| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 7 | g.55174754_55174771dup | CA135785 | EGFR | c.2217_2234dup (p.Lys745_Glu746insIleProValAlaIleLys) c.*28+1826_*28+1843dup (n.*28+1826_*28+1843dup) c.2082_2099dup (p.Lys700_Glu701insIleProValAlaIleLys) c.2058_2075dup (p.Lys692_Glu693insIleProValAlaIleLys) c.1416_1433dup (p.Lys478_Glu479insIleProValAlaIleLys) | ClinVar dbSNP dbSNP COSMIC COSMIC |
| 7 | g.55174755_55174772dup | CA645550321 | EGFR | c.2218_2235dup (p.Lys745_Glu746insIleProValAlaIleLys) c.*28+1827_*28+1844dup (n.*28+1827_*28+1844dup) c.2083_2100dup (p.Lys700_Glu701insIleProValAlaIleLys) c.2059_2076dup (p.Lys692_Glu693insIleProValAlaIleLys) c.1417_1434dup (p.Lys478_Glu479insIleProValAlaIleLys) | COSMIC |
| 7 | g.55174756_55174773dup | CA645550322 | EGFR | c.2219_2236dup (p.Lys745_Glu746insValProValAlaIleLys) c.*28+1828_*28+1845dup (n.*28+1828_*28+1845dup) c.2084_2101dup (p.Lys700_Glu701insValProValAlaIleLys) c.2060_2077dup (p.Lys692_Glu693insValProValAlaIleLys) c.1418_1435dup (p.Lys478_Glu479insValProValAlaIleLys) | COSMIC |
| 7 | g.55174771_55174772insAACTCCCGTCGCTATCAA | CA645550323 | EGFR | c.2234_2235insAACTCCCGTCGCTATCAA (p.Lys745_Glu746insThrProValAlaIleLys) c.*28+1843_*28+1844insAACTCCCGTCGCTATCAA (n.*28+1843_*28+1844insAACTCCCGTCGCTATCAA) c.2099_2100insAACTCCCGTCGCTATCAA (p.Lys700_Glu701insThrProValAlaIleLys) c.2075_2076insAACTCCCGTCGCTATCAA (p.Lys692_Glu693insThrProValAlaIleLys) c.1433_1434insAACTCCCGTCGCTATCAA (p.Lys478_Glu479insThrProValAlaIleLys) | COSMIC |
| 7 | g.55174766_55174786delinsTATCAAGGAATTAAGAGAAGC | CA1708918302 | EGFR | c.2229_2249delinsTATCAAGGAATTAAGAGAAGC (p.Ala743=) c.*28+1838_*28+1858delinsTATCAAGGAATTAAGAGAAGC (n.*28+1838_*28+1858delinsTATCAAGGAATTAAGAGAAGC) c.2094_2114delinsTATCAAGGAATTAAGAGAAGC (p.Ala698=) c.2070_2090delinsTATCAAGGAATTAAGAGAAGC (p.Ala690=) c.1428_1448delinsTATCAAGGAATTAAGAGAAGC (p.Ala476=) | |
| 7 | g.55174766_55174789delinsAATTAAGA | CA645561481 | EGFR | c.2229_2252delinsAATTAAGA (p.Glu746AsnfsTer15) c.*28+1838_*28+1861delinsAATTAAGA (n.*28+1838_*28+1861delinsAATTAAGA) c.2094_2117delinsAATTAAGA (p.Glu701AsnfsTer15) c.2070_2093delinsAATTAAGA (p.Glu693AsnfsTer15) c.1428_1451delinsAATTAAGA (p.Glu479AsnfsTer15) | COSMIC |
| 7 | g.55174767_55174783delinsCTTAAGAG | CA645561483 | EGFR | c.2230_2246delinsCTTAAGAG (p.Ile744_Glu749delinsLeuLysArg) c.*28+1839_*28+1855delinsCTTAAGAG (n.*28+1839_*28+1855delinsCTTAAGAG) c.2095_2111delinsCTTAAGAG (p.Ile699_Glu704delinsLeuLysArg) c.2071_2087delinsCTTAAGAG (p.Ile691_Glu696delinsLeuLysArg) c.1429_1445delinsCTTAAGAG (p.Ile477_Glu482delinsLeuLysArg) | COSMIC |
