Chr Mutation (hg38) CAid Gene Transcript Linkouts
7g.55174754_55174771dupCA135785EGFRc.2217_2234dup (p.Lys745_Glu746insIleProValAlaIleLys)
c.*28+1826_*28+1843dup (p.=)
c.2082_2099dup (p.Lys700_Glu701insIleProValAlaIleLys)
c.2058_2075dup (p.Lys692_Glu693insIleProValAlaIleLys)
c.1416_1433dup (p.Lys478_Glu479insIleProValAlaIleLys)
ClinVar dbSNP dbSNP COSMIC COSMIC
7g.55174755_55174772dupCA645550321EGFRc.2218_2235dup (p.Lys745_Glu746insIleProValAlaIleLys)
c.*28+1827_*28+1844dup (p.=)
c.2083_2100dup (p.Lys700_Glu701insIleProValAlaIleLys)
c.2059_2076dup (p.Lys692_Glu693insIleProValAlaIleLys)
c.1417_1434dup (p.Lys478_Glu479insIleProValAlaIleLys)
COSMIC
7g.55174756_55174773dupCA645550322EGFRc.2219_2236dup (p.Lys745_Glu746insValProValAlaIleLys)
c.*28+1828_*28+1845dup (p.=)
c.2084_2101dup (p.Lys700_Glu701insValProValAlaIleLys)
c.2060_2077dup (p.Lys692_Glu693insValProValAlaIleLys)
c.1418_1435dup (p.Lys478_Glu479insValProValAlaIleLys)
COSMIC
7g.55174771_55174772insAACTCCCGTCGCTATCAACA645550323EGFRc.2234_2235insAACTCCCGTCGCTATCAA (p.Lys745_Glu746insThrProValAlaIleLys)
c.*28+1843_*28+1844insAACTCCCGTCGCTATCAA (p.=)
c.2099_2100insAACTCCCGTCGCTATCAA (p.Lys700_Glu701insThrProValAlaIleLys)
c.2075_2076insAACTCCCGTCGCTATCAA (p.Lys692_Glu693insThrProValAlaIleLys)
c.1433_1434insAACTCCCGTCGCTATCAA (p.Lys478_Glu479insThrProValAlaIleLys)
COSMIC
7g.55174766_55174786delinsTATCAAGGAATTAAGAGAAGCCA1708918302EGFRc.2229_2249delinsTATCAAGGAATTAAGAGAAGC (p.Ala743=)
c.*28+1838_*28+1858delinsTATCAAGGAATTAAGAGAAGC (p.=)
c.2094_2114delinsTATCAAGGAATTAAGAGAAGC (p.Ala698=)
c.2070_2090delinsTATCAAGGAATTAAGAGAAGC (p.Ala690=)
c.1428_1448delinsTATCAAGGAATTAAGAGAAGC (p.Ala476=)
7g.55174766_55174789delinsAATTAAGACA645561481EGFRc.2229_2252delinsAATTAAGA (p.Glu746AsnfsTer15)
c.*28+1838_*28+1861delinsAATTAAGA (p.=)
c.2094_2117delinsAATTAAGA (p.Glu701AsnfsTer15)
c.2070_2093delinsAATTAAGA (p.Glu693AsnfsTer15)
c.1428_1451delinsAATTAAGA (p.Glu479AsnfsTer15)
COSMIC
7g.55174767_55174783delinsCTTAAGAGCA645561483EGFRc.2230_2246delinsCTTAAGAG (p.Ile744_Glu749delinsLeuLysArg)
c.*28+1839_*28+1855delinsCTTAAGAG (p.=)
c.2095_2111delinsCTTAAGAG (p.Ile699_Glu704delinsLeuLysArg)
c.2071_2087delinsCTTAAGAG (p.Ile691_Glu696delinsLeuLysArg)
c.1429_1445delinsCTTAAGAG (p.Ile477_Glu482delinsLeuLysArg)
COSMIC
7g.55174767_55174786delinsGTCAACA175993EGFRc.2230_2249delinsGTCAA (p.Ile744_Ala750delinsValLys)
c.*28+1839_*28+1858delinsGTCAA (p.=)
c.2095_2114delinsGTCAA (p.Ile699_Ala705delinsValLys)
