 | g.55174813T>G | CA367584231 | EGFR | c.2117T>G (p.Ile706Ser) c.625T>G c.2276T>G (p.Ile759Ser) c.*28+1885T>G (n.*28+1885T>G) c.2141T>G (p.Ile714Ser) c.1475T>G (p.Ile492Ser) | |
7 | g.55174813T= | CA1708918372 | EGFR | c.2117T= (p.Ile706=) c.625T= c.2276T= (p.Ile759=) c.*28+1885T= (n.*28+1885T=) c.2141T= (p.Ile714=) c.1475T= (p.Ile492=) | |
7 | g.55174814C>A | CA454979655 | EGFR | c.2118C>A (p.Ile706=) c.626C>A c.2277C>A (p.Ile759=) c.*28+1886C>A (n.*28+1886C>A) c.2142C>A (p.Ile714=) c.1476C>A (p.Ile492=) | dbSNP |
7 | g.55174814C= | CA1708918373 | EGFR | c.2118C= (p.Ile706=) c.626C= c.2277C= (p.Ile759=) c.*28+1886C= (n.*28+1886C=) c.2142C= (p.Ile714=) c.1476C= (p.Ile492=) | |
7 | g.55174814C>G | CA367584232 | EGFR | c.2118C>G (p.Ile706Met) c.626C>G c.2277C>G (p.Ile759Met) c.*28+1886C>G (n.*28+1886C>G) c.2142C>G (p.Ile714Met) c.1476C>G (p.Ile492Met) | ClinVar dbSNP |
7 | g.55174814C>T | CA454979658 | EGFR | c.2118C>T (p.Ile706=) c.626C>T c.2277C>T (p.Ile759=) c.*28+1886C>T (n.*28+1886C>T) c.2142C>T (p.Ile714=) c.1476C>T (p.Ile492=) | dbSNP |
7 | g.55174814_55174815insT | CA176006 | EGFR | c.2118_2119insT (p.Leu707SerfsTer3) c.626_627insT c.2277_2278insT (p.Leu760SerfsTer3) c.*28+1886_*28+1887insT (n.*28+1886_*28+1887insT) c.2142_2143insT (p.Leu715SerfsTer3) c.1476_1477insT (p.Leu493SerfsTer3) | ClinVar dbSNP |
7 | g.55174815C>A | CA367584233 | EGFR | c.2119C>A (p.Leu707Ile) c.627C>A c.2278C>A (p.Leu760Ile) c.*28+1887C>A (n.*28+1887C>A) c.2143C>A (p.Leu715Ile) c.1477C>A (p.Leu493Ile) | dbSNP |
7 | g.55174815C>G | CA367584234 | EGFR | c.2119C>G (p.Leu707Val) c.627C>G c.2278C>G (p.Leu760Val) c.*28+1887C>G (n.*28+1887C>G) c.2143C>G (p.Leu715Val) c.1477C>G (p.Leu493Val) | dbSNP |
7 | g.55174815C>T | CA367584235 | EGFR | c.2119C>T (p.Leu707Phe) c.627C>T c.2278C>T (p.Leu760Phe) c.*28+1887C>T (n.*28+1887C>T) c.2143C>T (p.Leu715Phe) c.1477C>T (p.Leu493Phe) | ClinVar dbSNP gnomAD v4 COSMIC |
7 | g.55174816T>A | CA367584238 | EGFR | c.2120T>A (p.Leu707His) c.628T>A c.2279T>A (p.Leu760His) c.*28+1888T>A (n.*28+1888T>A) c.2144T>A (p.Leu715His) c.1478T>A (p.Leu493His) | dbSNP |
7 | g.55174816T>C | CA367584236 | EGFR | c.2120T>C (p.Leu707Pro) c.628T>C c.2279T>C (p.Leu760Pro) c.*28+1888T>C (n.*28+1888T>C) c.2144T>C (p.Leu715Pro) c.1478T>C (p.Leu493Pro) | dbSNP |
7 | g.55174816T>G | CA367584237 | EGFR | c.2120T>G (p.Leu707Arg) c.628T>G c.2279T>G (p.Leu760Arg) c.*28+1888T>G (n.*28+1888T>G) c.2144T>G (p.Leu715Arg) c.1478T>G (p.Leu493Arg) | |
7 | g.55174817C>A | CA454979669 | EGFR | c.2121C>A (p.Leu707=) c.629C>A c.2280C>A (p.Leu760=) c.*28+1889C>A (n.*28+1889C>A) c.2145C>A (p.Leu715=) c.1479C>A (p.Leu493=) | dbSNP gnomAD v4 |
7 | g.55174817C= | CA1708918374 | EGFR | c.2121C= (p.Leu707=) c.629C= c.2280C= (p.Leu760=) c.*28+1889C= (n.*28+1889C=) c.2145C= (p.Leu715=) c.1479C= (p.Leu493=) | |
7 | g.55174817C>G | CA454979670 | EGFR | c.2121C>G (p.Leu707=) c.629C>G c.2280C>G (p.Leu760=) c.*28+1889C>G (n.*28+1889C>G) c.2145C>G (p.Leu715=) c.1479C>G (p.Leu493=) | ClinVar dbSNP |
7 | g.55174817C>T | CA135824 | EGFR | c.2121C>T (p.Leu707=) c.629C>T c.2280C>T (p.Leu760=) c.*28+1889C>T (n.*28+1889C>T) c.2145C>T (p.Leu715=) c.1479C>T (p.Leu493=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
7 | g.55174818G>A | CA16602543 | EGFR | c.2122G>A (p.Asp708Asn) c.630G>A c.2281G>A (p.Asp761Asn) c.*28+1890G>A (n.*28+1890G>A) c.2146G>A (p.Asp716Asn) c.1480G>A (p.Asp494Asn) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
7 | g.55174818G>C | CA367584239 | EGFR | c.2122G>C (p.Asp708His) c.630G>C c.2281G>C (p.Asp761His) c.*28+1890G>C (n.*28+1890G>C) c.2146G>C (p.Asp716His) c.1480G>C (p.Asp494His) | ClinVar dbSNP gnomAD v4 |
7 | g.55174818G= | CA1708918375 | EGFR | c.2122G= (p.Asp708=) c.630G= c.2281G= (p.Asp761=) c.*28+1890G= (n.*28+1890G=) c.2146G= (p.Asp716=) c.1480G= (p.Asp494=) | |
7 | g.55174818G>T | CA135827 | EGFR | c.2122G>T (p.Asp708Tyr) c.630G>T c.2281G>T (p.Asp761Tyr) c.*28+1890G>T (n.*28+1890G>T) c.2146G>T (p.Asp716Tyr) c.1480G>T (p.Asp494Tyr) | ClinVar dbSNP gnomAD v4 COSMIC |
7 | g.55174819A= | CA1708918376 | EGFR | c.2123A= (p.Asp708=) c.631A= c.2282A= (p.Asp761=) c.*28+1891A= (n.*28+1891A=) c.2147A= (p.Asp716=) c.1481A= (p.Asp494=) | |
7 | g.55174819A>C | CA367584240 | EGFR | c.2123A>C (p.Asp708Ala) c.631A>C c.2282A>C (p.Asp761Ala) c.*28+1891A>C (n.*28+1891A>C) c.2147A>C (p.Asp716Ala) c.1481A>C (p.Asp494Ala) | |
7 | g.55174819A>G | CA367584241 | EGFR | c.2123A>G (p.Asp708Gly) c.631A>G c.2282A>G (p.Asp761Gly) c.*28+1891A>G (n.*28+1891A>G) c.2147A>G (p.Asp716Gly) c.1481A>G (p.Asp494Gly) | ClinVar dbSNP gnomAD v4 COSMIC |
7 | g.55174819A>T | CA367584242 | EGFR | c.2123A>T (p.Asp708Val) c.631A>T c.2282A>T (p.Asp761Val) c.*28+1891A>T (n.*28+1891A>T) c.2147A>T (p.Asp716Val) c.1481A>T (p.Asp494Val) | dbSNP |
7 | g.55174820T>A | CA367584243 | EGFR | c.2124T>A (p.Asp708Glu) c.632T>A c.2283T>A (p.Asp761Glu) c.*28+1892T>A (n.*28+1892T>A) c.2148T>A (p.Asp716Glu) c.1482T>A (p.Asp494Glu) | dbSNP |
7 | g.55174820T>C | CA454979681 | EGFR | c.2124T>C (p.Asp708=) c.632T>C c.2283T>C (p.Asp761=) c.*28+1892T>C (n.*28+1892T>C) c.2148T>C (p.Asp716=) c.1482T>C (p.Asp494=) | gnomAD v4 |
7 | g.55174820T>G | CA367584244 | EGFR | c.2124T>G (p.Asp708Glu) c.632T>G c.2283T>G (p.Asp761Glu) c.*28+1892T>G (n.*28+1892T>G) c.2148T>G (p.Asp716Glu) c.1482T>G (p.Asp494Glu) | |
7 | g.55174821G>A | CA135831 | EGFR | c.2124+1G>A (n.2124+1G>A) c.632+1G>A c.2283+1G>A (n.2283+1G>A) c.*28+1893G>A (n.*28+1893G>A) c.2148+1G>A (n.2148+1G>A) c.1482+1G>A (n.1482+1G>A) | ClinVar dbSNP |