| 7 | g.55174767_55174786delinsGTCAA | CA175993 | EGFR | c.2230_2249delinsGTCAA (p.Ile744_Ala750delinsValLys) c.*28+1839_*28+1858delinsGTCAA (n.*28+1839_*28+1858delinsGTCAA) c.2095_2114delinsGTCAA (p.Ile699_Ala705delinsValLys) c.2071_2090delinsGTCAA (p.Ile691_Ala697delinsValLys) c.1429_1448delinsGTCAA (p.Ile477_Ala483delinsValLys) | ClinVar dbSNP COSMIC |
| 7 | g.55174768_55174786delinsTCAAGGAATTAAGAGAAGC | CA1708918305 | EGFR | c.2231_2249delinsTCAAGGAATTAAGAGAAGC (p.Ile744=) c.*28+1840_*28+1858delinsTCAAGGAATTAAGAGAAGC (n.*28+1840_*28+1858delinsTCAAGGAATTAAGAGAAGC) c.2096_2114delinsTCAAGGAATTAAGAGAAGC (p.Ile699=) c.2072_2090delinsTCAAGGAATTAAGAGAAGC (p.Ile691=) c.1430_1448delinsTCAAGGAATTAAGAGAAGC (p.Ile477=) | |
| 7 | g.55174768_55174787delinsTCAAGGAATTAAGAGAAGCA | CA1708918306 | EGFR | c.2231_2250delinsTCAAGGAATTAAGAGAAGCA (p.Ile744=) c.*28+1840_*28+1859delinsTCAAGGAATTAAGAGAAGCA (n.*28+1840_*28+1859delinsTCAAGGAATTAAGAGAAGCA) c.2096_2115delinsTCAAGGAATTAAGAGAAGCA (p.Ile699=) c.2072_2091delinsTCAAGGAATTAAGAGAAGCA (p.Ile691=) c.1430_1449delinsTCAAGGAATTAAGAGAAGCA (p.Ile477=) | |
| 7 | g.55174768_55174789delinsTCAAGGAATTAAGAGAAGCAAC | CA1708918308 | EGFR | c.2231_2252delinsTCAAGGAATTAAGAGAAGCAAC (p.Ile744=) c.*28+1840_*28+1861delinsTCAAGGAATTAAGAGAAGCAAC (n.*28+1840_*28+1861delinsTCAAGGAATTAAGAGAAGCAAC) c.2096_2117delinsTCAAGGAATTAAGAGAAGCAAC (p.Ile699=) c.2072_2093delinsTCAAGGAATTAAGAGAAGCAAC (p.Ile691=) c.1430_1451delinsTCAAGGAATTAAGAGAAGCAAC (p.Ile477=) | |
| 7 | g.55174769_55174786del | CA645561484 | EGFR | c.2232_2249del (p.Lys745_Ala750del) c.*28+1841_*28+1858del (n.*28+1841_*28+1858del) c.2097_2114del (p.Lys700_Ala705del) c.2073_2090del (p.Lys692_Ala697del) c.1431_1448del (p.Lys478_Ala483del) | COSMIC |
| 7 | g.55174769_55174786delinsAAA | CA135794 | EGFR | c.2232_2249delinsAAA (p.Glu746_Ala750del) c.*28+1841_*28+1858delinsAAA (n.*28+1841_*28+1858delinsAAA) c.2097_2114delinsAAA (p.Glu701_Ala705del) c.2073_2090delinsAAA (p.Glu693_Ala697del) c.1431_1448delinsAAA (p.Glu479_Ala483del) | ClinVar dbSNP COSMIC |
| 7 | g.55174769_55174787del | CA180767 | EGFR | c.2232_2250del (p.Lys745HisfsTer15) c.*28+1841_*28+1859del (n.*28+1841_*28+1859del) c.2097_2115del (p.Lys700HisfsTer15) c.2073_2091del (p.Lys692HisfsTer15) c.1431_1449del (p.Lys478HisfsTer15) | ClinVar dbSNP |