c.2071_2090delinsGTCAA (p.Ile691_Ala697delinsValLys)
c.1429_1448delinsGTCAA (p.Ile477_Ala483delinsValLys)
ClinVar dbSNP COSMIC
7g.55174768_55174786delinsTCAAGGAATTAAGAGAAGCCA1708918305EGFRc.2231_2249delinsTCAAGGAATTAAGAGAAGC (p.Ile744=)
c.*28+1840_*28+1858delinsTCAAGGAATTAAGAGAAGC (p.=)
c.2096_2114delinsTCAAGGAATTAAGAGAAGC (p.Ile699=)
c.2072_2090delinsTCAAGGAATTAAGAGAAGC (p.Ile691=)
c.1430_1448delinsTCAAGGAATTAAGAGAAGC (p.Ile477=)
7g.55174768_55174787delinsTCAAGGAATTAAGAGAAGCACA1708918306EGFRc.2231_2250delinsTCAAGGAATTAAGAGAAGCA (p.Ile744=)
c.*28+1840_*28+1859delinsTCAAGGAATTAAGAGAAGCA (p.=)
c.2096_2115delinsTCAAGGAATTAAGAGAAGCA (p.Ile699=)
c.2072_2091delinsTCAAGGAATTAAGAGAAGCA (p.Ile691=)
c.1430_1449delinsTCAAGGAATTAAGAGAAGCA (p.Ile477=)
7g.55174768_55174789delinsTCAAGGAATTAAGAGAAGCAACCA1708918308EGFRc.2231_2252delinsTCAAGGAATTAAGAGAAGCAAC (p.Ile744=)
c.*28+1840_*28+1861delinsTCAAGGAATTAAGAGAAGCAAC (p.=)
c.2096_2117delinsTCAAGGAATTAAGAGAAGCAAC (p.Ile699=)
c.2072_2093delinsTCAAGGAATTAAGAGAAGCAAC (p.Ile691=)
c.1430_1451delinsTCAAGGAATTAAGAGAAGCAAC (p.Ile477=)
7g.55174769_55174786delCA645561484EGFRc.2232_2249del (p.Lys745_Ala750del)
c.*28+1841_*28+1858del (p.=)
c.2097_2114del (p.Lys700_Ala705del)
c.2073_2090del (p.Lys692_Ala697del)
c.1431_1448del (p.Lys478_Ala483del)
COSMIC
7g.55174769_55174786delinsAAACA135794EGFRc.2232_2249delinsAAA (p.Glu746_Ala750del)
c.*28+1841_*28+1858delinsAAA (p.=)
c.2097_2114delinsAAA (p.Glu701_Ala705del)
c.2073_2090delinsAAA (p.Glu693_Ala697del)
c.1431_1448delinsAAA (p.Glu479_Ala483del)
ClinVar dbSNP COSMIC
7g.55174769_55174787delCA180767EGFRc.2232_2250del (p.Lys745HisfsTer15)
c.*28+1841_*28+1859del (p.=)
c.2097_2115del (p.Lys700HisfsTer15)
c.2073_2091del (p.Lys692HisfsTer15)
c.1431_1449del (p.Lys478HisfsTer15)
ClinVar dbSNP
7g.55174769_55174789delinsAAAGTTCA181093EGFRc.2232_2252delinsAAAGTT (p.Glu746_Thr751delinsLeu)
c.*28+1841_*28+1861delinsAAAGTT (p.=)
c.2097_2117delinsAAAGTT (p.Glu701_Thr706delinsLeu)
c.2073_2093delinsAAAGTT (p.Glu693_Thr698delinsLeu)
c.1431_1451delinsAAAGTT (p.Glu479_Thr484delinsLeu)
ClinVar dbSNP
7g.55174770A>CCA367584141EGFRc.2233A>C (p.Lys745Gln)
c.*28+1842A>C (p.=)
c.2098A>C (p.Lys700Gln)
c.2074A>C (p.Lys692Gln)
c.1432A>C (p.Lys478Gln)
7g.55174770A>GCA367584142EGFRc.2233A>G (p.Lys745Glu)
c.*28+1842A>G (p.=)
c.2098A>G (p.Lys700Glu)
c.2074A>G (p.Lys692Glu)
c.1432A>G (p.Lys478Glu)
7g.55174770A>TCA367584140EGFRc.2233A>T (p.Lys745Ter)
c.*28+1842A>T (p.=)
c.2098A>T (p.Lys700Ter)
c.2074A>T (p.Lys692Ter)