7 | g.55174821G>C | CA367584245 | EGFR | c.2124+1G>C (n.2124+1G>C) c.632+1G>C c.2283+1G>C (n.2283+1G>C) c.*28+1893G>C (n.*28+1893G>C) c.2148+1G>C (n.2148+1G>C) c.1482+1G>C (n.1482+1G>C) | dbSNP |
7 | g.55174821G= | CA1708918377 | EGFR | c.2124+1G= (n.2124+1G=) c.632+1G= c.2283+1G= (n.2283+1G=) c.*28+1893G= (n.*28+1893G=) c.2148+1G= (n.2148+1G=) c.1482+1G= (n.1482+1G=) | |
7 | g.55174821G>T | CA367584246 | EGFR | c.2124+1G>T (n.2124+1G>T) c.632+1G>T c.2283+1G>T (n.2283+1G>T) c.*28+1893G>T (n.*28+1893G>T) c.2148+1G>T (n.2148+1G>T) c.1482+1G>T (n.1482+1G>T) | |
7 | g.55174822T>A | CA367584247 | EGFR | c.2124+2T>A (n.2124+2T>A) c.632+2T>A c.2283+2T>A (n.2283+2T>A) c.*28+1894T>A (n.*28+1894T>A) c.2148+2T>A (n.2148+2T>A) c.1482+2T>A (n.1482+2T>A) | dbSNP |
7 | g.55174822T>C | CA367584249 | EGFR | c.2124+2T>C (n.2124+2T>C) c.632+2T>C c.2283+2T>C (n.2283+2T>C) c.*28+1894T>C (n.*28+1894T>C) c.2148+2T>C (n.2148+2T>C) c.1482+2T>C (n.1482+2T>C) | dbSNP |
7 | g.55174822T>G | CA367584248 | EGFR | c.2124+2T>G (n.2124+2T>G) c.632+2T>G c.2283+2T>G (n.2283+2T>G) c.*28+1894T>G (n.*28+1894T>G) c.2148+2T>G (n.2148+2T>G) c.1482+2T>G (n.1482+2T>G) | gnomAD v4 |
7 | g.55174823G>A | CA2714960544 | EGFR | c.2124+3G>A (n.2124+3G>A) c.632+3G>A c.2283+3G>A (n.2283+3G>A) c.*28+1895G>A (n.*28+1895G>A) c.2148+3G>A (n.2148+3G>A) c.1482+3G>A (n.1482+3G>A) | dbSNP |
7 | g.55174823G>C | CA2714960545 | EGFR | c.2124+3G>C (n.2124+3G>C) c.632+3G>C c.2283+3G>C (n.2283+3G>C) c.*28+1895G>C (n.*28+1895G>C) c.2148+3G>C (n.2148+3G>C) c.1482+3G>C (n.1482+3G>C) | dbSNP |
7 | g.55174824A>G | CA2714960546 | EGFR | c.2124+4A>G (n.2124+4A>G) c.632+4A>G c.2283+4A>G (n.2283+4A>G) c.*28+1896A>G (n.*28+1896A>G) c.2148+4A>G (n.2148+4A>G) c.1482+4A>G (n.1482+4A>G) | dbSNP |
7 | g.55174824A>T | CA2714960549 | EGFR | c.2124+4A>T (n.2124+4A>T) c.632+4A>T c.2283+4A>T (n.2283+4A>T) c.*28+1896A>T (n.*28+1896A>T) c.2148+4A>T (n.2148+4A>T) c.1482+4A>T (n.1482+4A>T) | dbSNP |
7 | g.55174825G>A | CA2714960550 | EGFR | c.2124+5G>A (n.2124+5G>A) c.632+5G>A c.2283+5G>A (n.2283+5G>A) c.*28+1897G>A (n.*28+1897G>A) c.2148+5G>A (n.2148+5G>A) c.1482+5G>A (n.1482+5G>A) | dbSNP |
7 | g.55174825G>C | CA2714960551 | EGFR | c.2124+5G>C (n.2124+5G>C) c.632+5G>C c.2283+5G>C (n.2283+5G>C) c.*28+1897G>C (n.*28+1897G>C) c.2148+5G>C (n.2148+5G>C) c.1482+5G>C (n.1482+5G>C) | dbSNP |
7 | g.55174825G>T | CA2714960552 | EGFR | c.2124+5G>T (n.2124+5G>T) c.632+5G>T c.2283+5G>T (n.2283+5G>T) c.*28+1897G>T (n.*28+1897G>T) c.2148+5G>T (n.2148+5G>T) c.1482+5G>T (n.1482+5G>T) | dbSNP |
7 | g.55174826T>A | CA2714571712 | EGFR | c.2124+6T>A (n.2124+6T>A) c.632+6T>A c.2283+6T>A (n.2283+6T>A) c.*28+1898T>A (n.*28+1898T>A) c.2148+6T>A (n.2148+6T>A) c.1482+6T>A (n.1482+6T>A) | dbSNP |
7 | g.55174826T>C | CA1708918379 | EGFR | c.2124+6T>C (n.2124+6T>C) c.632+6T>C c.2283+6T>C (n.2283+6T>C) c.*28+1898T>C (n.*28+1898T>C) c.2148+6T>C (n.2148+6T>C) c.1482+6T>C (n.1482+6T>C) | dbSNP |
7 | g.55174826T>G | CA2682854898 | EGFR | c.2124+6T>G (n.2124+6T>G) c.632+6T>G c.2283+6T>G (n.2283+6T>G) c.*28+1898T>G (n.*28+1898T>G) c.2148+6T>G (n.2148+6T>G) c.1482+6T>G (n.1482+6T>G) | dbSNP gnomAD v4 |
7 | g.55174826T= | CA1708918378 | EGFR | c.2124+6T= (n.2124+6T=) c.632+6T= c.2283+6T= (n.2283+6T=) c.*28+1898T= (n.*28+1898T=) c.2148+6T= (n.2148+6T=) c.1482+6T= (n.1482+6T=) | |
7 | g.55174827T>A | CA2714960553 | EGFR | c.2124+7T>A (n.2124+7T>A) c.632+7T>A c.2283+7T>A (n.2283+7T>A) c.*28+1899T>A (n.*28+1899T>A) c.2148+7T>A (n.2148+7T>A) c.1482+7T>A (n.1482+7T>A) | dbSNP |
7 | g.55174828T>A | CA2714515514 | EGFR | c.2124+8T>A (n.2124+8T>A) c.632+8T>A c.2283+8T>A (n.2283+8T>A) c.*28+1900T>A (n.*28+1900T>A) c.2148+8T>A (n.2148+8T>A) c.1482+8T>A (n.1482+8T>A) | dbSNP |
7 | g.55174828T>G | CA158932705 | EGFR | c.2124+8T>G (n.2124+8T>G) c.632+8T>G c.2283+8T>G (n.2283+8T>G) c.*28+1900T>G (n.*28+1900T>G) c.2148+8T>G (n.2148+8T>G) c.1482+8T>G (n.1482+8T>G) | ClinVar dbSNP |
7 | g.55174828T= | CA1708918380 | EGFR | c.2124+8T= (n.2124+8T=) c.632+8T= c.2283+8T= (n.2283+8T=) c.*28+1900T= (n.*28+1900T=) c.2148+8T= (n.2148+8T=) c.1482+8T= (n.1482+8T=) | |
7 | g.55174829C>G | CA2714960573 | EGFR | c.2124+9C>G (n.2124+9C>G) c.632+9C>G c.2283+9C>G (n.2283+9C>G) c.*28+1901C>G (n.*28+1901C>G) c.2148+9C>G (n.2148+9C>G) c.1482+9C>G (n.1482+9C>G) | ClinVar dbSNP |
7 | g.55174829C>T | CA2714960574 | EGFR | c.2124+9C>T (n.2124+9C>T) c.632+9C>T c.2283+9C>T (n.2283+9C>T) c.*28+1901C>T (n.*28+1901C>T) c.2148+9C>T (n.2148+9C>T) c.1482+9C>T (n.1482+9C>T) | dbSNP |
7 | g.55174830T>A | CA2714960576 | EGFR | c.2124+10T>A (n.2124+10T>A) c.632+10T>A c.2283+10T>A (n.2283+10T>A) c.*28+1902T>A (n.*28+1902T>A) c.2148+10T>A (n.2148+10T>A) c.1482+10T>A (n.1482+10T>A) | dbSNP |
7 | g.55174830T>C | CA2739265455 | EGFR | c.2124+10T>C (n.2124+10T>C) c.632+10T>C c.2283+10T>C (n.2283+10T>C) c.*28+1902T>C (n.*28+1902T>C) c.2148+10T>C (n.2148+10T>C) c.1482+10T>C (n.1482+10T>C) | ClinVar |
7 | g.55174830T>G | CA2714960577 | EGFR | c.2124+10T>G (n.2124+10T>G) c.632+10T>G c.2283+10T>G (n.2283+10T>G) c.*28+1902T>G (n.*28+1902T>G) c.2148+10T>G (n.2148+10T>G) c.1482+10T>G (n.1482+10T>G) | dbSNP |