| 7 | g.55174769_55174789delinsAAAGTT | CA181093 | EGFR | c.2232_2252delinsAAAGTT (p.Glu746_Thr751delinsLeu) c.*28+1841_*28+1861delinsAAAGTT (n.*28+1841_*28+1861delinsAAAGTT) c.2097_2117delinsAAAGTT (p.Glu701_Thr706delinsLeu) c.2073_2093delinsAAAGTT (p.Glu693_Thr698delinsLeu) c.1431_1451delinsAAAGTT (p.Glu479_Thr484delinsLeu) | ClinVar dbSNP |
| 7 | g.55174771_55174772insAATTCCGGTGGCCATTAA | CA2573051074 | EGFR | c.2234_2235insAATTCCGGTGGCCATTAA (p.Lys745_Glu746insIleProValAlaIleLys) c.*28+1843_*28+1844insAATTCCGGTGGCCATTAA (n.*28+1843_*28+1844insAATTCCGGTGGCCATTAA) c.2099_2100insAATTCCGGTGGCCATTAA (p.Lys700_Glu701insIleProValAlaIleLys) c.2075_2076insAATTCCGGTGGCCATTAA (p.Lys692_Glu693insIleProValAlaIleLys) c.1433_1434insAATTCCGGTGGCCATTAA (p.Lys478_Glu479insIleProValAlaIleLys) | |
| 7 | g.55174770_55174773delinsAAGG | CA1708918310 | EGFR | c.2233_2236delinsAAGG (p.Lys745=) c.*28+1842_*28+1845delinsAAGG (n.*28+1842_*28+1845delinsAAGG) c.2098_2101delinsAAGG (p.Lys700=) c.2074_2077delinsAAGG (p.Lys692=) c.1432_1435delinsAAGG (p.Lys478=) | |
| 7 | g.55174770_55174784del | CA645561485 | EGFR | c.2233_2247del (p.Lys745_Glu749del) c.*28+1842_*28+1856del (n.*28+1842_*28+1856del) c.2098_2112del (p.Lys700_Glu704del) c.2074_2088del (p.Lys692_Glu696del) c.1432_1446del (p.Lys478_Glu482del) | COSMIC |
| 7 | g.55174771A= | CA1708918312 | EGFR | c.2234A= (p.Lys745=) c.*28+1843A= (n.*28+1843A=) c.2099A= (p.Lys700=) c.2075A= (p.Lys692=) c.1433A= (p.Lys478=) | |
| 7 | g.55174771A>C | CA367584143 | EGFR | c.2234A>C (p.Lys745Thr) c.*28+1843A>C (n.*28+1843A>C) c.2099A>C (p.Lys700Thr) c.2075A>C (p.Lys692Thr) c.1433A>C (p.Lys478Thr) | |
| 7 | g.55174771A>G | CA16602542 | EGFR | c.2234A>G (p.Lys745Arg) c.*28+1843A>G (n.*28+1843A>G) c.2099A>G (p.Lys700Arg) c.2075A>G (p.Lys692Arg) c.1433A>G (p.Lys478Arg) | ClinVar dbSNP COSMIC |
| 7 | g.55174771A>T | CA367584144 | EGFR | c.2234A>T (p.Lys745Met) c.*28+1843A>T (n.*28+1843A>T) c.2099A>T (p.Lys700Met) c.2075A>T (p.Lys692Met) c.1433A>T (p.Lys478Met) | |
| 7 | g.55174772_55174774del | CA645561488 | EGFR | c.2235_2237del (p.Glu746del) c.*28+1844_*28+1846del (n.*28+1844_*28+1846del) c.2100_2102del (p.Glu701del) c.2076_2078del (p.Glu693del) c.1434_1436del (p.Glu479del) | ClinVar dbSNP COSMIC |
| 7 | g.55174771_55174780delinsAGGAATTAAG | CA1708918313 | EGFR | c.2234_2243delinsAGGAATTAAG (p.Lys745=) c.*28+1843_*28+1852delinsAGGAATTAAG (n.*28+1843_*28+1852delinsAGGAATTAAG) c.2099_2108delinsAGGAATTAAG (p.Lys700=) c.2075_2084delinsAGGAATTAAG (p.Lys692=) c.1433_1442delinsAGGAATTAAG (p.Lys478=) | |