c.1432A>T (p.Lys478Ter)
7g.55174770_55174773delinsAAGGCA1708918310EGFRc.2233_2236delinsAAGG (p.Lys745=)
c.*28+1842_*28+1845delinsAAGG (p.=)
c.2098_2101delinsAAGG (p.Lys700=)
c.2074_2077delinsAAGG (p.Lys692=)
c.1432_1435delinsAAGG (p.Lys478=)
7g.55174770_55174784delCA645561485EGFRc.2233_2247del (p.Lys745_Glu749del)
c.*28+1842_*28+1856del (p.=)
c.2098_2112del (p.Lys700_Glu704del)
c.2074_2088del (p.Lys692_Glu696del)
c.1432_1446del (p.Lys478_Glu482del)
COSMIC
7g.55174771A=CA1708918312EGFRc.2234A= (p.Lys745=)
c.*28+1843A= (p.=)
c.2099A= (p.Lys700=)
c.2075A= (p.Lys692=)
c.1433A= (p.Lys478=)
7g.55174771A>CCA367584143EGFRc.2234A>C (p.Lys745Thr)
c.*28+1843A>C (p.=)
c.2099A>C (p.Lys700Thr)
c.2075A>C (p.Lys692Thr)
c.1433A>C (p.Lys478Thr)
7g.55174771A>GCA16602542EGFRc.2234A>G (p.Lys745Arg)
c.*28+1843A>G (p.=)
c.2099A>G (p.Lys700Arg)
c.2075A>G (p.Lys692Arg)
c.1433A>G (p.Lys478Arg)
ClinVar dbSNP COSMIC
7g.55174771A>TCA367584144EGFRc.2234A>T (p.Lys745Met)
c.*28+1843A>T (p.=)
c.2099A>T (p.Lys700Met)
c.2075A>T (p.Lys692Met)
c.1433A>T (p.Lys478Met)
7g.55174772_55174774delCA645561488EGFRc.2235_2237del (p.Glu746del)
c.*28+1844_*28+1846del (p.=)
c.2100_2102del (p.Glu701del)
c.2076_2078del (p.Glu693del)
c.1434_1436del (p.Glu479del)
ClinVar dbSNP COSMIC
7g.55174771_55174780delinsAGGAATTAAGCA1708918313EGFRc.2234_2243delinsAGGAATTAAG (p.Lys745=)
c.*28+1843_*28+1852delinsAGGAATTAAG (p.=)
c.2099_2108delinsAGGAATTAAG (p.Lys700=)
c.2075_2084delinsAGGAATTAAG (p.Lys692=)
c.1433_1442delinsAGGAATTAAG (p.Lys478=)
7g.55174772_55174783delCA645561487EGFRc.2235_2246del (p.Glu746_Glu749del)
c.*28+1844_*28+1855del (p.=)
c.2100_2111del (p.Glu701_Glu704del)
c.2076_2087del (p.Glu693_Glu696del)
c.1434_1445del (p.Glu479_Glu482del)
COSMIC
7g.55174771_55174785delCA645561486EGFRc.2234_2248del (p.Lys745_Ala750delinsThr)
c.*28+1843_*28+1857del (p.=)
c.2099_2113del (p.Lys700_Ala705delinsThr)
c.2075_2089del (p.Lys692_Ala697delinsThr)
c.1433_1447del (p.Lys478_Ala483delinsThr)
COSMIC
7g.55174771_55174785delinsAGGAATTAAGAGAAGCA1708918314EGFRc.2234_2248delinsAGGAATTAAGAGAAG (p.Lys745=)
c.*28+1843_*28+1857delinsAGGAATTAAGAGAAG (p.=)
c.2099_2113delinsAGGAATTAAGAGAAG (p.Lys700=)
c.2075_2089delinsAGGAATTAAGAGAAG (p.Lys692=)
c.1433_1447delinsAGGAATTAAGAGAAG (p.Lys478=)
7g.55174771_55174786delinsAGGAATTAAGAGAAGCCA1708918311EGFRc.2234_2249delinsAGGAATTAAGAGAAGC (p.Lys745=)
c.*28+1843_*28+1858delinsAGGAATTAAGAGAAGC (p.=)
c.2099_2114delinsAGGAATTAAGAGAAGC (p.Lys700=)
