| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 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_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.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.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.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.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.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.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.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.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.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.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.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=) |