| 7 | g.55174772_55174783del | CA645561487 | EGFR | c.2235_2246del (p.Glu746_Glu749del) c.*28+1844_*28+1855del (n.*28+1844_*28+1855del) c.2100_2111del (p.Glu701_Glu704del) c.2076_2087del (p.Glu693_Glu696del) c.1434_1445del (p.Glu479_Glu482del) | COSMIC |
| 7 | g.55174771_55174785del | CA645561486 | EGFR | c.2234_2248del (p.Lys745_Ala750delinsThr) c.*28+1843_*28+1857del (n.*28+1843_*28+1857del) c.2099_2113del (p.Lys700_Ala705delinsThr) c.2075_2089del (p.Lys692_Ala697delinsThr) c.1433_1447del (p.Lys478_Ala483delinsThr) | COSMIC |
| 7 | g.55174771_55174785delinsAGGAATTAAGAGAAG | CA1708918314 | EGFR | c.2234_2248delinsAGGAATTAAGAGAAG (p.Lys745=) c.*28+1843_*28+1857delinsAGGAATTAAGAGAAG (n.*28+1843_*28+1857delinsAGGAATTAAGAGAAG) c.2099_2113delinsAGGAATTAAGAGAAG (p.Lys700=) c.2075_2089delinsAGGAATTAAGAGAAG (p.Lys692=) c.1433_1447delinsAGGAATTAAGAGAAG (p.Lys478=) | |
| 7 | g.55174771_55174786delinsAGGAATTAAGAGAAGC | CA1708918311 | EGFR | c.2234_2249delinsAGGAATTAAGAGAAGC (p.Lys745=) c.*28+1843_*28+1858delinsAGGAATTAAGAGAAGC (n.*28+1843_*28+1858delinsAGGAATTAAGAGAAGC) c.2099_2114delinsAGGAATTAAGAGAAGC (p.Lys700=) c.2075_2090delinsAGGAATTAAGAGAAGC (p.Lys692=) c.1433_1448delinsAGGAATTAAGAGAAGC (p.Lys478=) | |
| 7 | g.55174771_55174788delinsAGGAATTAAGAGAAGCAA | CA1708918315 | EGFR | c.2234_2251delinsAGGAATTAAGAGAAGCAA (p.Lys745=) c.*28+1843_*28+1860delinsAGGAATTAAGAGAAGCAA (n.*28+1843_*28+1860delinsAGGAATTAAGAGAAGCAA) c.2099_2116delinsAGGAATTAAGAGAAGCAA (p.Lys700=) c.2075_2092delinsAGGAATTAAGAGAAGCAA (p.Lys692=) c.1433_1450delinsAGGAATTAAGAGAAGCAA (p.Lys478=) | |
| 7 | g.55174771_55174772insAAAATTCCCGTCGCTATC | CA913124879 | EGFR | c.2234_2235insAAAATTCCCGTCGCTATC (p.Lys745_Glu746insLysPheProSerLeuSer) c.*28+1843_*28+1844insAAAATTCCCGTCGCTATC (n.*28+1843_*28+1844insAAAATTCCCGTCGCTATC) c.2099_2100insAAAATTCCCGTCGCTATC (p.Lys700_Glu701insLysPheProSerLeuSer) c.2075_2076insAAAATTCCCGTCGCTATC (p.Lys692_Glu693insLysPheProSerLeuSer) c.1433_1434insAAAATTCCCGTCGCTATC (p.Lys478_Glu479insLysPheProSerLeuSer) | |
| 7 | g.55174772G>A | CA454979445 | EGFR | c.2235G>A (p.Lys745=) c.*28+1844G>A (n.*28+1844G>A) c.2100G>A (p.Lys700=) c.2076G>A (p.Lys692=) c.1434G>A (p.Lys478=) | |
| 7 | g.55174772G>C | CA367584145 | EGFR | c.2235G>C (p.Lys745Asn) c.*28+1844G>C (n.*28+1844G>C) c.2100G>C (p.Lys700Asn) c.2076G>C (p.Lys692Asn) c.1434G>C (p.Lys478Asn) | |