7 | g.55174830_55174966delinsTGCTTTGCTGTGTGGGGGTCCATGGCTCTGAACCTCAGGCCCACCTTTTCTCATGTCTGGCAGCTGCTCTGCTCTAGACCCTGCTCATCTCCACATCCTAAATGTTCACTTTCTATGTCTTTCCCTTTCTAGCTCTA | CA1708918381 | EGFR | c.2124+10_2124+146delinsTGCTTTGCTGTGTGGGGGTCCATGGCTCTGAACCTCAGGCCCACCTTTTCTCATGTCTGGCAGCTGCTCTGCTCTAGACCCTGCTCATCTCCACATCCTAAATGTTCACTTTCTATGTCTTTCCCTTTCTAGCTCTA (n.2124+10_2124+146delinsTGCTTTGCTGTGTGGGGGTCCATGGCTCTGAACCTCAGGCCCACCTTTTCTCATGTCTGGCAGCTGCTCTGCTCTAGACCCTGCTCATCTCCACATCCTAAATGTTCACTTTCTATGTCTTTCCCTTTCTAGCTCTA) c.632+10_632+146delinsTGCTTTGCTGTGTGGGGGTCCATGGCTCTGAACCTCAGGCCCACCTTTTCTCATGTCTGGCAGCTGCTCTGCTCTAGACCCTGCTCATCTCCACATCCTAAATGTTCACTTTCTATGTCTTTCCCTTTCTAGCTCTA c.2283+10_2283+146delinsTGCTTTGCTGTGTGGGGGTCCATGGCTCTGAACCTCAGGCCCACCTTTTCTCATGTCTGGCAGCTGCTCTGCTCTAGACCCTGCTCATCTCCACATCCTAAATGTTCACTTTCTATGTCTTTCCCTTTCTAGCTCTA (n.2283+10_2283+146delinsTGCTTTGCTGTGTGGGGGTCCATGGCTCTGAACCTCAGGCCCACCTTTTCTCATGTCTGGCAGCTGCTCTGCTCTAGACCCTGCTCATCTCCACATCCTAAATGTTCACTTTCTATGTCTTTCCCTTTCTAGCTCTA) c.*28+1902_*28+2038delinsTGCTTTGCTGTGTGGGGGTCCATGGCTCTGAACCTCAGGCCCACCTTTTCTCATGTCTGGCAGCTGCTCTGCTCTAGACCCTGCTCATCTCCACATCCTAAATGTTCACTTTCTATGTCTTTCCCTTTCTAGCTCTA (n.*28+1902_*28+2038delinsTGCTTTGCTGTGTGGGGGTCCATGGCTCTGAACCTCAGGCCCACCTTTTCTCATGTCTGGCAGCTGCTCTGCTCTAGACCCTGCTCATCTCCACATCCTAAATGTTCACTTTCTATGTCTTTCCCTTTCTAGCTCTA) c.2148+10_2148+146delinsTGCTTTGCTGTGTGGGGGTCCATGGCTCTGAACCTCAGGCCCACCTTTTCTCATGTCTGGCAGCTGCTCTGCTCTAGACCCTGCTCATCTCCACATCCTAAATGTTCACTTTCTATGTCTTTCCCTTTCTAGCTCTA (n.2148+10_2148+146delinsTGCTTTGCTGTGTGGGGGTCCATGGCTCTGAACCTCAGGCCCACCTTTTCTCATGTCTGGCAGCTGCTCTGCTCTAGACCCTGCTCATCTCCACATCCTAAATGTTCACTTTCTATGTCTTTCCCTTTCTAGCTCTA) c.1482+10_1482+146delinsTGCTTTGCTGTGTGGGGGTCCATGGCTCTGAACCTCAGGCCCACCTTTTCTCATGTCTGGCAGCTGCTCTGCTCTAGACCCTGCTCATCTCCACATCCTAAATGTTCACTTTCTATGTCTTTCCCTTTCTAGCTCTA (n.1482+10_1482+146delinsTGCTTTGCTGTGTGGGGGTCCATGGCTCTGAACCTCAGGCCCACCTTTTCTCATGTCTGGCAGCTGCTCTGCTCTAGACCCTGCTCATCTCCACATCCTAAATGTTCACTTTCTATGTCTTTCCCTTTCTAGCTCTA) | |
7 | g.55174831G>A | CA158932710 | EGFR | c.2124+11G>A (n.2124+11G>A) c.632+11G>A c.2283+11G>A (n.2283+11G>A) c.*28+1903G>A (n.*28+1903G>A) c.2148+11G>A (n.2148+11G>A) c.1482+11G>A (n.1482+11G>A) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
7 | g.55174831G>C | CA2580077263 | EGFR | c.2124+11G>C (n.2124+11G>C) c.632+11G>C c.2283+11G>C (n.2283+11G>C) c.*28+1903G>C (n.*28+1903G>C) c.2148+11G>C (n.2148+11G>C) c.1482+11G>C (n.1482+11G>C) | ClinVar dbSNP gnomAD v4 |
7 | g.55174831G= | CA1708918382 | EGFR | c.2124+11G= (n.2124+11G=) c.632+11G= c.2283+11G= (n.2283+11G=) c.*28+1903G= (n.*28+1903G=) c.2148+11G= (n.2148+11G=) c.1482+11G= (n.1482+11G=) | |
7 | g.55174831G>T | CA2714507806 | EGFR | c.2124+11G>T (n.2124+11G>T) c.632+11G>T c.2283+11G>T (n.2283+11G>T) c.*28+1903G>T (n.*28+1903G>T) c.2148+11G>T (n.2148+11G>T) c.1482+11G>T (n.1482+11G>T) | dbSNP |
7 | g.55174832_55174967del | CA135830 | EGFR | c.2124+12_2124+147del (n.2124+12_2124+147del) c.632+12_632+147del c.2283+12_2283+147del (n.2283+12_2283+147del) c.*28+1904_*28+2039del (n.*28+1904_*28+2039del) c.2148+12_2148+147del (n.2148+12_2148+147del) c.1482+12_1482+147del (n.1482+12_1482+147del) | ClinVar dbSNP |
7 | g.55174832C>A | CA2578893555 | EGFR | c.2124+12C>A (n.2124+12C>A) c.632+12C>A c.2283+12C>A (n.2283+12C>A) c.*28+1904C>A (n.*28+1904C>A) c.2148+12C>A (n.2148+12C>A) c.1482+12C>A (n.1482+12C>A) | dbSNP |
7 | g.55174832C= | CA1708918383 | EGFR | c.2124+12C= (n.2124+12C=) c.632+12C= c.2283+12C= (n.2283+12C=) c.*28+1904C= (n.*28+1904C=) c.2148+12C= (n.2148+12C=) c.1482+12C= (n.1482+12C=) | |
7 | g.55174832C>G | CA2714512066 | EGFR | c.2124+12C>G (n.2124+12C>G) c.632+12C>G c.2283+12C>G (n.2283+12C>G) c.*28+1904C>G (n.*28+1904C>G) c.2148+12C>G (n.2148+12C>G) c.1482+12C>G (n.1482+12C>G) | dbSNP |
7 | g.55174832C>T | CA158932713 | EGFR | c.2124+12C>T (n.2124+12C>T) c.632+12C>T c.2283+12C>T (n.2283+12C>T) c.*28+1904C>T (n.*28+1904C>T) c.2148+12C>T (n.2148+12C>T) c.1482+12C>T (n.1482+12C>T) | ClinVar dbSNP gnomAD v4 |
7 | g.55174832_55174833delinsCT | CA1708918384 | EGFR | c.2124+12_2124+13delinsCT (n.2124+12_2124+13delinsCT) c.632+12_632+13delinsCT c.2283+12_2283+13delinsCT (n.2283+12_2283+13delinsCT) c.*28+1904_*28+1905delinsCT (n.*28+1904_*28+1905delinsCT) c.2148+12_2148+13delinsCT (n.2148+12_2148+13delinsCT) c.1482+12_1482+13delinsCT (n.1482+12_1482+13delinsCT) | |
7 | g.55174833T>A | CA2714960578 | EGFR | c.2124+13T>A (n.2124+13T>A) c.632+13T>A c.2283+13T>A (n.2283+13T>A) c.*28+1905T>A (n.*28+1905T>A) c.2148+13T>A (n.2148+13T>A) c.1482+13T>A (n.1482+13T>A) | dbSNP |
7 | g.55174835del | CA1101518244 | EGFR | c.2124+15del (n.2124+15del) c.632+15del c.2283+15del (n.2283+15del) c.*28+1907del (n.*28+1907del) c.2148+15del (n.2148+15del) c.1482+15del (n.1482+15del) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
7 | g.55174833_55174855delinsTTTGCTGTGTGGGGGTCCATGGC | CA1708918385 | EGFR | c.2124+13_2124+35delinsTTTGCTGTGTGGGGGTCCATGGC (n.2124+13_2124+35delinsTTTGCTGTGTGGGGGTCCATGGC) c.632+13_632+35delinsTTTGCTGTGTGGGGGTCCATGGC c.2283+13_2283+35delinsTTTGCTGTGTGGGGGTCCATGGC (n.2283+13_2283+35delinsTTTGCTGTGTGGGGGTCCATGGC) c.*28+1905_*28+1927delinsTTTGCTGTGTGGGGGTCCATGGC (n.*28+1905_*28+1927delinsTTTGCTGTGTGGGGGTCCATGGC) c.2148+13_2148+35delinsTTTGCTGTGTGGGGGTCCATGGC (n.2148+13_2148+35delinsTTTGCTGTGTGGGGGTCCATGGC) c.1482+13_1482+35delinsTTTGCTGTGTGGGGGTCCATGGC (n.1482+13_1482+35delinsTTTGCTGTGTGGGGGTCCATGGC) | |
7 | g.55174834T>A | CA2714960594 | EGFR | c.2124+14T>A (n.2124+14T>A) c.632+14T>A c.2283+14T>A (n.2283+14T>A) c.*28+1906T>A (n.*28+1906T>A) c.2148+14T>A (n.2148+14T>A) c.1482+14T>A (n.1482+14T>A) | dbSNP |
7 | g.55174834T>C | CA2714960596 | EGFR | c.2124+14T>C (n.2124+14T>C) c.632+14T>C c.2283+14T>C (n.2283+14T>C) c.*28+1906T>C (n.*28+1906T>C) c.2148+14T>C (n.2148+14T>C) c.1482+14T>C (n.1482+14T>C) | dbSNP |
7 | g.55174835_55174856del | CA4266025 | EGFR | c.2124+15_2124+36del (n.2124+15_2124+36del) c.632+15_632+36del c.2283+15_2283+36del (n.2283+15_2283+36del) c.*28+1907_*28+1928del (n.*28+1907_*28+1928del) c.2148+15_2148+36del (n.2148+15_2148+36del) c.1482+15_1482+36del (n.1482+15_1482+36del) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