c.2075_2090delinsAGGAATTAAGAGAAGC (p.Lys692=)
c.1433_1448delinsAGGAATTAAGAGAAGC (p.Lys478=)
7g.55174771_55174788delinsAGGAATTAAGAGAAGCAACA1708918315EGFRc.2234_2251delinsAGGAATTAAGAGAAGCAA (p.Lys745=)
c.*28+1843_*28+1860delinsAGGAATTAAGAGAAGCAA (p.=)
c.2099_2116delinsAGGAATTAAGAGAAGCAA (p.Lys700=)
c.2075_2092delinsAGGAATTAAGAGAAGCAA (p.Lys692=)
c.1433_1450delinsAGGAATTAAGAGAAGCAA (p.Lys478=)
7g.55174771_55174772insAAAATTCCCGTCGCTATCCA913124879EGFRc.2234_2235insAAAATTCCCGTCGCTATC (p.Lys745_Glu746insLysPheProSerLeuSer)
c.*28+1843_*28+1844insAAAATTCCCGTCGCTATC (p.=)
c.2099_2100insAAAATTCCCGTCGCTATC (p.Lys700_Glu701insLysPheProSerLeuSer)
c.2075_2076insAAAATTCCCGTCGCTATC (p.Lys692_Glu693insLysPheProSerLeuSer)
c.1433_1434insAAAATTCCCGTCGCTATC (p.Lys478_Glu479insLysPheProSerLeuSer)
7g.55174772G>ACA454979445EGFRc.2235G>A (p.Lys745=)
c.*28+1844G>A (p.=)
c.2100G>A (p.Lys700=)
c.2076G>A (p.Lys692=)
c.1434G>A (p.Lys478=)
7g.55174772G>CCA367584145EGFRc.2235G>C (p.Lys745Asn)
c.*28+1844G>C (p.=)
c.2100G>C (p.Lys700Asn)
c.2076G>C (p.Lys692Asn)
c.1434G>C (p.Lys478Asn)
7g.55174772G>TCA367584146EGFRc.2235G>T (p.Lys745Asn)
c.*28+1844G>T (p.=)
c.2100G>T (p.Lys700Asn)
c.2076G>T (p.Lys692Asn)
c.1434G>T (p.Lys478Asn)
7g.55174772_55174780delCA180594EGFRc.2235_2243del (p.Glu746_Arg748del)
c.*28+1844_*28+1852del (p.=)
c.2100_2108del (p.Glu701_Arg703del)
c.2076_2084del (p.Glu693_Arg695del)
c.1434_1442del (p.Glu479_Arg481del)
ClinVar dbSNP
7g.55174772_55174781delinsGGAATTAAGACA1708918318EGFRc.2235_2244delinsGGAATTAAGA (p.Lys745=)
c.*28+1844_*28+1853delinsGGAATTAAGA (p.=)
c.2100_2109delinsGGAATTAAGA (p.Lys700=)
c.2076_2085delinsGGAATTAAGA (p.Lys692=)
c.1434_1443delinsGGAATTAAGA (p.Lys478=)
7g.55174772_55174785delinsAATTCCA180619EGFRc.2235_2248delinsAATTC (p.Glu746_Ala750delinsIlePro)
c.*28+1844_*28+1857delinsAATTC (p.=)
c.2100_2113delinsAATTC (p.Glu701_Ala705delinsIlePro)
c.2076_2089delinsAATTC (p.Glu693_Ala697delinsIlePro)
c.1434_1447delinsAATTC (p.Glu479_Ala483delinsIlePro)
ClinVar dbSNP COSMIC
7g.55174772_55174786delCA175996EGFRc.2235_2249del (p.Glu746_Ala750del)
c.*28+1844_*28+1858del (p.=)
c.2100_2114del (p.Glu701_Ala705del)
c.2076_2090del (p.Glu693_Ala697del)
c.1434_1448del (p.Glu479_Ala483del)
ClinVar dbSNP COSMIC
7g.55174772_55174787delinsGGAATTAAGAGAAGCACA1708918317EGFRc.2235_2250delinsGGAATTAAGAGAAGCA (p.Lys745=)
c.*28+1844_*28+1859delinsGGAATTAAGAGAAGCA (p.=)
c.2100_2115delinsGGAATTAAGAGAAGCA (p.Lys700=)
c.2076_2091delinsGGAATTAAGAGAAGCA (p.Lys692=)