| 7 | g.55174772G>T | CA367584146 | EGFR | c.2235G>T (p.Lys745Asn) c.*28+1844G>T (n.*28+1844G>T) c.2100G>T (p.Lys700Asn) c.2076G>T (p.Lys692Asn) c.1434G>T (p.Lys478Asn) | |
| 7 | g.55174772_55174780del | CA180594 | EGFR | c.2235_2243del (p.Glu746_Arg748del) c.*28+1844_*28+1852del (n.*28+1844_*28+1852del) c.2100_2108del (p.Glu701_Arg703del) c.2076_2084del (p.Glu693_Arg695del) c.1434_1442del (p.Glu479_Arg481del) | ClinVar dbSNP |
| 7 | g.55174772_55174781delinsGGAATTAAGA | CA1708918318 | EGFR | c.2235_2244delinsGGAATTAAGA (p.Lys745=) c.*28+1844_*28+1853delinsGGAATTAAGA (n.*28+1844_*28+1853delinsGGAATTAAGA) c.2100_2109delinsGGAATTAAGA (p.Lys700=) c.2076_2085delinsGGAATTAAGA (p.Lys692=) c.1434_1443delinsGGAATTAAGA (p.Lys478=) | |
| 7 | g.55174772_55174785delinsAATTC | CA180619 | EGFR | c.2235_2248delinsAATTC (p.Glu746_Ala750delinsIlePro) c.*28+1844_*28+1857delinsAATTC (n.*28+1844_*28+1857delinsAATTC) c.2100_2113delinsAATTC (p.Glu701_Ala705delinsIlePro) c.2076_2089delinsAATTC (p.Glu693_Ala697delinsIlePro) c.1434_1447delinsAATTC (p.Glu479_Ala483delinsIlePro) | ClinVar dbSNP COSMIC |
| 7 | g.55174772_55174786del | CA175996 | EGFR | c.2235_2249del (p.Glu746_Ala750del) c.*28+1844_*28+1858del (n.*28+1844_*28+1858del) c.2100_2114del (p.Glu701_Ala705del) c.2076_2090del (p.Glu693_Ala697del) c.1434_1448del (p.Glu479_Ala483del) | ClinVar dbSNP COSMIC |
| 7 | g.55174772_55174787delinsGGAATTAAGAGAAGCA | CA1708918317 | EGFR | c.2235_2250delinsGGAATTAAGAGAAGCA (p.Lys745=) c.*28+1844_*28+1859delinsGGAATTAAGAGAAGCA (n.*28+1844_*28+1859delinsGGAATTAAGAGAAGCA) c.2100_2115delinsGGAATTAAGAGAAGCA (p.Lys700=) c.2076_2091delinsGGAATTAAGAGAAGCA (p.Lys692=) c.1434_1449delinsGGAATTAAGAGAAGCA (p.Lys478=) | |
| 7 | g.55174772_55174788delinsAG | CA645561492 | EGFR | c.2235_2251delinsAG (p.Glu746_Thr751delinsAla) c.*28+1844_*28+1860delinsAG (n.*28+1844_*28+1860delinsAG) c.2100_2116delinsAG (p.Glu701_Thr706delinsAla) c.2076_2092delinsAG (p.Glu693_Thr698delinsAla) c.1434_1450delinsAG (p.Glu479_Thr484delinsAla) | COSMIC |
| 7 | g.55174772_55174788delinsAATTC | CA180803 | EGFR | c.2235_2251delinsAATTC (p.Glu746_Thr751delinsIlePro) c.*28+1844_*28+1860delinsAATTC (n.*28+1844_*28+1860delinsAATTC) c.2100_2116delinsAATTC (p.Glu701_Thr706delinsIlePro) c.2076_2092delinsAATTC (p.Glu693_Thr698delinsIlePro) c.1434_1450delinsAATTC (p.Glu479_Thr484delinsIlePro) | ClinVar dbSNP COSMIC |
| 7 | g.55174772_55174789del | CA645561489 | EGFR | c.2235_2252del (p.Glu746_Thr751del) c.*28+1844_*28+1861del (n.*28+1844_*28+1861del) c.2100_2117del (p.Glu701_Thr706del) c.2076_2093del (p.Glu693_Thr698del) c.1434_1451del (p.Glu479_Thr484del) | COSMIC |