7 | g.55174835T>A | CA2714960597 | EGFR | c.2124+15T>A (n.2124+15T>A) c.632+15T>A c.2283+15T>A (n.2283+15T>A) c.*28+1907T>A (n.*28+1907T>A) c.2148+15T>A (n.2148+15T>A) c.1482+15T>A (n.1482+15T>A) | dbSNP |
7 | g.55174835T>C | CA2682854899 | EGFR | c.2124+15T>C (n.2124+15T>C) c.632+15T>C c.2283+15T>C (n.2283+15T>C) c.*28+1907T>C (n.*28+1907T>C) c.2148+15T>C (n.2148+15T>C) c.1482+15T>C (n.1482+15T>C) | gnomAD v4 |
7 | g.55174836G>A | CA2578893556 | EGFR | c.2124+16G>A (n.2124+16G>A) c.632+16G>A c.2283+16G>A (n.2283+16G>A) c.*28+1908G>A (n.*28+1908G>A) c.2148+16G>A (n.2148+16G>A) c.1482+16G>A (n.1482+16G>A) | dbSNP |
7 | g.55174836G>C | CA2714960603 | EGFR | c.2124+16G>C (n.2124+16G>C) c.632+16G>C c.2283+16G>C (n.2283+16G>C) c.*28+1908G>C (n.*28+1908G>C) c.2148+16G>C (n.2148+16G>C) c.1482+16G>C (n.1482+16G>C) | dbSNP |
7 | g.55174836G>T | CA2714960604 | EGFR | c.2124+16G>T (n.2124+16G>T) c.632+16G>T c.2283+16G>T (n.2283+16G>T) c.*28+1908G>T (n.*28+1908G>T) c.2148+16G>T (n.2148+16G>T) c.1482+16G>T (n.1482+16G>T) | dbSNP |
7 | g.55174837C>A | CA2682854900 | EGFR | c.2124+17C>A (n.2124+17C>A) c.632+17C>A c.2283+17C>A (n.2283+17C>A) c.*28+1909C>A (n.*28+1909C>A) c.2148+17C>A (n.2148+17C>A) c.1482+17C>A (n.1482+17C>A) | dbSNP gnomAD v4 |
7 | g.55174837C= | CA1708918387 | EGFR | c.2124+17C= (n.2124+17C=) c.632+17C= c.2283+17C= (n.2283+17C=) c.*28+1909C= (n.*28+1909C=) c.2148+17C= (n.2148+17C=) c.1482+17C= (n.1482+17C=) | |
7 | g.55174837C>G | CA2714563570 | EGFR | c.2124+17C>G (n.2124+17C>G) c.632+17C>G c.2283+17C>G (n.2283+17C>G) c.*28+1909C>G (n.*28+1909C>G) c.2148+17C>G (n.2148+17C>G) c.1482+17C>G (n.1482+17C>G) | dbSNP |
7 | g.55174837C>T | CA574335588 | EGFR | c.2124+17C>T (n.2124+17C>T) c.632+17C>T c.2283+17C>T (n.2283+17C>T) c.*28+1909C>T (n.*28+1909C>T) c.2148+17C>T (n.2148+17C>T) c.1482+17C>T (n.1482+17C>T) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
7 | g.55174837_55174840delinsCTGT | CA1708918386 | EGFR | c.2124+17_2124+20delinsCTGT (n.2124+17_2124+20delinsCTGT) c.632+17_632+20delinsCTGT c.2283+17_2283+20delinsCTGT (n.2283+17_2283+20delinsCTGT) c.*28+1909_*28+1912delinsCTGT (n.*28+1909_*28+1912delinsCTGT) c.2148+17_2148+20delinsCTGT (n.2148+17_2148+20delinsCTGT) c.1482+17_1482+20delinsCTGT (n.1482+17_1482+20delinsCTGT) | |
7 | g.55174838T>A | CA2714512070 | EGFR | c.2124+18T>A (n.2124+18T>A) c.632+18T>A c.2283+18T>A (n.2283+18T>A) c.*28+1910T>A (n.*28+1910T>A) c.2148+18T>A (n.2148+18T>A) c.1482+18T>A (n.1482+18T>A) | dbSNP |
7 | g.55174838T>C | CA4266027 | EGFR | c.2124+18T>C (n.2124+18T>C) c.632+18T>C c.2283+18T>C (n.2283+18T>C) c.*28+1910T>C (n.*28+1910T>C) c.2148+18T>C (n.2148+18T>C) c.1482+18T>C (n.1482+18T>C) | dbSNP ExAC gnomAD v2 gnomAD v4 |
7 | g.55174838T>G | CA2714512068 | EGFR | c.2124+18T>G (n.2124+18T>G) c.632+18T>G c.2283+18T>G (n.2283+18T>G) c.*28+1910T>G (n.*28+1910T>G) c.2148+18T>G (n.2148+18T>G) c.1482+18T>G (n.1482+18T>G) | dbSNP |
7 | g.55174838T= | CA1708918388 | EGFR | c.2124+18T= (n.2124+18T=) c.632+18T= c.2283+18T= (n.2283+18T=) c.*28+1910T= (n.*28+1910T=) c.2148+18T= (n.2148+18T=) c.1482+18T= (n.1482+18T=) | |
7 | g.55174838_55174840del | CA4266026 | EGFR | c.2124+18_2124+20del (n.2124+18_2124+20del) c.632+18_632+20del c.2283+18_2283+20del (n.2283+18_2283+20del) c.*28+1910_*28+1912del (n.*28+1910_*28+1912del) c.2148+18_2148+20del (n.2148+18_2148+20del) c.1482+18_1482+20del (n.1482+18_1482+20del) | dbSNP ExAC gnomAD v2 gnomAD v4 |
7 | g.55174839G>A | CA1101518257 | EGFR | c.2124+19G>A (n.2124+19G>A) c.632+19G>A c.2283+19G>A (n.2283+19G>A) c.*28+1911G>A (n.*28+1911G>A) c.2148+19G>A (n.2148+19G>A) c.1482+19G>A (n.1482+19G>A) | dbSNP gnomAD v3 gnomAD v4 |
7 | g.55174839G>C | CA2682854902 | EGFR | c.2124+19G>C (n.2124+19G>C) c.632+19G>C c.2283+19G>C (n.2283+19G>C) c.*28+1911G>C (n.*28+1911G>C) c.2148+19G>C (n.2148+19G>C) c.1482+19G>C (n.1482+19G>C) | dbSNP gnomAD v4 |
7 | g.55174839G= | CA1708918389 | EGFR | c.2124+19G= (n.2124+19G=) c.632+19G= c.2283+19G= (n.2283+19G=) c.*28+1911G= (n.*28+1911G=) c.2148+19G= (n.2148+19G=) c.1482+19G= (n.1482+19G=) | |
7 | g.55174839G>T | CA2682854903 | EGFR | c.2124+19G>T (n.2124+19G>T) c.632+19G>T c.2283+19G>T (n.2283+19G>T) c.*28+1911G>T (n.*28+1911G>T) c.2148+19G>T (n.2148+19G>T) c.1482+19G>T (n.1482+19G>T) | gnomAD v4 |
7 | g.55174840T>A | CA2714530344 | EGFR | c.2124+20T>A (n.2124+20T>A) c.632+20T>A c.2283+20T>A (n.2283+20T>A) c.*28+1912T>A (n.*28+1912T>A) c.2148+20T>A (n.2148+20T>A) c.1482+20T>A (n.1482+20T>A) | dbSNP |
7 | g.55174840T>C | CA574335589 | EGFR | c.2124+20T>C (n.2124+20T>C) c.632+20T>C c.2283+20T>C (n.2283+20T>C) c.*28+1912T>C (n.*28+1912T>C) c.2148+20T>C (n.2148+20T>C) c.1482+20T>C (n.1482+20T>C) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
7 | g.55174840T>G | CA2714530345 | EGFR | c.2124+20T>G (n.2124+20T>G) c.632+20T>G c.2283+20T>G (n.2283+20T>G) c.*28+1912T>G (n.*28+1912T>G) c.2148+20T>G (n.2148+20T>G) c.1482+20T>G (n.1482+20T>G) | dbSNP |
7 | g.55174840T= | CA1708918390 | EGFR | c.2124+20T= (n.2124+20T=) c.632+20T= c.2283+20T= (n.2283+20T=) c.*28+1912T= (n.*28+1912T=) c.2148+20T= (n.2148+20T=) c.1482+20T= (n.1482+20T=) | |
7 | g.55174841G>A | CA2714960607 | EGFR | c.2124+21G>A (n.2124+21G>A) c.632+21G>A c.2283+21G>A (n.2283+21G>A) c.*28+1913G>A (n.*28+1913G>A) c.2148+21G>A (n.2148+21G>A) c.1482+21G>A (n.1482+21G>A) | dbSNP |
7 | g.55174841G>C | CA2714960608 | EGFR | c.2124+21G>C (n.2124+21G>C) c.632+21G>C c.2283+21G>C (n.2283+21G>C) c.*28+1913G>C (n.*28+1913G>C) c.2148+21G>C (n.2148+21G>C) c.1482+21G>C (n.1482+21G>C) | dbSNP |