c.1434_1449delinsGGAATTAAGAGAAGCA (p.Lys478=)
7g.55174772_55174788delinsAGCA645561492EGFRc.2235_2251delinsAG (p.Glu746_Thr751delinsAla)
c.*28+1844_*28+1860delinsAG (p.=)
c.2100_2116delinsAG (p.Glu701_Thr706delinsAla)
c.2076_2092delinsAG (p.Glu693_Thr698delinsAla)
c.1434_1450delinsAG (p.Glu479_Thr484delinsAla)
COSMIC
7g.55174772_55174788delinsAATTCCA180803EGFRc.2235_2251delinsAATTC (p.Glu746_Thr751delinsIlePro)
c.*28+1844_*28+1860delinsAATTC (p.=)
c.2100_2116delinsAATTC (p.Glu701_Thr706delinsIlePro)
c.2076_2092delinsAATTC (p.Glu693_Thr698delinsIlePro)
c.1434_1450delinsAATTC (p.Glu479_Thr484delinsIlePro)
ClinVar dbSNP COSMIC
7g.55174772_55174789delCA645561489EGFRc.2235_2252del (p.Glu746_Thr751del)
c.*28+1844_*28+1861del (p.=)
c.2100_2117del (p.Glu701_Thr706del)
c.2076_2093del (p.Glu693_Thr698del)
c.1434_1451del (p.Glu479_Thr484del)
COSMIC
7g.55174772_55174789delinsAATCA645561490EGFRc.2235_2252delinsAAT (p.Glu746_Thr751delinsIle)
c.*28+1844_*28+1861delinsAAT (p.=)
c.2100_2117delinsAAT (p.Glu701_Thr706delinsIle)
c.2076_2093delinsAAT (p.Glu693_Thr698delinsIle)
c.1434_1451delinsAAT (p.Glu479_Thr484delinsIle)
COSMIC
7g.55174772_55174789delinsGGAATTAAGAGAAGCAACCA1708918316EGFRc.2235_2252delinsGGAATTAAGAGAAGCAAC (p.Lys745=)
c.*28+1844_*28+1861delinsGGAATTAAGAGAAGCAAC (p.=)
c.2100_2117delinsGGAATTAAGAGAAGCAAC (p.Lys700=)
c.2076_2093delinsGGAATTAAGAGAAGCAAC (p.Lys692=)
c.1434_1451delinsGGAATTAAGAGAAGCAAC (p.Lys478=)
7g.55174772_55174790delinsGGAATTAAGAGAAGCAACACA1708918319EGFRc.2235_2253delinsGGAATTAAGAGAAGCAACA (p.Lys745=)
c.*28+1844_*28+1862delinsGGAATTAAGAGAAGCAACA (p.=)
c.2100_2118delinsGGAATTAAGAGAAGCAACA (p.Lys700=)
c.2076_2094delinsGGAATTAAGAGAAGCAACA (p.Lys692=)
c.1434_1452delinsGGAATTAAGAGAAGCAACA (p.Lys478=)
7g.55174772_55174792delinsAATCA645561491EGFRc.2235_2255delinsAAT (p.Glu746_Ser752delinsIle)
c.*28+1844_*28+1864delinsAAT (p.=)
c.2100_2120delinsAAT (p.Glu701_Ser707delinsIle)
c.2076_2096delinsAAT (p.Glu693_Ser699delinsIle)
c.1434_1454delinsAAT (p.Glu479_Ser485delinsIle)
COSMIC
7g.55174773G>ACA16602724EGFRc.2236G>A (p.Glu746Lys)
c.*28+1845G>A (p.=)
c.2101G>A (p.Glu701Lys)
c.2077G>A (p.Glu693Lys)
c.1435G>A (p.Glu479Lys)
ClinVar dbSNP COSMIC
7g.55174773G>CCA180723EGFRc.2236G>C (p.Glu746Gln)
c.*28+1845G>C (p.=)
c.2101G>C (p.Glu701Gln)
c.2077G>C (p.Glu693Gln)
c.1435G>C (p.Glu479Gln)
ClinVar dbSNP
7g.55174773G=CA1708918325EGFRc.2236G= (p.Glu746=)
c.*28+1845G= (p.=)
c.2101G= (p.Glu701=)
c.2077G= (p.Glu693=)
c.1435G= (p.Glu479=)

Number of alleles fetched