| 7 | g.55174772_55174789delinsAAT | CA645561490 | EGFR | c.2235_2252delinsAAT (p.Glu746_Thr751delinsIle) c.*28+1844_*28+1861delinsAAT (n.*28+1844_*28+1861delinsAAT) c.2100_2117delinsAAT (p.Glu701_Thr706delinsIle) c.2076_2093delinsAAT (p.Glu693_Thr698delinsIle) c.1434_1451delinsAAT (p.Glu479_Thr484delinsIle) | COSMIC |
| 7 | g.55174772_55174789delinsGGAATTAAGAGAAGCAAC | CA1708918316 | EGFR | c.2235_2252delinsGGAATTAAGAGAAGCAAC (p.Lys745=) c.*28+1844_*28+1861delinsGGAATTAAGAGAAGCAAC (n.*28+1844_*28+1861delinsGGAATTAAGAGAAGCAAC) c.2100_2117delinsGGAATTAAGAGAAGCAAC (p.Lys700=) c.2076_2093delinsGGAATTAAGAGAAGCAAC (p.Lys692=) c.1434_1451delinsGGAATTAAGAGAAGCAAC (p.Lys478=) | |
| 7 | g.55174772_55174790delinsGGAATTAAGAGAAGCAACA | CA1708918319 | EGFR | c.2235_2253delinsGGAATTAAGAGAAGCAACA (p.Lys745=) c.*28+1844_*28+1862delinsGGAATTAAGAGAAGCAACA (n.*28+1844_*28+1862delinsGGAATTAAGAGAAGCAACA) c.2100_2118delinsGGAATTAAGAGAAGCAACA (p.Lys700=) c.2076_2094delinsGGAATTAAGAGAAGCAACA (p.Lys692=) c.1434_1452delinsGGAATTAAGAGAAGCAACA (p.Lys478=) | |
| 7 | g.55174772_55174792delinsAAT | CA645561491 | EGFR | c.2235_2255delinsAAT (p.Glu746_Ser752delinsIle) c.*28+1844_*28+1864delinsAAT (n.*28+1844_*28+1864delinsAAT) c.2100_2120delinsAAT (p.Glu701_Ser707delinsIle) c.2076_2096delinsAAT (p.Glu693_Ser699delinsIle) c.1434_1454delinsAAT (p.Glu479_Ser485delinsIle) | COSMIC |
| 7 | g.55174772_55174792delinsAGT | CA2573049007 | EGFR | c.2235_2255delinsAGT (p.Glu746_Ser752delinsVal) c.*28+1844_*28+1864delinsAGT (n.*28+1844_*28+1864delinsAGT) c.2100_2120delinsAGT (p.Glu701_Ser707delinsVal) c.2076_2096delinsAGT (p.Glu693_Ser699delinsVal) c.1434_1454delinsAGT (p.Glu479_Ser485delinsVal) | |
| 7 | g.55174773G>A | CA16602724 | EGFR | c.2236G>A (p.Glu746Lys) c.*28+1845G>A (n.*28+1845G>A) c.2101G>A (p.Glu701Lys) c.2077G>A (p.Glu693Lys) c.1435G>A (p.Glu479Lys) | ClinVar dbSNP COSMIC |
| 7 | g.55174773G>C | CA180723 | EGFR | c.2236G>C (p.Glu746Gln) c.*28+1845G>C (n.*28+1845G>C) c.2101G>C (p.Glu701Gln) c.2077G>C (p.Glu693Gln) c.1435G>C (p.Glu479Gln) | ClinVar dbSNP |
| 7 | g.55174773G= | CA1708918325 | EGFR | c.2236G= (p.Glu746=) c.*28+1845G= (n.*28+1845G=) c.2101G= (p.Glu701=) c.2077G= (p.Glu693=) c.1435G= (p.Glu479=) | |
| 7 | g.55174773G>T | CA367584147 | EGFR | c.2236G>T (p.Glu746Ter) c.*28+1845G>T (n.*28+1845G>T) c.2101G>T (p.Glu701Ter) c.2077G>T (p.Glu693Ter) c.1435G>T (p.Glu479Ter) |