7 | g.55174841G>T | CA2578893557 | EGFR | c.2124+21G>T (n.2124+21G>T) c.632+21G>T c.2283+21G>T (n.2283+21G>T) c.*28+1913G>T (n.*28+1913G>T) c.2148+21G>T (n.2148+21G>T) c.1482+21G>T (n.1482+21G>T) | gnomAD v4 |
7 | g.55174842dup | CA2775498839 | EGFR | c.2124+22dup (n.2124+22dup) c.632+22dup c.2283+22dup (n.2283+22dup) c.*28+1914dup (n.*28+1914dup) c.2148+22dup (n.2148+22dup) c.1482+22dup (n.1482+22dup) | |
7 | g.55174842_55174843delinsTG | CA1708918391 | EGFR | c.2124+22_2124+23delinsTG (n.2124+22_2124+23delinsTG) c.632+22_632+23delinsTG c.2283+22_2283+23delinsTG (n.2283+22_2283+23delinsTG) c.*28+1914_*28+1915delinsTG (n.*28+1914_*28+1915delinsTG) c.2148+22_2148+23delinsTG (n.2148+22_2148+23delinsTG) c.1482+22_1482+23delinsTG (n.1482+22_1482+23delinsTG) | |
7 | g.55174843G>A | CA2682854904 | EGFR | c.2124+23G>A (n.2124+23G>A) c.632+23G>A c.2283+23G>A (n.2283+23G>A) c.*28+1915G>A (n.*28+1915G>A) c.2148+23G>A (n.2148+23G>A) c.1482+23G>A (n.1482+23G>A) | dbSNP gnomAD v4 |
7 | g.55174843G>C | CA4266028 | EGFR | c.2124+23G>C (n.2124+23G>C) c.632+23G>C c.2283+23G>C (n.2283+23G>C) c.*28+1915G>C (n.*28+1915G>C) c.2148+23G>C (n.2148+23G>C) c.1482+23G>C (n.1482+23G>C) | dbSNP ExAC gnomAD v2 gnomAD v4 |
7 | g.55174843G= | CA1708918392 | EGFR | c.2124+23G= (n.2124+23G=) c.632+23G= c.2283+23G= (n.2283+23G=) c.*28+1915G= (n.*28+1915G=) c.2148+23G= (n.2148+23G=) c.1482+23G= (n.1482+23G=) | |
7 | g.55174843G>T | CA1708918393 | EGFR | c.2124+23G>T (n.2124+23G>T) c.632+23G>T c.2283+23G>T (n.2283+23G>T) c.*28+1915G>T (n.*28+1915G>T) c.2148+23G>T (n.2148+23G>T) c.1482+23G>T (n.1482+23G>T) | dbSNP |
7 | g.55174847dup | CA2775498840 | EGFR | c.2124+27dup (n.2124+27dup) c.632+27dup c.2283+27dup (n.2283+27dup) c.*28+1919dup (n.*28+1919dup) c.2148+27dup (n.2148+27dup) c.1482+27dup (n.1482+27dup) | |
7 | g.55174847del | CA574335590 | EGFR | c.2124+27del (n.2124+27del) c.632+27del c.2283+27del (n.2283+27del) c.*28+1919del (n.*28+1919del) c.2148+27del (n.2148+27del) c.1482+27del (n.1482+27del) | dbSNP gnomAD v2 gnomAD v4 |
7 | g.55174844G>A | CA645561555 | EGFR | c.2124+24G>A (n.2124+24G>A) c.632+24G>A c.2283+24G>A (n.2283+24G>A) c.*28+1916G>A (n.*28+1916G>A) c.2148+24G>A (n.2148+24G>A) c.1482+24G>A (n.1482+24G>A) | dbSNP gnomAD v4 COSMIC |
7 | g.55174844G>C | CA2682854906 | EGFR | c.2124+24G>C (n.2124+24G>C) c.632+24G>C c.2283+24G>C (n.2283+24G>C) c.*28+1916G>C (n.*28+1916G>C) c.2148+24G>C (n.2148+24G>C) c.1482+24G>C (n.1482+24G>C) | dbSNP gnomAD v4 |
7 | g.55174844G>T | CA2682854905 | EGFR | c.2124+24G>T (n.2124+24G>T) c.632+24G>T c.2283+24G>T (n.2283+24G>T) c.*28+1916G>T (n.*28+1916G>T) c.2148+24G>T (n.2148+24G>T) c.1482+24G>T (n.1482+24G>T) | dbSNP gnomAD v4 |
7 | g.55174845G>A | CA1708918395 | EGFR | c.2124+25G>A (n.2124+25G>A) c.632+25G>A c.2283+25G>A (n.2283+25G>A) c.*28+1917G>A (n.*28+1917G>A) c.2148+25G>A (n.2148+25G>A) c.1482+25G>A (n.1482+25G>A) | dbSNP |
7 | g.55174845G>C | CA2714593845 | EGFR | c.2124+25G>C (n.2124+25G>C) c.632+25G>C c.2283+25G>C (n.2283+25G>C) c.*28+1917G>C (n.*28+1917G>C) c.2148+25G>C (n.2148+25G>C) c.1482+25G>C (n.1482+25G>C) | dbSNP |
7 | g.55174845G= | CA1708918394 | EGFR | c.2124+25G= (n.2124+25G=) c.632+25G= c.2283+25G= (n.2283+25G=) c.*28+1917G= (n.*28+1917G=) c.2148+25G= (n.2148+25G=) c.1482+25G= (n.1482+25G=) | |
7 | g.55174845G>T | CA2714593847 | EGFR | c.2124+25G>T (n.2124+25G>T) c.632+25G>T c.2283+25G>T (n.2283+25G>T) c.*28+1917G>T (n.*28+1917G>T) c.2148+25G>T (n.2148+25G>T) c.1482+25G>T (n.1482+25G>T) | dbSNP |
7 | g.55174845_55174846insTGTGTTT | CA2775498841 | EGFR | c.2124+25_2124+26insTGTGTTT (n.2124+25_2124+26insTGTGTTT) c.632+25_632+26insTGTGTTT c.2283+25_2283+26insTGTGTTT (n.2283+25_2283+26insTGTGTTT) c.*28+1917_*28+1918insTGTGTTT (n.*28+1917_*28+1918insTGTGTTT) c.2148+25_2148+26insTGTGTTT (n.2148+25_2148+26insTGTGTTT) c.1482+25_1482+26insTGTGTTT (n.1482+25_1482+26insTGTGTTT) | |
7 | g.55174846G>A | CA2682854907 | EGFR | c.2124+26G>A (n.2124+26G>A) c.632+26G>A c.2283+26G>A (n.2283+26G>A) c.*28+1918G>A (n.*28+1918G>A) c.2148+26G>A (n.2148+26G>A) c.1482+26G>A (n.1482+26G>A) | dbSNP gnomAD v4 |
7 | g.55174846G>C | CA2714960613 | EGFR | c.2124+26G>C (n.2124+26G>C) c.632+26G>C c.2283+26G>C (n.2283+26G>C) c.*28+1918G>C (n.*28+1918G>C) c.2148+26G>C (n.2148+26G>C) c.1482+26G>C (n.1482+26G>C) | dbSNP |
7 | g.55174846G>T | CA2714960616 | EGFR | c.2124+26G>T (n.2124+26G>T) c.632+26G>T c.2283+26G>T (n.2283+26G>T) c.*28+1918G>T (n.*28+1918G>T) c.2148+26G>T (n.2148+26G>T) c.1482+26G>T (n.1482+26G>T) | dbSNP |
7 | g.55174847G>A | CA2578893558 | EGFR | c.2124+27G>A (n.2124+27G>A) c.632+27G>A c.2283+27G>A (n.2283+27G>A) c.*28+1919G>A (n.*28+1919G>A) c.2148+27G>A (n.2148+27G>A) c.1482+27G>A (n.1482+27G>A) | dbSNP gnomAD v4 |
7 | g.55174847G>C | CA2714513301 | EGFR | c.2124+27G>C (n.2124+27G>C) c.632+27G>C c.2283+27G>C (n.2283+27G>C) c.*28+1919G>C (n.*28+1919G>C) c.2148+27G>C (n.2148+27G>C) c.1482+27G>C (n.1482+27G>C) | dbSNP |
7 | g.55174847G= | CA1708918396 | EGFR | c.2124+27G= (n.2124+27G=) c.632+27G= c.2283+27G= (n.2283+27G=) c.*28+1919G= (n.*28+1919G=) c.2148+27G= (n.2148+27G=) c.1482+27G= (n.1482+27G=) | |
7 | g.55174847G>T | CA4266029 | EGFR | c.2124+27G>T (n.2124+27G>T) c.632+27G>T c.2283+27G>T (n.2283+27G>T) c.*28+1919G>T (n.*28+1919G>T) c.2148+27G>T (n.2148+27G>T) c.1482+27G>T (n.1482+27G>T) | dbSNP ExAC gnomAD v2 |
7 | g.55174848T>C | CA651109898 | EGFR | c.2124+28T>C (n.2124+28T>C) c.632+28T>C c.2283+28T>C (n.2283+28T>C) c.*28+1920T>C (n.*28+1920T>C) c.2148+28T>C (n.2148+28T>C) c.1482+28T>C (n.1482+28T>C) | dbSNP COSMIC |
7 | g.55174848T>G | CA2714960621 | EGFR | c.2124+28T>G (n.2124+28T>G) c.632+28T>G c.2283+28T>G (n.2283+28T>G) c.*28+1920T>G (n.*28+1920T>G) c.2148+28T>G (n.2148+28T>G) c.1482+28T>G (n.1482+28T>G) | dbSNP |
7 | g.55174849C>A | CA2714960622 | EGFR | c.2124+29C>A (n.2124+29C>A) c.632+29C>A c.2283+29C>A (n.2283+29C>A) c.*28+1921C>A (n.*28+1921C>A) c.2148+29C>A (n.2148+29C>A) c.1482+29C>A (n.1482+29C>A) | dbSNP |
7 | g.55174849C>G | CA2714960624 | EGFR | c.2124+29C>G (n.2124+29C>G) c.632+29C>G c.2283+29C>G (n.2283+29C>G) c.*28+1921C>G (n.*28+1921C>G) c.2148+29C>G (n.2148+29C>G) c.1482+29C>G (n.1482+29C>G) | dbSNP |
7 | g.55174849C>T | CA2714960623 | EGFR | c.2124+29C>T (n.2124+29C>T) c.632+29C>T c.2283+29C>T (n.2283+29C>T) c.*28+1921C>T (n.*28+1921C>T) c.2148+29C>T (n.2148+29C>T) c.1482+29C>T (n.1482+29C>T) | dbSNP |
7 | g.55174850C>A | CA2682854908 | EGFR | c.2124+30C>A (n.2124+30C>A) c.632+30C>A c.2283+30C>A (n.2283+30C>A) c.*28+1922C>A (n.*28+1922C>A) c.2148+30C>A (n.2148+30C>A) c.1482+30C>A (n.1482+30C>A) | dbSNP gnomAD v4 |
7 | g.55174850C>G | CA2714960625 | EGFR | c.2124+30C>G (n.2124+30C>G) c.632+30C>G c.2283+30C>G (n.2283+30C>G) c.*28+1922C>G (n.*28+1922C>G) c.2148+30C>G (n.2148+30C>G) c.1482+30C>G (n.1482+30C>G) | dbSNP |
7 | g.55174850C>T | CA2714960626 | EGFR | c.2124+30C>T (n.2124+30C>T) c.632+30C>T c.2283+30C>T (n.2283+30C>T) c.*28+1922C>T (n.*28+1922C>T) c.2148+30C>T (n.2148+30C>T) c.1482+30C>T (n.1482+30C>T) | dbSNP |
7 | g.55174851A= | CA1708918397 | EGFR | c.2124+31A= (n.2124+31A=) c.632+31A= c.2283+31A= (n.2283+31A=) c.*28+1923A= (n.*28+1923A=) c.2148+31A= (n.2148+31A=) c.1482+31A= (n.1482+31A=) | |
7 | g.55174851A>C | CA574335594 | EGFR | c.2124+31A>C (n.2124+31A>C) c.632+31A>C c.2283+31A>C (n.2283+31A>C) c.*28+1923A>C (n.*28+1923A>C) c.2148+31A>C (n.2148+31A>C) c.1482+31A>C (n.1482+31A>C) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
7 | g.55174851A>G | CA4266030 | EGFR | c.2124+31A>G (n.2124+31A>G) c.632+31A>G c.2283+31A>G (n.2283+31A>G) c.*28+1923A>G (n.*28+1923A>G) c.2148+31A>G (n.2148+31A>G) c.1482+31A>G (n.1482+31A>G) | dbSNP ExAC gnomAD v2 gnomAD v4 |
7 | g.55174851A>T | CA2714512077 | EGFR | c.2124+31A>T (n.2124+31A>T) c.632+31A>T c.2283+31A>T (n.2283+31A>T) c.*28+1923A>T (n.*28+1923A>T) c.2148+31A>T (n.2148+31A>T) c.1482+31A>T (n.1482+31A>T) | dbSNP |
7 | g.55174852T>C | CA2561491833 | EGFR | c.2124+32T>C (n.2124+32T>C) c.632+32T>C c.2283+32T>C (n.2283+32T>C) c.*28+1924T>C (n.*28+1924T>C) c.2148+32T>C (n.2148+32T>C) c.1482+32T>C (n.1482+32T>C) | gnomAD v4 |
7 | g.55174853G>A | CA2682854909 | EGFR | c.2124+33G>A (n.2124+33G>A) c.632+33G>A c.2283+33G>A (n.2283+33G>A) c.*28+1925G>A (n.*28+1925G>A) c.2148+33G>A (n.2148+33G>A) c.1482+33G>A (n.1482+33G>A) | dbSNP gnomAD v4 |
7 | g.55174853G>C | CA2714960627 | EGFR | c.2124+33G>C (n.2124+33G>C) c.632+33G>C c.2283+33G>C (n.2283+33G>C) c.*28+1925G>C (n.*28+1925G>C) c.2148+33G>C (n.2148+33G>C) c.1482+33G>C (n.1482+33G>C) | dbSNP |
7 | g.55174853G>T | CA2682854910 | EGFR | c.2124+33G>T (n.2124+33G>T) c.632+33G>T c.2283+33G>T (n.2283+33G>T) c.*28+1925G>T (n.*28+1925G>T) c.2148+33G>T (n.2148+33G>T) c.1482+33G>T (n.1482+33G>T) | gnomAD v4 |
7 | g.55174854del | CA2578893559 | EGFR | c.2124+34del (n.2124+34del) c.632+34del c.2283+34del (n.2283+34del) c.*28+1926del (n.*28+1926del) c.2148+34del (n.2148+34del) c.1482+34del (n.1482+34del) | |
7 | g.55174854G>A | CA2714960628 | EGFR | c.2124+34G>A (n.2124+34G>A) c.632+34G>A c.2283+34G>A (n.2283+34G>A) c.*28+1926G>A (n.*28+1926G>A) c.2148+34G>A (n.2148+34G>A) c.1482+34G>A (n.1482+34G>A) | dbSNP |
7 | g.55174854G>C | CA2714960679 | EGFR | c.2124+34G>C (n.2124+34G>C) c.632+34G>C c.2283+34G>C (n.2283+34G>C) c.*28+1926G>C (n.*28+1926G>C) c.2148+34G>C (n.2148+34G>C) c.1482+34G>C (n.1482+34G>C) | dbSNP |
7 | g.55174854G>T | CA2578893560 | EGFR | c.2124+34G>T (n.2124+34G>T) c.632+34G>T c.2283+34G>T (n.2283+34G>T) c.*28+1926G>T (n.*28+1926G>T) c.2148+34G>T (n.2148+34G>T) c.1482+34G>T (n.1482+34G>T) | dbSNP |
7 | g.55174855C>A | CA2682854911 | EGFR | c.2124+35C>A (n.2124+35C>A) c.632+35C>A c.2283+35C>A (n.2283+35C>A) c.*28+1927C>A (n.*28+1927C>A) c.2148+35C>A (n.2148+35C>A) c.1482+35C>A (n.1482+35C>A) | dbSNP gnomAD v4 |
7 | g.55174855C>G | CA2714960680 | EGFR | c.2124+35C>G (n.2124+35C>G) c.632+35C>G c.2283+35C>G (n.2283+35C>G) c.*28+1927C>G (n.*28+1927C>G) c.2148+35C>G (n.2148+35C>G) c.1482+35C>G (n.1482+35C>G) | dbSNP |
7 | g.55174855C>T | CA2682854912 | EGFR | c.2124+35C>T (n.2124+35C>T) c.632+35C>T c.2283+35C>T (n.2283+35C>T) c.*28+1927C>T (n.*28+1927C>T) c.2148+35C>T (n.2148+35C>T) c.1482+35C>T (n.1482+35C>T) | dbSNP gnomAD v4 |
7 | g.55174856T>A | CA2578893561 | EGFR | c.2124+36T>A (n.2124+36T>A) c.632+36T>A c.2283+36T>A (n.2283+36T>A) c.*28+1928T>A (n.*28+1928T>A) c.2148+36T>A (n.2148+36T>A) c.1482+36T>A (n.1482+36T>A) | dbSNP |
7 | g.55174856T>C | CA4266031 | EGFR | c.2124+36T>C (n.2124+36T>C) c.632+36T>C c.2283+36T>C (n.2283+36T>C) c.*28+1928T>C (n.*28+1928T>C) c.2148+36T>C (n.2148+36T>C) c.1482+36T>C (n.1482+36T>C) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
7 | g.55174856T= | CA1708918398 | EGFR | c.2124+36T= (n.2124+36T=) c.632+36T= c.2283+36T= (n.2283+36T=) c.*28+1928T= (n.*28+1928T=) c.2148+36T= (n.2148+36T=) c.1482+36T= (n.1482+36T=) | |
7 | g.55174856_55174864del | CA2682854913 | EGFR | c.2124+36_2124+44del (n.2124+36_2124+44del) c.632+36_632+44del c.2283+36_2283+44del (n.2283+36_2283+44del) c.*28+1928_*28+1936del (n.*28+1928_*28+1936del) c.2148+36_2148+44del (n.2148+36_2148+44del) c.1482+36_1482+44del (n.1482+36_1482+44del) | gnomAD v4 |
7 | g.55174857C>G | CA2682854914 | EGFR | c.2124+37C>G (n.2124+37C>G) c.632+37C>G c.2283+37C>G (n.2283+37C>G) c.*28+1929C>G (n.*28+1929C>G) c.2148+37C>G (n.2148+37C>G) c.1482+37C>G (n.1482+37C>G) | dbSNP gnomAD v4 |
7 | g.55174857C>T | CA2682854915 | EGFR | c.2124+37C>T (n.2124+37C>T) c.632+37C>T c.2283+37C>T (n.2283+37C>T) c.*28+1929C>T (n.*28+1929C>T) c.2148+37C>T (n.2148+37C>T) c.1482+37C>T (n.1482+37C>T) | dbSNP gnomAD v4 |
7 | g.55174858T>A | CA2714960682 | EGFR | c.2124+38T>A (n.2124+38T>A) c.632+38T>A c.2283+38T>A (n.2283+38T>A) c.*28+1930T>A (n.*28+1930T>A) c.2148+38T>A (n.2148+38T>A) c.1482+38T>A (n.1482+38T>A) | dbSNP |
7 | g.55174858T>C | CA2714960681 | EGFR | c.2124+38T>C (n.2124+38T>C) c.632+38T>C c.2283+38T>C (n.2283+38T>C) c.*28+1930T>C (n.*28+1930T>C) c.2148+38T>C (n.2148+38T>C) c.1482+38T>C (n.1482+38T>C) | dbSNP |
7 | g.55174859G>A | CA4266032 | EGFR | c.2124+39G>A (n.2124+39G>A) c.632+39G>A c.2283+39G>A (n.2283+39G>A) c.*28+1931G>A (n.*28+1931G>A) c.2148+39G>A (n.2148+39G>A) c.1482+39G>A (n.1482+39G>A) | dbSNP ExAC gnomAD v2 |
7 | g.55174859G>C | CA2714513302 | EGFR | c.2124+39G>C (n.2124+39G>C) c.632+39G>C c.2283+39G>C (n.2283+39G>C) c.*28+1931G>C (n.*28+1931G>C) c.2148+39G>C (n.2148+39G>C) c.1482+39G>C (n.1482+39G>C) | dbSNP |
7 | g.55174859G= | CA1708918399 | EGFR | c.2124+39G= (n.2124+39G=) c.632+39G= c.2283+39G= (n.2283+39G=) c.*28+1931G= (n.*28+1931G=) c.2148+39G= (n.2148+39G=) c.1482+39G= (n.1482+39G=) | |
7 | g.55174860A>C | CA2714960687 | EGFR | c.2124+40A>C (n.2124+40A>C) c.632+40A>C c.2283+40A>C (n.2283+40A>C) c.*28+1932A>C (n.*28+1932A>C) c.2148+40A>C (n.2148+40A>C) c.1482+40A>C (n.1482+40A>C) | dbSNP |
7 | g.55174860A>G | CA2578893562 | EGFR | c.2124+40A>G (n.2124+40A>G) c.632+40A>G c.2283+40A>G (n.2283+40A>G) c.*28+1932A>G (n.*28+1932A>G) c.2148+40A>G (n.2148+40A>G) c.1482+40A>G (n.1482+40A>G) | dbSNP |
7 | g.55174860A>T | CA2714960691 | EGFR | c.2124+40A>T (n.2124+40A>T) c.632+40A>T c.2283+40A>T (n.2283+40A>T) c.*28+1932A>T (n.*28+1932A>T) c.2148+40A>T (n.2148+40A>T) c.1482+40A>T (n.1482+40A>T) | dbSNP |
7 | g.55174861A>C | CA2714960694 | EGFR | c.2124+41A>C (n.2124+41A>C) c.632+41A>C c.2283+41A>C (n.2283+41A>C) c.*28+1933A>C (n.*28+1933A>C) c.2148+41A>C (n.2148+41A>C) c.1482+41A>C (n.1482+41A>C) | dbSNP |
7 | g.55174861A>G | CA2714960696 | EGFR | c.2124+41A>G (n.2124+41A>G) c.632+41A>G c.2283+41A>G (n.2283+41A>G) c.*28+1933A>G (n.*28+1933A>G) c.2148+41A>G (n.2148+41A>G) c.1482+41A>G (n.1482+41A>G) | dbSNP |
7 | g.55174861A>T | CA2714960711 | EGFR | c.2124+41A>T (n.2124+41A>T) c.632+41A>T c.2283+41A>T (n.2283+41A>T) c.*28+1933A>T (n.*28+1933A>T) c.2148+41A>T (n.2148+41A>T) c.1482+41A>T (n.1482+41A>T) | dbSNP |
7 | g.55174862C>A | CA2578893563 | EGFR | c.2124+42C>A (n.2124+42C>A) c.632+42C>A c.2283+42C>A (n.2283+42C>A) c.*28+1934C>A (n.*28+1934C>A) c.2148+42C>A (n.2148+42C>A) c.1482+42C>A (n.1482+42C>A) | gnomAD v4 |
7 | g.55174862C>T | CA2714960714 | EGFR | c.2124+42C>T (n.2124+42C>T) c.632+42C>T c.2283+42C>T (n.2283+42C>T) c.*28+1934C>T (n.*28+1934C>T) c.2148+42C>T (n.2148+42C>T) c.1482+42C>T (n.1482+42C>T) | dbSNP |
7 | g.55174863C>A | CA2578893564 | EGFR | c.2124+43C>A (n.2124+43C>A) c.632+43C>A c.2283+43C>A (n.2283+43C>A) c.*28+1935C>A (n.*28+1935C>A) c.2148+43C>A (n.2148+43C>A) c.1482+43C>A (n.1482+43C>A) | dbSNP gnomAD v4 |
7 | g.55174863C>G | CA2714960728 | EGFR | c.2124+43C>G (n.2124+43C>G) c.632+43C>G c.2283+43C>G (n.2283+43C>G) c.*28+1935C>G (n.*28+1935C>G) c.2148+43C>G (n.2148+43C>G) c.1482+43C>G (n.1482+43C>G) | dbSNP |
7 | g.55174863C>T | CA2682854916 | EGFR | c.2124+43C>T (n.2124+43C>T) c.632+43C>T c.2283+43C>T (n.2283+43C>T) c.*28+1935C>T (n.*28+1935C>T) c.2148+43C>T (n.2148+43C>T) c.1482+43C>T (n.1482+43C>T) | dbSNP gnomAD v4 |
7 | g.55174864T>A | CA2714960730 | EGFR | c.2124+44T>A (n.2124+44T>A) c.632+44T>A c.2283+44T>A (n.2283+44T>A) c.*28+1936T>A (n.*28+1936T>A) c.2148+44T>A (n.2148+44T>A) c.1482+44T>A (n.1482+44T>A) | dbSNP |
7 | g.55174864T>C | CA2714960737 | EGFR | c.2124+44T>C (n.2124+44T>C) c.632+44T>C c.2283+44T>C (n.2283+44T>C) c.*28+1936T>C (n.*28+1936T>C) c.2148+44T>C (n.2148+44T>C) c.1482+44T>C (n.1482+44T>C) | dbSNP |
7 | g.55174865C>A | CA2714960748 | EGFR | c.2124+45C>A (n.2124+45C>A) c.632+45C>A c.2283+45C>A (n.2283+45C>A) c.*28+1937C>A (n.*28+1937C>A) c.2148+45C>A (n.2148+45C>A) c.1482+45C>A (n.1482+45C>A) | dbSNP |
7 | g.55174865C>G | CA2578893565 | EGFR | c.2124+45C>G (n.2124+45C>G) c.632+45C>G c.2283+45C>G (n.2283+45C>G) c.*28+1937C>G (n.*28+1937C>G) c.2148+45C>G (n.2148+45C>G) c.1482+45C>G (n.1482+45C>G) | dbSNP |
7 | g.55174865C>T | CA2714960751 | EGFR | c.2124+45C>T (n.2124+45C>T) c.632+45C>T c.2283+45C>T (n.2283+45C>T) c.*28+1937C>T (n.*28+1937C>T) c.2148+45C>T (n.2148+45C>T) c.1482+45C>T (n.1482+45C>T) | dbSNP |
7 | g.55174866A>C | CA2714960766 | EGFR | c.2124+46A>C (n.2124+46A>C) c.632+46A>C c.2283+46A>C (n.2283+46A>C) c.*28+1938A>C (n.*28+1938A>C) c.2148+46A>C (n.2148+46A>C) c.1482+46A>C (n.1482+46A>C) | dbSNP |
7 | g.55174866A>G | CA2682854917 | EGFR | c.2124+46A>G (n.2124+46A>G) c.632+46A>G c.2283+46A>G (n.2283+46A>G) c.*28+1938A>G (n.*28+1938A>G) c.2148+46A>G (n.2148+46A>G) c.1482+46A>G (n.1482+46A>G) | dbSNP gnomAD v4 |
7 | g.55174866A>T | CA2714960763 | EGFR | c.2124+46A>T (n.2124+46A>T) c.632+46A>T c.2283+46A>T (n.2283+46A>T) c.*28+1938A>T (n.*28+1938A>T) c.2148+46A>T (n.2148+46A>T) c.1482+46A>T (n.1482+46A>T) | dbSNP |
7 | g.55174867G>A | CA2714960770 | EGFR | c.2124+47G>A (n.2124+47G>A) c.632+47G>A c.2283+47G>A (n.2283+47G>A) c.*28+1939G>A (n.*28+1939G>A) c.2148+47G>A (n.2148+47G>A) c.1482+47G>A (n.1482+47G>A) | dbSNP |
7 | g.55174867G>C | CA2714960772 | EGFR | c.2124+47G>C (n.2124+47G>C) c.632+47G>C c.2283+47G>C (n.2283+47G>C) c.*28+1939G>C (n.*28+1939G>C) c.2148+47G>C (n.2148+47G>C) c.1482+47G>C (n.1482+47G>C) | dbSNP |
7 | g.55174867G>T | CA2714960773 | EGFR | c.2124+47G>T (n.2124+47G>T) c.632+47G>T c.2283+47G>T (n.2283+47G>T) c.*28+1939G>T (n.*28+1939G>T) c.2148+47G>T (n.2148+47G>T) c.1482+47G>T (n.1482+47G>T) | dbSNP |
7 | g.55174868G>A | CA4266033 | EGFR | c.2124+48G>A (n.2124+48G>A) c.632+48G>A c.2283+48G>A (n.2283+48G>A) c.*28+1940G>A (n.*28+1940G>A) c.2148+48G>A (n.2148+48G>A) c.1482+48G>A (n.1482+48G>A) | dbSNP ExAC gnomAD v2 gnomAD v4 |
7 | g.55174868G= | CA1708918400 | EGFR | c.2124+48G= (n.2124+48G=) c.632+48G= c.2283+48G= (n.2283+48G=) c.*28+1940G= (n.*28+1940G=) c.2148+48G= (n.2148+48G=) c.1482+48G= (n.1482+48G=) | |
7 | g.55174868G>T | CA2714511604 | EGFR | c.2124+48G>T (n.2124+48G>T) c.632+48G>T c.2283+48G>T (n.2283+48G>T) c.*28+1940G>T (n.*28+1940G>T) c.2148+48G>T (n.2148+48G>T) c.1482+48G>T (n.1482+48G>T) | dbSNP |
7 | g.55174869C>A | CA2578893566 | EGFR | c.2124+49C>A (n.2124+49C>A) c.632+49C>A c.2283+49C>A (n.2283+49C>A) c.*28+1941C>A (n.*28+1941C>A) c.2148+49C>A (n.2148+49C>A) c.1482+49C>A (n.1482+49C>A) | dbSNP gnomAD v4 |
7 | g.55174869C>G | CA2714960779 | EGFR | c.2124+49C>G (n.2124+49C>G) c.632+49C>G c.2283+49C>G (n.2283+49C>G) c.*28+1941C>G (n.*28+1941C>G) c.2148+49C>G (n.2148+49C>G) c.1482+49C>G (n.1482+49C>G) | dbSNP |
7 | g.55174869C>T | CA2578893567 | EGFR | c.2124+49C>T (n.2124+49C>T) c.632+49C>T c.2283+49C>T (n.2283+49C>T) c.*28+1941C>T (n.*28+1941C>T) c.2148+49C>T (n.2148+49C>T) c.1482+49C>T (n.1482+49C>T) | dbSNP |
7 | g.55174870C>A | CA2682854918 | EGFR | c.2124+50C>A (n.2124+50C>A) c.632+50C>A c.2283+50C>A (n.2283+50C>A) c.*28+1942C>A (n.*28+1942C>A) c.2148+50C>A (n.2148+50C>A) c.1482+50C>A (n.1482+50C>A) | dbSNP gnomAD v4 |
7 | g.55174870C>G | CA2714960787 | EGFR | c.2124+50C>G (n.2124+50C>G) c.632+50C>G c.2283+50C>G (n.2283+50C>G) c.*28+1942C>G (n.*28+1942C>G) c.2148+50C>G (n.2148+50C>G) c.1482+50C>G (n.1482+50C>G) | dbSNP |
7 | g.55174870C>T | CA2714960788 | EGFR | c.2124+50C>T (n.2124+50C>T) c.632+50C>T c.2283+50C>T (n.2283+50C>T) c.*28+1942C>T (n.*28+1942C>T) c.2148+50C>T (n.2148+50C>T) c.1482+50C>T (n.1482+50C>T) | dbSNP |
7 | g.55174871C>A | CA2714960807 | EGFR | c.2124+51C>A (n.2124+51C>A) c.632+51C>A c.2283+51C>A (n.2283+51C>A) c.*28+1943C>A (n.*28+1943C>A) c.2148+51C>A (n.2148+51C>A) c.1482+51C>A (n.1482+51C>A) | dbSNP |
7 | g.55174871C>T | CA2714960790 | EGFR | c.2124+51C>T (n.2124+51C>T) c.632+51C>T c.2283+51C>T (n.2283+51C>T) c.*28+1943C>T (n.*28+1943C>T) c.2148+51C>T (n.2148+51C>T) c.1482+51C>T (n.1482+51C>T) | dbSNP |
7 | g.55174872A>C | CA2714960809 | EGFR | c.2124+52A>C (n.2124+52A>C) c.632+52A>C c.2283+52A>C (n.2283+52A>C) c.*28+1944A>C (n.*28+1944A>C) c.2148+52A>C (n.2148+52A>C) c.1482+52A>C (n.1482+52A>C) | dbSNP |
7 | g.55174872A>G | CA2714960810 | EGFR | c.2124+52A>G (n.2124+52A>G) c.632+52A>G c.2283+52A>G (n.2283+52A>G) c.*28+1944A>G (n.*28+1944A>G) c.2148+52A>G (n.2148+52A>G) c.1482+52A>G (n.1482+52A>G) | dbSNP |
7 | g.55174872A>T | CA2714960811 | EGFR | c.2124+52A>T (n.2124+52A>T) c.632+52A>T c.2283+52A>T (n.2283+52A>T) c.*28+1944A>T (n.*28+1944A>T) c.2148+52A>T (n.2148+52A>T) c.1482+52A>T (n.1482+52A>T) | dbSNP |
7 | g.55174873C>A | CA2682854919 | EGFR | c.2124+53C>A (n.2124+53C>A) c.632+53C>A c.2283+53C>A (n.2283+53C>A) c.*28+1945C>A (n.*28+1945C>A) c.2148+53C>A (n.2148+53C>A) c.1482+53C>A (n.1482+53C>A) | dbSNP gnomAD v4 |
7 | g.55174873C>G | CA2714960812 | EGFR | c.2124+53C>G (n.2124+53C>G) c.632+53C>G c.2283+53C>G (n.2283+53C>G) c.*28+1945C>G (n.*28+1945C>G) c.2148+53C>G (n.2148+53C>G) c.1482+53C>G (n.1482+53C>G) | dbSNP |
7 | g.55174873C>T | CA2682854920 | EGFR | c.2124+53C>T (n.2124+53C>T) c.632+53C>T c.2283+53C>T (n.2283+53C>T) c.*28+1945C>T (n.*28+1945C>T) c.2148+53C>T (n.2148+53C>T) c.1482+53C>T (n.1482+53C>T) | dbSNP gnomAD v4 |
7 | g.55174874C>A | CA2578893568 | EGFR | c.2124+54C>A (n.2124+54C>A) c.632+54C>A c.2283+54C>A (n.2283+54C>A) c.*28+1946C>A (n.*28+1946C>A) c.2148+54C>A (n.2148+54C>A) c.1482+54C>A (n.1482+54C>A) | dbSNP gnomAD v4 |
7 | g.55174874C= | CA1708918401 | EGFR | c.2124+54C= (n.2124+54C=) c.632+54C= c.2283+54C= (n.2283+54C=) c.*28+1946C= (n.*28+1946C=) c.2148+54C= (n.2148+54C=) c.1482+54C= (n.1482+54C=) | |
7 | g.55174874C>G | CA574335598 | EGFR | c.2124+54C>G (n.2124+54C>G) c.632+54C>G c.2283+54C>G (n.2283+54C>G) c.*28+1946C>G (n.*28+1946C>G) c.2148+54C>G (n.2148+54C>G) c.1482+54C>G (n.1482+54C>G) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
7 | g.55174874C>T | CA2714531186 | EGFR | c.2124+54C>T (n.2124+54C>T) c.632+54C>T c.2283+54C>T (n.2283+54C>T) c.*28+1946C>T (n.*28+1946C>T) c.2148+54C>T (n.2148+54C>T) c.1482+54C>T (n.1482+54C>T) | dbSNP |
7 | g.55174875T>A | CA2714960814 | EGFR | c.2124+55T>A (n.2124+55T>A) c.632+55T>A c.2283+55T>A (n.2283+55T>A) c.*28+1947T>A (n.*28+1947T>A) c.2148+55T>A (n.2148+55T>A) c.1482+55T>A (n.1482+55T>A) | dbSNP |
7 | g.55174875T>C | CA2682854922 | EGFR | c.2124+55T>C (n.2124+55T>C) c.632+55T>C c.2283+55T>C (n.2283+55T>C) c.*28+1947T>C (n.*28+1947T>C) c.2148+55T>C (n.2148+55T>C) c.1482+55T>C (n.1482+55T>C) | dbSNP gnomAD v4 |
7 | g.55174878del | CA2682854921 | EGFR | c.2124+58del (n.2124+58del) c.632+58del c.2283+58del (n.2283+58del) c.*28+1950del (n.*28+1950del) c.2148+58del (n.2148+58del) c.1482+58del (n.1482+58del) | gnomAD v4 |